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Revision as of 15:59, 12 October 2014

Notebook: June

02.06.2014

13.56 Make Gly Stocks of the following strains

Aim: Have gly stocks

Dh5a pRSII426 –hGRa
Dh5a piGEM010 (p003 + Tag 21)
Dh5a piGEM015 (p004 + Tag 23)
Dh5a piGEM014 (p003 + Tag 22)
Dh5a piGEM008 (p002 + Tag 22)
Dh5a piGEM007 (p002 + Tag 21)
Dh5a piGEM011 (p003 + Tag 22)
Dh5a piGEM012 (p003 + Tag 23)

13.57 Mini Prep of cultures inoculated on Friday 30.5. Nose Plasmids

piGEM010 = 22ng/µl
piGEM013 = 46 ng/µl
piGEM 009 = 13 ng/µl

low concentration: new transformation to gain more plasmid DNA
Strain: new competent E. coli XL1-blue

15.50 Miniprep of pMAD-fla-cup1-1 for miniprep

The miniprep was performed accoding to the miniprep protocol.

Concentration 40 ng/µL
low concentration: new transformation to gain more plasmid DNA should be done
Strain: new competent E. coli XL1-blue

13.58 Bacillus Trafo with all Nose Plasmids containing one/no Degradation Tag

Aim: Create Bacillus subtilis strain 3610 containing the following plasmids: piGEM002 to 004 and piGEM007 to 016

Add 5µl plasmid DNA and incubate for 30 min at 37°C, LB plate with 5 ng/µL Cm (prepared freshly)

13.59 Inoculation of Bacillus subtilis wildtype (3610), gfp (186) and silver nose

Aim: Aim: MTA tomorrow to check out what concentrations of Ag+ are still okay for the cells to survive, since 1mM until 10µM was too high and the cells died

Starting from 1 mM 8 dilutions have been prepared

18.1 Tumor Terminator - Dilution of Plasmid

Aim: Creating a stock solution

We received the synthetized DARPin-gene in a pEC-A2 vector with spe1 restriction sites at the 5’- and 3’-site at an amount of 2,7µg plasmid in the tube.

A stock solution was created by adding 27µl water to the tube.

Concentration of stock solution = 100 ng/µl

A 1:10 dilution was created by using 1µl of stock solution adding 9µL of water to an end concentration of 10ng/µl.

Concentration of stock dilution = 10 ng/µl.

18.2 Transformation of DARPin-gene in plasmid into E.Coli XL1-Blue

Aim: Transforming pEX-A2 plasmid with DARPin-gene into E.Coli for amplification of the Gene.

1µl of the 1:10 stock dilution were used for transformation of E. Coli XL1-Blue

03.06.2014

18.3 Miniprep of DARPin-gene in plasmid in E.Coli XL1-Blue

Aim: Receiving a higher amount of plasmid for further experiments.

3 x6ml LB-Amp were inoculated with clones from the successful transformed plate (18.2) and incubated at 37°C overnight.

13.60 Microtiter plate assay with wildtype, gfp strain 186 and silver nose

Aim: MTA tomorrow to check out what concentrations of Ag+ are still okay for the cells to survive, since 1mM until 10 µM was too high and the cells died

Starting from 1 mM 8 dilutions have been prepared.
In the beginning Minimalmedium S750 has been prepared with 0.5‰ Xylose
In the wells the following mix was added to a total volume of 150 µl:
135µl of MM (90‰) and Silver solution (10‰)
15µl of cells
Finally 70 µl are added to avoid evaporation of the medium

Incubation for appr. 24h at 37°C shaking (Viktor AG Waldminghaus)

13.61 Checking Bacillus Trafo with all Nose Plasmids containing one/no Degradation Tag

Every transformation plate showed a huge growth of bacillus without single colonies. After one day of incubation this seems to be an unrealistic growth which is why we plan to repeat the transformation after checking the growth of the Bacillus subtilis Wildtype 3610 on LB-CM plate with 5 µg/ml CM.

13.62 Checking Bacillus Trafo Wildtype 3610

Aim: check if wildtype has a resistance against CM or if the plates are not effective/ made wrong

Bacillus subtilis Wildtype 3610 was plated on LB-CM plate with 5 µg/ml CM and incubated overnight at 37°C.

15.51 Making selection plates for clean deletions – integration of pMAD-construct into Bacillus subtilis chromosome

Aim: For the integration of the constructs we cloned into pMAD many steps of a special selection are necessary. For the protocoll we received from Florian Altegoer MLS and MLS X-gal plates have to be used.

Antibiotics and chemicals:

Erythromycin 4 mg/ml
Lincomycin 25mg/ml
X-Gal 100mg/ml

For MLS selection plates Erythromycin with 1mg/ml were needed. Therefore the 4 mg/mL stock solution was diluted 1:4 by mixing 400 µl Eryhtomycin with 1200 µl of 70° ethanol.

3 types of plates were made:

1. MLS selectin: 800 mL LB agar + 800 µl Eryhtromycin + 800 µl Lincomycin
2. MLS X-Gal: 800 mL LB agar + 800 µl Eryhtromycin + 800 µl Lincomycin + 800 µl X-Gal
3. X-Gal: 800 mL LB agar + 800 µL X-Gal

About 120 plates were stored at the 4°C room at AG Graumann labs.

04.06.2014

18.4 Miniprep of DARPin-gene in plasmid in E.Coli XL1-Blue

Plasmid pEX-A2 + DARPinEc1	Concentration after prep (ng/µl)
Clone 1	398,7
Clone 2	340
Clone 3	309

15.52 Sequencing pMAD-fla-cup1-1

Aim: Checking the correct insertion of the metallothionein-domain into the hag –flank construct

Making a pre-mix for Eurofins MWG prepairing the sequencing. Primers from Florian Altegoer were used:

Flo83- Hag11_fw 1:10 with 1µl primer and 9µl water
Flo86- Hag12_rv 1:10 with 1µl primer and 9µl water

	Pre-mix 1 (µL)	Pre-mix 2 (µL)
piGEM-016 pMAD-cup1-1 40ng/µL	10	10
Flo83- Hag11_fw	2	-
Flo86- Hag12_rv	-	2
Total Volume	12	12

Label	Pre-mix 1	Primer
AGB0023375	Pre-mix 1	Flo83 – Hag11_fw
AGB0023374	Pre-mix 1	Flo86 - Hag12_rv

13.62 Checking Bacillus Trafo Wildtype 3610

Aim: check if wildtype has a resistance against CM or if the plates are not effective/ made wrong

Result: Bacillus subtilis Wildtype 3610 grew on the CM plate which shows us that there has to be a mistake in making the LB-CM plates or the WT has a resistance.

In order to exclude the false making of plates new ones were made with new CM-stocks with 25 mg/ml and 5 mg/ml.

3 aliquots of competent B.s. WT3610 were plated on new LB-CM plates and incubated at 37°C.

18.5 Spe1 restriction of DARPin-gene in pEX-A2 & pMAD-hag-flank (piGEM-005)

Aim: Receiving iGEM-005 as linearized vector for cloning the DARPin gene with Spe1 sites into pMAD-fla (iGEM-005)

Restriction	pEX-A2-DARPin digest (µl)	pMAD-Hag-Flank digest (µl)	Spe1-Mastermix
pEX-A2+DARPin (398 µg/µL)	15 = ca. 6µg	-	-
pMAD-Fla (114 µg/µL)	-	10= ca. 1,14 µg	-
SpeI	-	-	1,5
CutSmart-Buffer (10x)	-	-	2
H2O	-	-	16,5
Mastermix	5	10	-
Total	20	20	20

Incubation at 37°C for 2h and heat shock at 81°C for 5 min. After that the pMAD-Hag-Flank-Construct was purified with the OMEGA gel extraction kit according to the protocol.

c(digested piGEM-005)= 4 ng/µl

13.62 Checking Bacillus Trafo Wildtype 3610

Aim: check if wildtype has a resistance against CM or if the plates are not effective/ made wrong

Result: Bacillus subtilis Wildtype 3610 grew on the CM plate. We have already repeated making plates so it might be that the WT has got a resistance while making it competent. New WT from Florian Altegoer was plated on 2 CM plates with 5µg/µL (old and new one) and 2x LB plates from gly stocks.

Incubation at 37°C overnight.

06.06.2014

19. Crystallization of flagellin

In order to cristallize flagellin with a domain it is necessary to produce the protein by E.Coli in a high concentration. For that aim the Fla-construct will be amplificated out of pet24d which includes a domain. For elimination of the flanks a PCR has to be perfomed which just amplificates Hag with Domain and creates Nco1 and BamH1 restriction sites. After purification and digest with Nco/Bam the fragment can be ligated into Nco/Bam digested pet24d . After transformation the synthesis can be induced by IPTG.

19.1 Eliminiation of flanks from Fla-construct including cup1-1out of pet24d

Aim: Preparation for using pet24d as expression vector for flagellin

The flagellin construct was amplificated with Primer 95 and 54 from Florian Altegoer which allow the amplification of the construct with cup1-1 without flanks (just Hag) including Nco1 & BamH1 restriction sites.
Template dilution 1:10:
1µL pet24d-cup1-1 was mixed with 9 µL to an 1:10 dilution of 16,3 ng/µL
Primer dilution 1:10:
Primers 95 & 54 from Florian Altegoer were diluted 1:10 by mixing 10µL of primers with 90µL milipore water each.

Mix [µl]	1 attempt with phusion	One attempt with Q5 mastermix
Pet24d-cup1-1 1:10 dilution	1	1
Primer 54Flo	1	1
Primer 56Flo	1	1
Phusion	1	-
Phusion Buffer 5x	10	-
dNTP Mix	1	-
Water	35	22
Q5 Mastermix	-	25
Total Volume	50	20

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	30 sec
4	72	2 min
5	Go To 2	30x
6	72	4min
7	8	infinite

PCR was run overnight.

19.2 Restriction digest of pet24d with Nco1 and BamH1

Aim: Creating Nco/ Bam restriction sites in pet24d for cloning PCR fragments amplified with primers flo56 and flo54 which contain Nco/Bam sites as well.

Prepped pet24d was cut with Nco1 and BamH1 in order to create restriction sites for ligating the Flagellin/ Hag-Domain fragments into the vector. The Hag-fragments which were amplified via PCR with primers flo54 and 56 contain Nco1/ BamH1 restriction sites for that purpose as well.

Component	Volume [µl]
Pet24d (148 ng/µL)	7
Cutsmart 10x	2
Nco1	0,5
BamH1	0,5
Water	10
Total Volume	20

Incubation for 1h at 37°C and heat shocked at 80°C.

15.52 Miniprep of different plasmids

Aim: Receiving more plasmid DNA for further experiments

Colonies were picked from plates and 8ml LB with necessary antibiotics each inoculated, followed by incubation at 37°C overnight.

Clones were picked from plates with plasmids:

Pet24d-Fla-Cup1-1 (piGEM-006)
pMAD-Hag-Flank (piGEM-005)
pMAD-Hag-Flank -Cup1-1 (piGEM-016)
pEX-A2+DARPin (piGEM-017)

07.062014

15.53 Sequencing pMAD-fla-cup1-1

The sequencing showed the correct insertion of the cup-1-1 gene into the hag-flank construct but contained a stop codon which was not removed by the used reverse primer. Unfortunately we used primers for amplification of the whole cup1-1 gene and not just for the truncated gene coding for the metallothionein domain only. Therefore new primers had to be designed an the gibson assembly for integration of the metallothionein domain into pMAD and pet24d has to be repeated.

18.6 gel extraction & purification of DARPin gene

Aim: Receiving DARPin gene with spe1 sites for ligation into linearized piGEM-005

The with Spe1 digested pEX-A2 was purified via electrophoresis with an 1% agarose gel in order to divide pEX-A2 backbone and the DARPin gene (489 bp). The digest attempt was splitted and loaded into two pockets to be sure not to overload the gel. The correct bands were cut out and the DNA fragment was rescued according to the protocol of our OMEGA gel extraction kit.

Expected bands:
DARPin gene: 489 bp
pEX-A2 backbone: 1961bp
The concentration after gel extraction: 9 ng/µl

18.7 Ligation of DARPin gene and linearized piGEM-005

Aim: Ligation of DARPin- (from 18.6) into Spe1 cut piGEM-005 from 18.5 for integration of the DARPin-Flagellin construct into Bacillus subtilis chromosome

The DARPin gene with Spe1 sites was used as insert for the ligation into linearized pMAD (from 18.5) which contains the designed Spe1 site. The ligation attempt was done twofold and calculated by the Ligation Calculator from the iGEM-Team Texas in 2011:

Component	Volume [µl]
Insert (DARPin, c= 9 ng/µL)	2
Vector (piGEM-005, c=4ng/µL)	10
Ligase-Buffer 10x	2
T4 Ligase	1
Milipore water	5
Total Volume	20

Incubation was performed overnight at room temperature.

13.63 checking Bacillus WT 3610 growth on 5µg/µL CM

Aim: check if wildtype has a resistance against CM

Result: Bacillus subtilis Wildtype 3610 grew on the CM plate.

In order to make out if a selection is possible WT3610 was plated out from an LB plate (13.62) on 25 ng/ µL CM to check were Bacillus CM threshold is.

Incubation at 30°C over the weekend.

08.06.2014

18.8 new Spe1 restriction of DARPin-gene in pEX-A2 & pMAD-hag-flank (piGEM-005)

Aim: Receiving new insert and vector in case of an unsuccessful ligation for further attempts.

Restriction	pEX-A2-DARPin digest (µl)	pMAD-Hag-Flank digest (µl)	Spe1-Mastermix
pEX-A2+DARPin (398 µg/µL)	10 = ca. 4µg	-	-
pMAD-Fla (150 µg/µL)	-	7= ca. 1 µg	-
SpeI	-	-	1
CutSmart-Buffer (10x)	-	-	2,5
Water	-	-	21,5
Mastermix	10	13	-
Total Volume	20	20	25

Incubation was performed for 2h at 37°C and heat inactivated at 80°C for 5 minutes.

18.9 Transformation of overnight ligation from 18.7

The whole 20µL attempt from the overnight ligations were transformed into E.Coli XL1-Blue and plated on LB-Amp plates. Additionally a negative control was created by transforming 1µL Spe1 cut piGEM-005 into E.Coli XL1-Blue as well.

18.10 Gel extraction for isolation of DARPin gene out of pEX-A2

Aim: Receiving new insert in case of an unsuccessful ligation for further attempts like in 18.6

The with Spe1 digested pEX-A2 was purified via electrophoresis with an 1% agarose gel like in 18.6. The band correct bands were cut out and the DNA fragment was rescued according to the protocol of our OMEGA gel extraction kit.

Expected bands:
DARPin gene: 489 bp
pEX-A2 backbone: 1961bp
The concentration after gel extraction: 10 ng/µl

09.06.2014

18.12 Checking Transformation of overnight ligation from 18.7

Plate	Amount of colonies
Negative control	6
Ligation attempt 1	7
Ligation attempt 2	0

18.13 Checking success of ligation via cPCR

Aim: A cPCR with the primers 54 and 56 shows the success of ligation by amplification of the Hag-construct.

In order to check the positive insertion of the DARPin gene into pMAD a PCR amplification with primers 54 and 56 for the flagellin should generate an ca. 1500 bp fragment on the gel. Negative clones would show still just a 1000 bp band because of the amplification of the Hag-Spe1 site construct. The picked clones were transferred on a new LB-amp plate.

Mix	Master-Mix for 7 attempts (µL)	Mix for PCR attempt (µL)
Colony	-	part of a colony
Primer Flo 54	3,5	-
Primer Flo 56	3,5	-
Phusion	7	-
Phusion Buffer 5x	28	-
dNTP Mix	3,5	-
Water	94,5	-
Mastermix	-	20
Total Volume	140	20

Expected bands:
Hag-DARPin-construct: ca. 1500 bp

The gel shows bands at 1000 which means that the clones contain just relegated pMAD vector and are all negative. The ligation had to be repeated.

18.14 Dephosphorylation of linearized piGEM-005

Aim: Dephosphorylation of 5’-end with antarctic phosphatase in order to decrease the religation of the linearized piGEM-005 from 18.8

The cut Spe1 cut piGEM-005 was dephosporylated at the 5’-end with Antarctic phosphatase to prevent the vector from relegation.

Component	Volume [µl]
Vector (piGEM-005, c=148 ng/µL)	20 (=ca. 2 µg)
Antarctic phos.-Buffer 10x	3
Antarctic phosphatase	1
Milipore Water	6
Total Volume	30

The sample was incubated for 1h at 37°C at heat inactivated at 70°C for 10minutes.

18. new ligation of linearized/ dephosphorylized piGEM-005 & DARPin gene

Aim: Dephosphorylation piGEM-005 was ligated with extracted DARPin gene again

Because of the negative colony PCR from 18.13 a new ligation with dephosphorylized piGEM-005 from 18.14 and new extracted DARPin gene from 18.10 was performed in 2 attempts.

Component	Volume [µl]
Insert (DARPin, c= 10 ng/µL)	12,4
Vector (piGEM-005, c= 148 ng/µL)	4,6
Ligase-Buffer 10x	2
T4 Ligase	1
Milipore Water	5
Total Volume	20

Incubation 3h at room temperature

18.16 Transformation of overnight ligation from 18.15

The whole 20µL attempt from the ligations (18.15) were transformed into E.Coli XL1-Blue and plated on LB-Amp plates. Additionally a negative control was created by transforming 1µL Spe1 cut piGEM-005 into E.Coli XL1-Blue as well.

13.64 checking Bacillus WT 3610 growth on 5, 10 & 15 µg/µL CM

Aim: check if wildtype has a resistance against CM

Result: Bacillus subtilis Wildtype 3610 did not grow on the 25 ng/µLCM plate

In order to check at which concentration CM Bacillus cannot survive he was plated out from an LB plate on LB-CM plates with different CM concentrations (5, 10, 15 ng/mL).

Incubation at 30°C over night.

10.06.2014

18.17 Checking Transformation of ligation from 18.16

Plate	Amount of colonies
Negative control	1
Ligation attempt 1	2
Ligation attempt 2	>80

18.18 Checking success of ligation via cPCR

Aim: A cPCR with the primers 54 and 56 shows the success of ligation by amplification of the Hag-construct.

In order to check the positive insertion of the DARPin gene into pMAD a PCR amplification with primers 54 and 56 for the flagellin should generate an ca. 1500 bp fragment on the gel. Negative clones would show still just a 1000 bp band because of the amplification of the Hag-Spe1 site construct. The picked clones were transferred on a new LB-amp plate. 12 clones were picked.

Mix	Master-Mix for 14 attempts (µL)	Mix for PCR attempt (µL)
Colony	-	part of a colony
Primer Flo 54	7	-
Primer Flo 56	7	-
Phusion	14	-
Phusion Buffer 5x	56	-
dNTP Mix	7	-
Water	189	-
Mastermix	-	20
Total Volume	280	20

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	1min 45sec
4	72	1 min
5	Go To 2	30x
6	72	4min
7	8	infinite

Expected bands:
Hag-DARPin-construct: ca. 1500 bp

Clone 1, 2, 3, 4, 5, 7, 9, 11 and 12 were the positive clones at 1500 bp.

18.19 Miniprep of positive clones

Aim: In order to check the orientation of the positive clones minipreps were inoculated for further experiments

Because of the ligation via 2 Spe1 sites the chance is 50:50 that the clones contain the pMAD-Hag-Flank-DARPin construct in the right orientation (Startcodon on the Hag1-site). For test digests the plasmids have to be amplified by minipreps.

The clones were used to inoculate 7 mL LB-Amp and incubated at 37°C Overnight.

13.64 checking Bacillus WT 3610 growth on 25 & 35 µg/µL CM

Aim: check if wildtype has a resistance against CM

Result: Bacillus subtilis Wildtype 3610 grew on the 5, 10 & 15µg//µl LB-CM plate.

We saw that Bacillus grew on almost every CM concentration except 25 µg/µL. So we transformed competent WT3610 with Nose plasmid piGEM-003 as a positive control and plated them out on LB-CM with 25 µg/µL and 35 µg/µL from Daniel Schindler.

Additionally WT from Felix Dempwolff which was made competent was also transformed with piGEM-004 was plated out on LB-CM with 5, 10 and 15 µg/mL CM to check if these cells can be selected better.

Incubation at 30°C for 2 days.

12.06.2014

18.19 Miniprep of positive clones

The concentration of the prepped plasmids was between 100 and 150 ng/µL.

18.20 Test digest with EcoRV

Aim: Checking the right orientation of the prepped plasmids

The plasmids from the positive clones were digested with EcoRV so that specific fragments emerge when cutting into the DARPin gene and the vector backbone.

Component	Volume [µl]	Mastermix for 10 attempts [µl]
Plasmid of clone	2 (ca. 200ng)	-
Cutsmart 10x	-	8
EcoRV	-	1
Milipore water	-	71
Mastermix	8	-
Total Volume	10	80

Right orientation: 7900 – 1570 – 2500 – 55
Wrong orientation: 7900 – 1170 – 2500 – 460

Clone 1, 2, 3, 4, 7, 9 and 11 have the right orientation.

12.06.2014

18.21 PCR with pMAD-Hag-Flank-DARPin (piGEM-019) and piGEM-005

Aim: Amplification of Hag-Spe1-construct and Hag-DARPin construct with Nco1/BamH1 sites for cloning into pet24d → crystallization of domains.

The templates (piGEM-005, prepped pasmid from clone 7 & 12 ) were diluted 1:10. piGEM-005 should function as a negative control. Clone 12 was picked in case the second orientation could be used for different experiments. 5 µL PCR product + 1 µL loading dye were analysed on an 1% agarose gel.

Mix	Volume
Template 1:10	1
Primer Flo 54	1
Primer Flo 56	1
Phusion	1
Phusion Buffer 5x	10
dNTP Mix	1
Water	35
Total Volume	50

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	1min 45sec
4	72	2 min
5	Go To 2	30x
6	72	4min
7	8	infinite

Expected bands:
clone 7 & 12 PCR product at ca. 1500bp – piGEM-005 PCR product at 1kb

18.22 restriction digest of Hag PCR fragments from 18.21 with Nco1/ BamH1

Aim: creating restriction sites for cloning into pet24d cut with Nco/Bam

The PCR products from 18.21 were digested with Nco1 and BamH1 to create restriction sites in order to ligate the fragments into Nco/Bam cut pet24d.

Component	Volume [µl]
PCR products	45
Cutsmart 10x	5,2
Nco1	1
BamH1	1
Water	2,8
Total Volume	52

Incubation for 2h at 37°C with heat shock at 80°C.

18.23 Ligation of pet24d and Hag PCR fragments from 18.22 cut with Nco/Bam

Aim: cloning inserts into pet24d for crystallization

The Nco/cut Flagellin PCR products from 18.22 (from clone 7 and piGEM-005) were ligated with Nco1 and BamH1 cut pet24d.

Component	Pet-Hag attempt (µL)	Pet-Hag-DARPin attempt (µL)
Insert (PCR fragments , c= ca. 400 ng/µL)	2	2
Vector (pet24d, c= 50ng/µL)	5	5
Ligase-Buffer 10x	2	2
T4 Ligase	1	1
Milipore Water	10	10
Total Volume	20	20

Incubation overnight at room temperature.

20.2 Transformation of competent Bacillus subtilis

Aim: transformation of plasmid into Bacillus subtilis WT3610

100 µL of overnight culture were added to 10 mL of MNGE-Medium and incubated till an OD of 1,1-1,3 at 37°C which could take 4-5h.

After reaching OD of 1,1-1,3 2 x 400 µL of the culture were transformed with 1,5 µg piGEM-005 and -018. After 1h incubation at 37°C 100 µL Expression mix were added and incubated for 1h as well.

In the end the 500 µL attempt was plated out on MLS-X-Gal plates and incubated at 30 °C overnight until colonies could be seen.

13.06.2014

18.24 Transformation of overnight ligation

Aim: checking success of ligation and amplification of ligated construct

The whole 20µL attempt was transformed into E.Coli X1-Blue, plated out on LB-Can plates and incubated at 37°C overnight.

18.25 Miniprep of pMAD-Hag-Flank-DARPin (piGEM-018)

Aim: Amplification of plasmids for work and storage

2x 6 mL of LB-Amp were inoculated with a colony from apiGEM-018 transformation plate and incubated at 37°C overnight.

18.26 sequencing of constructs

Aim: checking the right insertion into the plasmids

pMAD-Hag-Flank-DARPin and the hormone receptor clone 1 were given away in form of a premix with primers for sequencing. 10 µL with 50-100 ng/µL were mixed with 2 µL of primers for sequencing according to the following scheme:

Premix	Label-Nr.	Construct	Primer
1	391	pMAD-Hag-Flank-DARPin	Flo54 (Hag-F-Nco)
2	392	pMAD-Hag-Flank-DARPin	Flo56 (Hag-R-Bam)
3	393	pRSGII426+receptor gene	TW248
4	394	pRSGII426+receptor gene	TW249

13.65 checking Bacillus WT from Felix Dempwolff growth

Aim: check which WT can used for selection with Nose plasmids

Competent WT from Felix Dempwolff was transformed with piGEM-002, -003 and -004 by incubating the aliquods with 5 µL plasmid for 30 min at 37°C. After half an hour the whole attempt was plated out on LB-Cm (5 ng/µL).

Incubation at 30°C for 2 days.

14.06.2014

18.27 miniprep of inoculated plasmids from 18.25

Aim: isolation of plasmids

The miniprep of pMAD-Hag-Flank-DARPin was done according to the protocol of the OMEGA DNA kit.

18.28 pet24d digest with Nco/Bam

Aim: preparing vector for new ligation attempts

Because of the unsuccessful ligation from 18.23 new vector (pet24d) was cut with Nco1 and BamH1 according to the following scheme:

Component	Volume [µl]
Pet24d (148 ng/µL)	15
Cutsmart 10x	3
Nco1	0,5
BamH1	0,5
Water	6
Total Volume	30

Incubation at 37°C for 2h.

18.29 Pst1 digest of PCR fragments from piGEM-018 with Hag-primers

Aim: checking if the correct inserts are used for ligation

The DARPin-Hag constructs contain a Pst1 restriction site which could be used to check if the DARPin gene was inserted into the Hag-construct correctly again. For that purpose PCR products based on piGEM-018 from clone 7 and 12 (right and wrong orientation) as a template were cut with Pst1.

PCR products from clone 7: 658 bp and 781 bp fragment.

PCR products from clone 12:1000bp and 429 bp fragments.

Component	Volume [µl]
PCR fragment (350 ng/µL)	3
Cutsmart 10x	1
Pst1	0,5
Water	5,5
Total Volume	10

Incubation at 37°C for 2h.

18.30 PCR amplification of DARPin-Hag and Hag fragment

Aim: amplification of DARPin-Hag fragments for repeating the ligation

piGEM-018 & -005 were used as template for a PCR with the primers from Florian Altegoer 54 and 56. The products could be used for further cloning after Nco/Bam digest.

Mix	Volume
Template (piGEM-005 & -018)	1
Primer Flo 54	1
Primer Flo 56	1
Phusion	1
Phusion Buffer 5x	10
dNTP Mix	1
Water	35
Total Volume	50

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	1min 45sec
4	72	2 min
5	Go To 2	30x
6	72	4min
7	8	infinite

The fragments were analysed on an 1% agarose gel.

15.54 new PCR amplification of cup1-1

Aim: amplification of cup1-1 domain for Gibson assembly into pMAD

The cup1-1 domain was amplified via PCR with new primers iGEM-024 and -025. The fragment should be ca. 160 bp.

Mix	Volume
Template (cup1-1 gene)	1
Primer iGEM-024	1
Primer iGEM-025	1
Phusion	1
Phusion Buffer 5x	10
dNTP Mix	1
Water	35
Total Volume	50

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	30 sec
4	72	30 sec
5	Go To 2	30x
6	72	4min
7	8	infinite

Referring to the gel analysis the amplification was successful.

15.06.2014

20.3 Overnight culture of blue clones

Aim: transformation of plasmid into Bacillus subtilis WT3610

Colonies were grown on the plates with transformed piGEM-005 & - 018. The blue/ white screening showed positive transformed blue clones. 3 clones of different morphology per plate were picked and used for inoculation of LB-MLS (4 mL LB, 4 µL Lincomycin, 4 µL Erythromycin). Incubation was carried out overnight at 30°C with the 6 cultures.

17.06.2014

20.3 First temperature shift

Aim: integration of pMAD-Insert into Bacillus chromosome via flanks

The 6 overnight cultures were used to inoculate 10 mL LB MLS until the culture obtained an OD of 0,1. The cultures were incubated at 30°C for 2h.

Then the temperature was shifted to 42°C for 6h.

After the heat shock dilutions from 10-4 to 10-6 of each culture were plated out on MLS-X-Gal so that 18 plates could be incubated overnight at 42°C.

15.54 Gibson-assebmly with PCR amplificated cup1-1 and spe1 cut piGEM-005

Aim: insertion of cup1-1 into piGEM-005

The cup1-1 domain was amplified via PCR with new primers iGEM-024 and -025. Vector and template were diluted to a concentration under 75 ng/µL. Spe1 cut piGEM-005 was used from the cloning experiments with DARPin.

PCR fragment cup1-1 (464 ng/µL) dilution 1:10

Spe1 cut pIGEM-005 (148 ng/µL) dilution 1:2

Component	Volume [µl]
Gibson-Mix	15
Insert (cup1-1 58 ng/µL)	1,3
piGEM-005	1
Water	2,7
Total Volume	20

The mix was incubated 5 min at room temperature and then for 1h at 50°C.

In the end the whole mix was transformed into E.Coli XL1-Blue and plated out on LB-Amp. Incubation was done overnight at 37°C.

18.06.2014

20.4 Second temperature shift

Aim: flip out of the pMAD backbone

One blue colony per diluted clone was used to inoculate 4 mL LB. The 6 cultures were incubated at 30°C for 6h and afterwards for 3h at 42°C.

Dilutions from 10-4 to 10-6 were plated out on 18 X-Gal plates WITHOUT MLS selection. The positive clones should not contain the resistance inside the backbone as well as the galactosidase. The plates were incubated at 42°C overnight.

15.54 Checking Gibson assembly plate piGEM-005-cup1-1

Aim: insertion of cup1-1 into piGEM-005

Unfortunately the plate was empty, no colonies. The vector was cut newly in order to repeat the assembly.

15.55 restriction digest of piGEM-005 with spe1

Aim: linearizing plasmid for repeating the Gibson assembly

In order to repeat the Gibson assembly the piGEM-005 was cut with spe1 freshly.

Component	Volume [µl]
piGEM-005 (108 ng/µL)	10
Cutsmart 10x	2
Spe1	0,5
Water	7,5
Total Volume	20

Incubation 1h at 37°C with following heat shock at 80°C

19.06.2014

20.5 selection of positive clones

Aim: checking the correct flip out of the pMAD backbone

From the dilution plates was one WHITE clone picked and transferred on a Master X-Gal Plate as well as on a MLS plate so that 18 clones were proven for the right integration of the insert although flipping out the pMAD backbone.

The plates were incubated at 42°C overnight.

15.56 new Gibson-assembly with cup1-1 and spe1 cut piGEM-005

Aim: insertion of cup1-1 into piGEM-005

As insert cup1-1 PCR product from 15.55 and Spe1 cut piGEM-005 from 15.55 were used for a new Gibson assembly.

PCR fragment cup1-1 (464 ng/µL)

Spe1 cut pIGEM-005 (53 ng/µL)

Component	Volume [µl]
Gibson-Mix	15
Insert (cup1-1 58 ng/µL)	2,5
piGEM-005	2,5
Total Volume	20

The mix was incubated 5 min at room temperature and then for 1h at 50°C.

In the end the whole mix was transformed into E.Coli XL1-Blue and plated out on LB-Amp. Incubation was done overnight at 37°C.

20.06.2014

20.5 selection of positive clones

Aim: checking the correct flip out of the pMAD backbone

The white colonies grew on the X-Gal Master plates but not on MLS plates so the transformation seemed to be successful. The Backbone with the MLS resistance flipped out of the genome

20. 6 cPCR with checked clones

Aim: checking integration of constructs Hag-Spe and Hag-Spe-DARPin into B. s. genome

No clone was growing on MLS plates so the picked clones seemed to be positive. In order to check the correct integration of the domain constructs a cPCR with the picked clones on the X-Gal plates was done. The picked 18 B.s. clones were cooked in 10 µL PBS for 5 min at 95°C.

Mix	Master-Mix for 18 attempts (µL)	Mix for PCR attempt (µL)
Colony (picked clones 1-9 from Flagellin/-DARPin B.s. plates)	-	Part of a cooked colony
Primer Flo54 Hag-fw	9	-
Primer Flo56 Hag-rv	9	-
Phusion	18	-
Phusion Buffer 5x	72	-
dNTP Mix	9	-
Water	237	-
DMSO	6	-
Mastermix	-	20
Total Volume	100	360

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	1 min 45 sec
4	72	2 min
5	Go To 2	30x
6	72	4min
7	8	infinite

The gel showed no bands. The PCR had to be repeated.

15.57 Miniprep of clones from Gibson assembly from 15.56

Aim: Plasmid amplification for further experiments

4x 5 mL of LB-Amp was were inoculated with a picked colony from a transformation plate with XL1-Blue containing the Gibson-Assembly product from 15.56.

Incubation at 37°C overnight.

21.06.2014

15.58 cPCR with colonies from Gibson piGEM-005 + cup1-1 plate

Aim: checking correct insertion of cup1-1

In order to check the correct insertion of the cup1-1 domain into the Hag-Flank-construct in pMAD a cPCR with primers iGEM-025 (Cup1-1 rv) and Flo89 (pMAD-flank1-Bamh1 fw) was performed. The picked colonies were the same which wre used to inoculate minipreps from 15.57. The fragment was supposed to e ca. 1250 bp.

Mix	Master-Mix for 5 attempts (µL)	Mix for PCR attempt (µL)
Colony (picked clones 1-4 for miniprep)	-	Part of a colony
Primer Flo89	2,5	-
Primer piGEM-025	2,5	-
Phusion	2,5	-
Phusion Buffer 5x	20	-
dNTP Mix	2,5	-
Water	70	-
Mastermix	-	20
Total Volume	100	20

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	30 sec
4	72	1 min 30 sec
5	Go To 2	30x
6	72	4min
7	8	infinite

The analysis via 1% agarose gel eletrophoresis showed now bands. All 4 picked clones were prepped to use the plasmid as template.

15.59 PCR with prepped plasmid from Gibson piGEM-005 + cup1-1 plate

Aim: checking correct insertion of cup1-1

This time the prepped plasmid DNA from the picked 6clones was used as a template with different primer pairs. First of all tie PCR attempts were performed with primers Flo89 and Flo90 in order to receive the whole Hag-Flank-Cup1-1 construct with ca. 2100 bp length. As negative control also piGEM-005 was used as template producing a 2000kb fragment. Because of the small difference all 6 attempts were also driven with the primers Flo89 and iGEM-025 (cup1-1 rv) in order to check the insertion of cup1-1 directly with a fragment of 1268 bp.

Mix	Master-Mix 1 for 5 attempts (µL)	Master-Mix 2 for 5 attempts (µL)	Mix 1 for PCR attempt (µL)	Mix 2for PCR attempt (µL)
Plasmid DNA from clone 1-4/ piGEM-005	-	-	1	-
Primer Flo89	2,5	2,5	-	-
Primer Flo90	2,5	-	-	-
Primer piGEM-025	-	2,5	-	-
Phusion	2,5	2,5	-	-
Phusion Buffer 5x	20	20	-	-
dNTP-mix	2,5	2,5	-	-
Water	70	70	-	-
Master-Mix 1/ 2	-	-	20	20
Total Volume	100	100	20	20

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	30 sec
4	72	20 sec
5	Go To 2	30x
6	72	4min
7	8	infinite

The gel analysis shows that all 4 clones seem to be positive. By amplification of the cup1-1 fragment with the plasmid DNA as template could proof that.

20. 6 repeating cPCR with checked clones

Aim: checking integration of constructs Hag-Spe and Hag-Spe-DARPin into B. s. genome

Because of the unsuccessful cPCR before the PCR was repeated. The picked 18 B.s. clones were cooked in 30 µL PBS for 10 min at 95°C.

Mix	Master-Mix for 18 attempts (µL)	Mix for PCR attempt (µL)
Colony (picked clones 1-9 from Flagellin/-DARPin B.s. plates)	-	Part of a cooked colony
Primer Flo54 Hag-fw	9	-
Primer Flo56 Hag-rv	9	-
Phusion	18	-
Phusion Buffer 5x	72	-
dNTP Mix	9	-
Water	237	-
DMSO	6	-
Mastermix	-	20
Total Volume	100	360

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	1 min 45 sec
4	72	2 min
5	Go To 2	30x
6	72	4min
7	8	infinite

20. 6 repeating cPCR with checked clones

The clones with piGEM-005 seem to be positive all 9. Clone 1, 3, 7, 8 and 9 of transformed piGEM-018.1 might be positive as well as clone 2-6 from piGEM-018.2. The sequencing of the PCR products should tell us if the insertion was successful.

22.06.2014

18.31 PCR amplification of DARPin-Hag and Hag fragment

Aim: amplification of DARPin-Hag fragments for repeating the ligation

piGEM-018 & -005 were used as template for a PCR with the primers from Florian Altegoer 54 and 56. The products could be used for further cloning after Nco/Bam digest.

Content	Volume [µl]
Template (piGEM-005 & -018)	1
Primer Flo 54	1
Primer Flo 56	1
Phusion	1
Phusion Buffer 5x	10
dNTP Mix	1
Water	35
Total Volume	50

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	30 sec
4	72	1 min 45 sec
5	Go To 2	30x
6	72	4min
7	8	infinite

18.32 cPCR with new clones

Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pet24d

more clones from each plate were picked to analyse them via cPCR with the primers flo54 and flo56 (Hag-fw and Hag-rv). The result should be a ca. 1kb fragment for correct pet24d-Hag containing clones and a 1,5 kb fragment for pet24d-Hag-DARPin containing clones.

Content	Volume (µL)	MM for 14 attempts (µL
Colony (8-15 from pet-Hag,7-14 from pet-Hag-DARPin)	1 colony	-
Primer Flo 54	-	7
Primer Flo 56	-	7
Phusion	-	7
Phusion Buffer 5x	-	56
dNTP Mix	-	7
Water	-	196
Mastermix	20	-
Total Volume	20	280

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	30 sec
4	72	1 min 45 sec
5	Go To 2	30x
6	72	4min
7	8	infinite

18.33 pet24d digest with Nco/Bam

Aim: preparing vector for new ligation attempts

Because of the low amount of right clones new vector (pet24d) was cut with Nco1 and BamH1 according to the following scheme:

Component	Volume (µL)
Pet24d (50 ng/µL)	20
Cutsmart 10x	3
Nco1	0,5
BamH1	0,5
Water	6
Total Volume	30

Incubation at 37°C for 2h with heat shock in the end at 80°C

Endconcentration: 32 ng/µL

18.34 restriction digest of Hag PCR fragments from 18.31 with Nco1/ BamH1

Aim: creating restriction sites for cloning into pet24d cut with Nco/Bam

The PCR products from 18.x were digested with Nco1 and BamH1 to create restriction sites in order to ligate the fragments into Nco/Bam cut pet24d in case of negative clones refering to the cPCR from 18.x

Component	PCR Hag-fragment (µL)	PCR Hag-DARPin fragment (µL)
PCR products	45	45
Cutsmart 10x	5,2	5,2
Nco1	0,5	0,5
BamH1	0,5	0,5
Water	3,8	3,8
Total Volume	52	52

Incubation for 2h at 37°C with heat shock at 80°C.

Endconcentration:
digested Hag-fragment 260 ng/µL
digested Hag-fragment 268 ng/µL

15.60 PCR pMAD-Hag-Flank-cup1-1 (piGEM-016)

Aim: checking success of Gibson assembly with pMAD-Hag-Flank and cup1-1

Using the plasmids as template the cup1-1 fragment at 160 bp should be visible on the agarose gel. As positive control PCR products from the cup1-1 amplification used for the Gibson Assembly into piGEM-005 were applicated on the gel as well.

Content	Volume (µL)	MM for 5 attempts (µL)
Template (Plasmid from clone 1-4)	0,5	-
Primer iGEM-024	-	2,5
Primer iGEM-025	-	2,5
Phusion	-	2,5
Phusion Buffer 5x	-	20
dNTP Mix	-	2,5
Water	-	70
Mastermix	19,5	-
Total Volume	20	100

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	30 sec
4	72	20 sec
5	Go To 2	30x
6	72	4min
7	8	infinite

The bands under the 200 bp mark indicate the positive insertion of cup1-1 into piGEM-005. The plasmid has to be sequenced and is named iGEM-016.

18.35 test digest with Nco/Bam – Checking insertion of Hag/-DARPin into pet24d

Aim: proving insertion of Hag/-DARPin fragment into pet24d

The plasmids are digested with Nco1 and BamH1. In case of a correct insertion the pet24d backbone and the insert should be seen on the gel at 5300 bp and 1000/ 1500 bp. As control Pet24d-Hag-Flank (piGEM-001) is used to check the mastermix.

Component	Volume (µl)	Mastermix
2x Plasmid from clone 6	5	-
Cutsmart 10x	-	5
Nco1	-	0,5
BamH1	-	0,5
Water	-	19
Total Volume	10	25

18.36 ligation of pet24d and PCR Hag/ Hag-DARPin fragments cut Nco/Bam

Aim: ligation of construct with pet24d for overproduction of flagellin and crystallization

The Nco/cut Flagellin PCR products from 18.x (from clone 7 and piGEM-005) were ligated with Nco1 and BamH1 cut pet24d.

Component	Pet-Hag attempt (µL)	Pet-Hag-DARPin attempt (µL)
Insert (PCR fragments) (ca. 260 ng/µL)	2	2
Vector (pet24d, c= 50ng/µL)	5	5
Ligase-Buffer 10x	2	2
T4 Ligase	1	10
Milipore Water	10	10
Total Volume	20	20

The attempts were carried out in double and incubated at room temperature -One attempt for 1h followed by transformation into E.Coli XL1-Blue and the second one overnight.

18.37 repetition of PCR with 3 clones of Pet-Hag and Pet-Hag-DARPin ligation

Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pet24d

3 clones from ligation plates with pet-Hag and pet-Hag-DARPin were resuspended in 30 µL PBS and cooked at 95 °C for 10min. After that procedure 1 µL of this suspenion was used as PCR template.

Content	Volume (µL)	MM for 7 attempts (µL)
Template ( 1µL cooked suspension) (8-10 from pet-Hag, 7-9 from pet-Hag-DARPin)	1	-
Primer Flo 54	-	3,5
Primer Flo 56	-	3,5
Phusion	-	3,5
Phusion Buffer 5x	-	28
dNTP-mix	-	3,5
Water	-	98
Mastermix	19	-
Total Volume	20	140

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	30 sec
4	72	1 min 45 sec
5	Go To 2	30x
6	72	4min
7	8	infinite

Run overnight

Transformation

Plasmid	Concentration (ng/µL)	Antibiotic	Cells	Volume (µL)
Pet24d	148	Can	DH5α	1
piGEM-018	160	Amp	DH5α	0,5
piGEM-014	350	Amp	DH5α	0,5
Gibson pMAD-cup1-1 clone 4	60	Amp	DH5α	1
Pet-Hag attempt from 18.36	-	Can	XL1-Blue	20
Pet-Hag-DARPin attempt from 18.36	-	Can	XL1-Blue	20
Control pet24d cut Nco/Bam	32	Can	XL1-Blue	1

23.06.2014

Sequencing of constructs from 23.06.2014

Premix	Label-Nr.	Construct	Primer
1	AGB0023402	piGEM-018 (pMAD-DARPin)	Flo54 (Hag-F-Nco)
2	AGB0023403	piGEM-018 (pMAD-DARPin)	Flo56 (Hag-R-Bam)
3	AGB0023404	pMAD-Hag-Flank-cup1-1	Flo54 (Hag-F-Nco)
4	AGB0023405	pMAD-Hag-Flank-cup1-1	Flo56 (Hag-R-Bam)
5	AGB0023406	piGEM-002 (Nose plasmid)	TW259

18.37 repetition of PCR with 3 clones of Pet-Hag and Pet-Hag-DARPin ligation

Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pet24d

Gel electrophoresis:

The gel shows negative bands in case of the Hag-DARPin clones. The PCR for Hag 8 and 9 did not work although we cooked the clones with PBS. The transformation efficiency seemed to be very low so clones from the new ligation attempts should be analysed.

18.38 ligation checking success of transformed ligation attempts

On every plate grew a high amount of colonies. 6 clones of each plate were picked for inoculation of minipreps and for cPCR after cooking with PBS. The clones were transferred to another LB-Can plate.

18.39 cPCR with picked clones from 18.38 ligation attempt transformation

Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pet24d

For checking the insertion of the Hag/-DARPin into pet24 the clones from the transformation plate were transferred to another LB-Can plate and cooked for 10 min in 30µL PBS at 95°C. At the same time the colonies were used to inoculate LB-Can for minipreps.

Content	Volume (µL)	MM for 14 attempts (µL)
Template ( 1µL cooked suspension) (1-6 from pet-Hag, 1-6 from pet-Hag-DARPin)	1	-
Primer Flo 54	-	7
Primer Flo 56	-	7
Phusion	-	7
Phusion Buffer 5x	-	198
dNTP-mix	-	7
Water	-	98
Mastermix	19	-
Total Volume	20	280

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	30 sec
4	72	1 min 45 sec
5	Go To 2	30x
6	72	4min
7	8	infinite

Run overnight

25.06.2014

Sequencing results of constructs from 23.06.2014

Premix	Label-Nr.	Construct	Result
1	AGB0023402	piGEM-018 (pMAD-DARPin)	Correct insertion of DARPin
2	AGB0023403	piGEM-018 (pMAD-DARPin)	Did not work
3	AGB0023404	pMAD-Hag-Flank-cup1-1	Correct insertion, point mutation refers to bad sequencing
4	AGB0023405	pMAD-Hag-Flank-cup1-1	Did not work
5	AGB0023406	piGEM-002 (Nose plasmid)	Correct insertion of the CM resistance

18.39 Gel cPCR with picked clones from 18.38 ligation attempt transformation

Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pet24d

Gel electrophoresis: no bands except for the controls were seen. The PCR has to be repeated with more colony in the PCR tubes or the prepped plasmids

18.40 test digest with Nco/Bam of prepped plasmids from picked colonies

Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pet24d

The picked clones from the ligation attempts 18.38 were prepped. In order to check the insertion of the Hag/ Hag-DARPin domain the plasmids were digested with Nco1/ BamH1 so that the gel should show the insert of 1 or 1,5 bp length and the pet24d backbone at 5300 bp. Because of an unavailable marker as a control the PCR amplified inserts which were used for the ligation will run with the gel as well. piGEM-001 will also be cut Nco/Bam in order to receive a marker band for the pet24d backbone.

Component	Volume (µL)	Mastermix for 8 attempts
Plasmid (ca. 45 ng/µL	5	-
Cutsmart 10x	-	4
NcoI	-	0,5
BamH1	-	0,5
Water	-	35
Mastermix	5	-
Total Volume	10	40

20.6 Purification of cPCR samples with Gel extraction kit

Aim: purification of samples for sequencing

Purified samples:
clone 3 & 5 from transformed piGEM-005
clone 3 & 9 from transformed piGEM-018

Clone	Concentration (ng/µl)
Hag 3	10
Hag 5	14
Hag-DARPin 3	9
Hag-DARPin 9	9

26.06.2014

20.7 PCR with purified cPCR samples from 20.x

Aim: PCR amplification of purified cPCR samples

The concentration of the cPCR samples after purification was too low for sequencing. Therefore the cPCR samples have to be amplified with PCR again.

Content	Volume (µL)	MM for 6 attempts (µL)
Purified cPCR product from 20.x (3 & 5 from pet-Hag, 3 & 9 from pet-Hag-DARPin)	1	-
Primer Flo 54	-	6
Primer Flo 56	-	6
Phusion	-	6
Phusion Buffer 5x	-	6
dNTP-mix	-	60
Water	-	216
Mastermix	19	-
Total Volume	20	300

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	30 sec
4	72	1 min 45 sec
5	Go To 2	30x
6	72	4min
7	8	infinite

20.8 Sequencing of purified cPCR samples from pMAD transformation

Premix	Label-Nr.	Construct	Primer
1	AGB0023407	Hag-Spe1 in B.s. genome clone 3	Hag-Nco-fw
2	AGB0023408	Hag-Spe1 in B.s. genome clone 5	Hag-Nco-fw
3	AGB0023409	Hag-Spe1-DARPin in B.s. genome clone 3	Hag-Nco-fw
4	AGB0023410	Hag-Spe1-DARPin in B.s. genome clone 9	Hag-Nco-fw

18.41 new ligation of pet24d and PCR Hag/ Hag-DARPin fragments cut Nco/Bam transformation

Aim: ligation of construct with pet24d for overproduction of flagellin and crystallization

The cut pet24d Nco/Bam which was used for the previous ligations was not purified and contained an 1 kb insert. For a new cealn ligation the attempt was repreated with pet24d cut by Carina Knauer .The Nco/cut Flagellin PCR products (from clone 7 and piGEM-005) were ligated with Nco1 and BamH1 cut pet24d.

The attempts were carried out in double. The attempts 1 & 2 were incubated 1h at room temperature and finally transformed into E. Coli XL1-Blue after inactivation at 65 for 10 min. The attempts 1.1 and 2.1 were incubated overnight at room temperature. 1 µL of cut vector was transformed as a negative control in order to check the amount of religants.

Component	Pet-Hag attempt (µL) – 1 & 1.1	Pet-Hag-DARPin attempt (µL) 2& 2.1
Insert (PCR fragments) (ca. 260 ng/µL)	3	3
Vector (pet24d, c= 86ng/µL)	5	5
Ligase-Buffer 10x	2	2
T4 Ligase	1	1
Millipore water	9	9
Total Volume	20	20

27.06.2014

18.42 Miniprep of ligation clones

The ligation between pet24d and the Hag-/Hag-DARPin fragments which were both cut Nco/Bam was successful. The ligation plates showed over 20 clones each whereby on the negative control grew a few clones as well which were very small and sticking together. Bad plate out might be the reason for that. In order to analyse the insert of the clones 5 clones per ligation plate 1 and 2 were used to inoculate minipreps in 5 mL LB-Can. For the Ligation 1 Pet-Hag clones 1-5 were picked, as well as clones 6-10 from Plate Ligation 2 Pet-Hag-DARPin.

The cultures were inoculated overnight at 37°C.

28.06.2014

18.42 Miniprep of ligation clones

Construct	Clone	Concentration (ng/µL)
Pet-Hag	1	50
Pet-Hag	2	87
Pet-Hag	3	65
Pet-Hag-DARPin	6	83
Pet-Hag-DARPin	7	59

18.43 cPCR of clones from 18.42

Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pet24d

Plasmid from prepped clones from each plate were analysed via cPCR with the primers flo54 and flo56 (Hag-fw and Hag-rv). The result should be a ca. 1kb fragment for correct pet24d-Hag containing clones and a 1,5 kb fragment for pet24d-Hag-DARPin containing clones.

Content	Volume (µL)	MM for 6 attempts (µL)
Picked clones from 18.42 (1-3pet-Hag, 6-7 from pet-Hag-DARPin)	0,5	-
Primer Flo 54	-	3
Primer Flo 56	-	3
Phusion	-	3
Phusion Buffer 5x	-	6
dNTP-mix	-	24
Water	-	81
Mastermix	19,5	-
Total Volume	20	120

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	30 sec
4	72	1 min 45 sec
5	Go To 2	30x
6	72	4min
7	8	infinite

18.44 test digest with Nco/Bam – Checking insertion of Hag/-DARPin into pet24d

Aim: proving insertion of Hag/-DARPin fragment into pet24d

The plasmids were digested with Nco1 and BamH1. In case of a correct insertion the pet24d backbone and the insert should be seen on the gel at 5300 bp and 1000/ 1500 bp. As control Pet24d-Hag-Flank (piGEM-001) is used to check the mastermix.

Component	Volume (µL)	Mastermix(6 attempts)
Plasmid from clone ( Pet-Hag 1-3, Pet-Hag-DARPin 6 & 7)	5	-
Cutsmart 10x	-	3
NcoI	-	0,5
BamHI	-	0,5
Water	-	26
Total Volume	10	30

20.9 Gel Purification of amplified cPCR products

Aim: Purification for more efficient sequencing

The PCR product of the amplification of cPCR products was not pure considering different bands on the gel next to the right one. In order to exclude sequencing mistakes the PCR attempts were purified via gel extraction of the 1,5 kb band in case of the Hag-DARPin construct.

20.8 PCR with Gel Purified Hag-DARPin cPCR products for sequencing

Aim: amplification of purified Hag-DARPin fragment for sequencing

The purified cPCR product from 20.x has to be amplified again in order to get a higher concentration for sequencing.

Content	Volume (µL)	MM for 2 attempts (µL)
Purified PCR product from 20.x (Hag-/ Hag-DARPin fragment)	1-2	-
Primer Flo 54	-	1
Primer Flo 56	-	1
Phusion	-	1
Phusion Buffer 5x	-	2
dNTP-mix	-	20
Water	-	75
Mastermix	19	-
Total Volume	20	100

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	30 sec
4	72	1 min 45 sec
5	Go To 2	35x
6	72	4min
7	8	infinite

Transformation

Plasmid	Concentration (ng/µL)	Antibiotic	Cells	Volume (µL)
Pet-Hag clone 2	87	Can	DH5α	1
Pet-Hag clone 3	65	Can	DH5α	1
Pet-Hag-DARPin clone 7	59	Can	DH5α	1
Gibson Pet-Hag-Cup1-1	-	Can	DH5α	20

18.45 Spe1 digest of Pet-Hag (piGEM-019)

Aim: linearizing Pet24d-Hag with Spe1 site for a Gibson assembly with Cup1-1

Component	Volume (µL)
piGEM-016 (ng/µL)	17
Cutsmart 10x	2
Spe1	0,5
Water	0,5
Total Volume	20

Incubation 1h at 37°C with following heat shock at 80°C

18.46 Gibson assembly with linearized Pet-Hag (piGEM-019) and Cup1-1

Aim: Insertion of Cup1-1 domain into Pet-Hag construct for crystallization

As insert cup1-1 PCR product from 15.55 and Spe1 cut piGEM-016 from 18.44 were used for a new Gibson assembly.
PCR fragment cup1-1 (464 ng/µL)
Spe1 cut pIGEM-005 ( ng/µL)

Component	Volume (µl)
Gibson-mix	15
Insert (cup1-1 464 ng/µL)	2,5
piGEM-019	2,5
Total Volume	20

The mix was incubated 5 min at room temperature and then for 1h at 50°C.

In the end the whole mix was transformed into E.Coli XL1-Blue and plated out on LB-Amp. Incubation was done overnight at 37°C.

29.06.2014

18.47 cPCR of Gibson assembly lones of Pet-Hag (piGEM-019) and Cup1-1

Aim: screening clones for right insert

In order to screen the clones for the right insertion of cup1-1 4 clones were picked from the LB-Can plate and transferred to a LB-Can Master plate. Additionally the clones were used for inoculation of minipreps and also cooked in 50 µL dest. Water for 10 min at 95°C. The lysate was used as template.

The PCR with Flo54 and iGEM-025 should generate a 785 bp fragment and the one with iGEM-024 and -025 the 164bp domain fragment.

Content	Volume (µL)	MM 1 for 5 attempts (µL)	MM 2 for 5 attempts (µL)
Cooked lysate solution from clones 1-4	3	-
Primer Flo 54	-	2,5	-
Primer iGEM-024	-	-	2,5
Primer iGEM-025	-	-	2,5
dNTP-mix	-	2,5	2,5
Phusion	-	5	5
Phusion Buffer 5x	-	20	20
Water	-	67,5	67,5
Mastermix	17	-	-
Total Volume	20	100	100

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	30 sec
4	72	1 min 45 sec
5	Go To 2	35x
6	72	4min
7	8	infinite

The PCR showed no bands. The colonies were used for minipreps so that the isolated plasmid can the used for analysis of the insert.

30.06.2014

18.48 miniprep of clones from Gibson assembly with Pet-Hag (piGEM-019) and Cup1-1

Aim: isolation of Plasmid DNA for further experiments

Construct	Clone	Concentration (ng/µL)
Pet-Hag-Cup1-1	1	122
Pet-Hag-Cup1-1	2	85
Pet-Hag-Cup1-1	3	172
Pet-Hag-Cup1-1	4	116

Sequencing

Premix	Label-Nr.	Construct	Primers
1	AGB0023411	Pet24d-Hag-Spe1 construct cl. 2	Hag-Nco-fw
2	AGB0023412	Pet24d-Hag-DARPin construct cl. 7	Hag-Nco-fw

18.48 PCR of prepped Gibson assembly clones ( Pet-Hag (piGEM-019) and Cup1-1)

Aim: screening clones for right insert

The isolated plasmid 1:10 diluted from the picked clones 1-4 were used as PCR template.

The PCR with Flo54 and iGEM-025 should generate a 785 bp fragment and the one with iGEM-024 and -025 the 164bp domain fragment.

Content	Volume (µL)	MM 1 for 5 attempts (µL)	MM 2 for 5 attempts (µL)
Cooked lysate solution from clones 1-4 (1:10)	3	-
Primer Flo 54	-	2,5	-
Primer iGEM-024	-	-	2,5
Primer iGEM-025	-	2,5	2,5
dNTP-mix	-	2,5	2,5
Phusion	-	5	5
Phusion Buffer 5x	-	20	20
Water	-	67,5	67,5
Mastermix	17	-	-
Total Volume	20	100	100

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	30 sec
4	72	1 min 45 sec
5	Go To 2	35x
6	72	4min
7	8	infinite

No bands were shown on the gel. The PCR was repeated with Q5 mastermix to exclude the disfunction of the polymerase.

20.9 inoculation of preculture from Bacillus WT 3610

Aim:Preparation of for mainculture the next day

2x6 mL of LB were inoculated with Bacillus WT3610 from an LB plate and incubated at 37°C overnight.

@@ Line 5: / Line 5: @@
 {{Team:Marburg/Template:StartContinue}}
 {{Team:Marburg/Template:Submenu:Notebook:June}}
+<html>
-...
+<!-- 02.06.14 -->
+<div class="notebooky-entry">
+<h2 class="title">
+	<a name="02.06.14">02.06.2014</a>
+</h2>
+<fieldset class="exp13">
+    <legend><a name="exp13.56">13.56 Make Gly Stocks of the following strains </a></legend>
+	<div class="aim">
+		<p>Aim: Have gly stocks</p>
+    </div>
+    <div class="exp-contest">
+    	<ul class="list">
+        	<li>Dh5a pRSII426 –hGRa</li>
+            <li>Dh5a piGEM010 (p003 + Tag 21)</li>
+            <li>Dh5a piGEM015 (p004 + Tag 23)</li>
+            <li>Dh5a piGEM014 (p003 + Tag 22)</li>
+            <li>Dh5a piGEM008 (p002 + Tag 22)</li>
+            <li>Dh5a piGEM007 (p002 + Tag 21)</li>
+            <li>Dh5a piGEM011 (p003 + Tag 22)</li>
+            <li>Dh5a piGEM012 (p003 + Tag 23)</li>
+        </ul>
+    </div>
+</fieldset>
+<fieldset class="exp13">
+    <legend><a name="exp13.57">13.57 Mini Prep of  cultures inoculated on Friday 30.5. Nose Plasmids</a></legend>
+    <div class="exp-content">
+    	<ul class="list">
+        	<li>piGEM010 = 22ng/&micro;l</li>
+            <li>piGEM013 = 46 ng/&micro;l</li>
+            <li>piGEM 009 = 13 ng/&micro;l</li>
+        </ul>
+        <p>low concentration: new transformation to gain more plasmid DNA<br />
+		Strain: new competent <em>E. coli</em> XL1-blue</p>
+    </div>
+</fieldset>
+<fieldset class="exp15">
+    <legend><a name="exp15.50">15.50 Miniprep of pMAD-fla-cup1-1  for miniprep</a></legend>
+    <div class="exp-content">
+    <p>The miniprep was performed accoding to the miniprep protocol.</p>
+    <p>Concentration 40 ng/&micro;L<br />
+    low concentration: new transformation to gain more plasmid DNA should be done<br  />
+    Strain: new competent <em>E. coli</em> XL1-blue</p>
+    </div>
+</fieldset>
+<fieldset class="exp13">
+    <legend><a name="exp13.58">13.58 Bacillus Trafo with all Nose Plasmids containing one/no Degradation Tag</a></legend>
+    <div class="aim">
+    <p>Aim:  Create Bacillus subtilis strain 3610 containing the following plasmids: piGEM002 to 004 and piGEM007 to 016</p>
+    </div>
+    <div class="exp-content">
+    <p>Add 5&micro;l plasmid DNA and incubate for 30 min at 37&deg;C, LB plate with 5 ng/&micro;L Cm (prepared freshly)</p>
+    </div>
+</fieldset>
+<fieldset class="exp13">
+    <legend><a name="exp13.59">13.59 Inoculation of <em>Bacillus subtilis</em> wildtype (3610), gfp (186) and silver nose</a></legend>
+    	<div class="aim">
+        <p>Aim: Aim: MTA tomorrow to check out what concentrations of Ag+ are still okay for the cells to survive, since 1mM until 10&micro;M was too high and the cells died</p>
+        </div>
+        <div class="exp-content">
+        <p>Starting from 1 mM 8 dilutions have been prepared</p>
+        </div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.1">18.1 Tumor Terminator - Dilution of Plasmid</a></legend>
+    	<div class="aim">
+        <p>Aim: Creating a stock solution</p>
+        </div>
+        <div class="exp-content">
+       <img src="https://static.igem.org/mediawiki/2014/0/0e/MR_2014-06-02_plasmidmap.png" width="50%" />
+       <p>We received the synthetized DARPin-gene in a pEC-A2 vector with spe1 restriction sites at the 5’- and 3’-site at an amount of 2,7&micro;g plasmid in the tube.</p>
+       <p>A stock solution was created by adding 27&micro;l water to the tube.</p>
+       <p>Concentration of stock solution = 100 ng/&micro;l</p>
+       <p>A 1:10 dilution was created by using 1&micro;l of stock solution adding 9µL of water to an end concentration of 10ng/&micro;l.</p>
+       <p>Concentration of stock dilution = 10 ng/&micro;l.</p>
+        </div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.2">18.2 Transformation of DARPin-gene in plasmid into <em>E.Coli</em> XL1-Blue</a></legend>
+    	<div class="aim">
+        <p>Aim: Transforming pEX-A2 plasmid with DARPin-gene into E.Coli for amplification of the Gene.</p>
+        </div>
+        <div class="exp-content">
+       <p>1&micro;l of the 1:10 stock dilution were used for transformation of <em>E. Coli</em> XL1-Blue</p>
+        </div>
+</fieldset>
+</div>
+<!-- 03.06.14 -->
+<div class="notebooky-entry">
+<h2 class="title">
+	<a name="03.06.2014">03.06.2014</a>
+</h2>
+<fieldset class="exp18">
+    <legend><a name="exp18.3">18.3 Miniprep of DARPin-gene in plasmid in <em>E.Coli</em> XL1-Blue</a></legend>
+    <div class="aim">
+    <p>Aim: Receiving a higher amount of plasmid for further experiments.</p>
+    </div>
+    <div class="exp-content">
+    <p>3 x6ml LB-Amp were inoculated with clones from the successful transformed plate (18.2) and incubated at 37&deg;C overnight.</p>
+    </div>
+</fieldset>
+<fieldset class="exp13">
+    <legend><a name="exp13.60">13.60 Microtiter plate assay with wildtype, gfp strain 186 and silver nose</a></legend>
+    <div class="aim">
+    <p>Aim: MTA tomorrow to check out what concentrations of Ag+ are still okay for the cells to survive, since 1mM until 10 &micro;M was too high and the cells died</p>
+    </div>
+    <div class="exp-content">
+    <p>Starting from 1 mM 8 dilutions have been prepared.<br />In the beginning Minimalmedium S750 has been prepared with 0.5&permil; Xylose<br />In the wells the following mix was added to a total volume of 150 &micro;l:<br />135&micro;l of MM (90&permil;) and Silver solution (10&permil;)<br />15&micro;l of cells<br />Finally 70 &micro;l are added to avoid evaporation of the medium</p>
+    <p>Incubation for appr. 24h at 37&deg;C shaking (Viktor AG Waldminghaus)</p>
+    </div>
+</fieldset>
+<fieldset class="exp13">
+    <legend><a name="exp13.61">13.61 Checking Bacillus Trafo with all Nose Plasmids containing one/no Degradation Tag</a></legend>
+    <div class="exp-content">
+    <p>Every transformation plate showed a huge growth of bacillus without single colonies. After one day of incubation this seems to be an unrealistic growth which is why we plan to repeat the transformation after checking the growth of the <em>Bacillus subtilis</em> Wildtype 3610 on LB-CM plate with 5 &micro;g/ml CM.</p>
+    </div>
+</fieldset>
+<fieldset class="exp13">
+    <legend><a name="exp13.62a">13.62 Checking Bacillus Trafo Wildtype 3610</a></legend>
+    <div class="aim">
+    <p>Aim: check if wildtype has a resistance against CM or if the plates are not effective/ made wrong</p>
+    </div>
+    <div class="exp-content">
+    <p>Bacillus subtilis Wildtype 3610 was plated on LB-CM plate with 5 &micro;g/ml CM and incubated overnight at 37&deg;C.</p>
+    </div>
+</fieldset>
+<fieldset class="exp15">
+    <legend><a name="exp15.51">15.51 Making selection plates for clean deletions – integration of pMAD-construct into Bacillus subtilis chromosome</a></legend>
+    <div class="aim">
+    <p>Aim: For the integration of the constructs we cloned into pMAD many steps of a special selection are necessary.  For the protocoll we received from Florian Altegoer MLS and MLS X-gal plates have to be used.</p>
+    </div>
+    <div class="exp-content">
+    <p>Antibiotics and chemicals:</p>
+    <ul class="list">
+    <li>Erythromycin 4 mg/ml</li>
+    <li>Lincomycin 25mg/ml</li>
+    <li>X-Gal 100mg/ml</li>
+    </ul>
+    <p>For MLS selection plates Erythromycin with 1mg/ml were needed. Therefore the 4 mg/mL stock solution was diluted 1:4 by mixing 400 &micro;l Eryhtomycin with 1200 &micro;l of 70&deg; ethanol.</p>
+    <p>3 types of plates were made:</p>
+    <ul class="list">
+    <li>1.	MLS selectin: 800 mL LB agar + 800 &micro;l Eryhtromycin + 800 &micro;l Lincomycin</li>
+    <li>2.	MLS X-Gal: 800 mL LB agar + 800 &micro;l Eryhtromycin + 800 &micro;l Lincomycin + 800 &micro;l X-Gal</li>
+    <li>3. X-Gal: 800 mL LB agar + 800 µL X-Gal
+    </ul>
+    <p>About 120 plates were stored at the 4&deg;C room at AG Graumann labs.</p>
+    </div>
+</fieldset>
+</div>
+<!-- 04.06.14 -->
+<div class="notebooky-entry">
+<h2 class="title">
+	<a name="04.06.2014">04.06.2014</a>
+</h2>
+<fieldset class="exp18">
+    <legend><a name="exp18.4">18.4 Miniprep of DARPin-gene in plasmid in <em>E.Coli</em> XL1-Blue</a></legend>
+    <div class="exp-content">
+    <table width="100%" border="1">
+      <tr>
+        <th scope="col">Plasmid pEX-A2 + DARPinEc1</th>
+        <th scope="col">Concentration after prep (ng/&micro;l)</th>
+      </tr>
+      <tr>
+        <td>Clone 1</td>
+        <td>398,7</td>
+      </tr>
+      <tr>
+        <td>Clone 2</td>
+        <td>340</td>
+      </tr>
+      <tr>
+        <td>Clone 3</td>
+        <td>309</td>
+      </tr>
+</table>
+    </div>
+</fieldset>
+<fieldset class="exp15">
+    <legend><a name="exp15.52">15.52 Sequencing pMAD-fla-cup1-1</a></legend>
+    <div class="aim">
+    <p>Aim: Checking the correct insertion of the metallothionein-domain into the hag –flank construct</p>
+    </div>
+    <div class="exp-content">
+    <p>Making a pre-mix for Eurofins MWG prepairing the sequencing. Primers from Florian Altegoer were used:</p>
+    <ul class="list">
+    <li>Flo83- Hag11_fw 1:10 with 1&micro;l primer and 9&micro;l water</li>
+    <li>	Flo86- Hag12_rv 1:10 with 1&micro;l primer and 9&micro;l water</li>
+    </ul>
+    <table width="100%" border="1">
+      <tr>
+        <th scope="col">&nbsp;</th>
+        <th scope="col">Pre-mix 1 (&micro;L)</th>
+        <th scope="col">Pre-mix 2 (&micro;L)</th>
+      </tr>
+      <tr>
+        <th scope="row">piGEM-016 pMAD-cup1-1<br />40ng/&micro;L</th>
+        <td>10</td>
+        <td>10</td>
+      </tr>
+      <tr>
+        <th scope="row">Flo83- Hag11_fw</th>
+        <td>2</td>
+        <td>-</td>
+      </tr>
+      <tr>
+        <th scope="row">Flo86- Hag12_rv</th>
+        <td>-</td>
+        <td>2</td>
+      </tr>
+      <tr>
+        <th scope="row">Total Volume</th>
+        <td>12</td>
+        <td>12</td>
+      </tr>
+    </table>
+	<br />
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Label</th>
+    <th scope="col">Pre-mix 1</th>
+    <th scope="col">Primer</th>
+  </tr>
+  <tr>
+    <th scope="row">AGB0023375</th>
+    <td>Pre-mix 1</td>
+    <td>Flo83 &ndash; Hag11_fw</td>
+  </tr>
+  <tr>
+    <th scope="row">AGB0023374</th>
+    <td>Pre-mix 1</td>
+    <td>Flo86 - Hag12_rv</td>
+  </tr>
+	</table>
+    </div>
+</fieldset>
+<fieldset class="exp13">
+    <legend><a name="exp13.62b">13.62 Checking Bacillus Trafo Wildtype 3610</a></legend>
+    <div class="aim">
+    <p>Aim: check if wildtype has a resistance against CM or if the plates are not effective/ made wrong</p>
+    </div>
+    <div class="results">
+    <p>Result: Bacillus subtilis Wildtype 3610 grew on the CM plate which shows us that there has to be a mistake in making the LB-CM plates or the WT has a resistance.</p>
+    </div>
+    <div class="exp-content">
+    <p>In order to exclude the false making of plates new ones were made with new CM-stocks with 25 mg/ml and 5 mg/ml.</p>
+    <p>3 aliquots of competent <em>B.s.</em> WT3610 were plated on new LB-CM plates and incubated at 37&deg;C.</p>
+    </div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.5">18.5 Spe1 restriction of DARPin-gene in pEX-A2 & pMAD-hag-flank (piGEM-005)</a></legend>
+    <div class="aim">
+    <p>Aim: Receiving iGEM-005 as linearized vector for cloning the DARPin gene with Spe1 sites into pMAD-fla (iGEM-005) </p>
+    </div>
+    <div class="exp-content">
+    <table width="100%" border="1">
+      <tr>
+        <th scope="col">Restriction</th>
+        <th scope="col"><strong>pEX-A2-DARPin  digest (&micro;l)</strong></th>
+        <th scope="col"><strong>pMAD-Hag-Flank  digest (&micro;l</strong>)</th>
+        <th scope="col"><strong>Spe1-Mastermix</strong></th>
+      </tr>
+      <tr>
+        <th scope="row">pEX-A2+DARPin (398 &micro;g/&micro;L)</th>
+        <td>15 = ca. 6&micro;g</td>
+        <td>-</td>
+        <td>-</td>
+      </tr>
+      <tr>
+        <th scope="row">pMAD-Fla (114 &micro;g/&micro;L)</th>
+        <td>-</td>
+        <td>10= ca. 1,14 &micro;g</td>
+        <td>-</td>
+      </tr>
+      <tr>
+        <th scope="row"><em>Spe</em>I</th>
+        <td>-</td>
+        <td>-</td>
+        <td>1,5</td>
+      </tr>
+      <tr>
+        <th scope="row">CutSmart-Buffer (10x)</th>
+        <td>-</td>
+        <td>-</td>
+        <td>2</td>
+      </tr>
+      <tr>
+        <th scope="row">H2O</th>
+        <td>-</td>
+        <td>-</td>
+        <td>16,5</td>
+      </tr>
+      <tr>
+        <th scope="row">Mastermix</th>
+        <td>5</td>
+        <td>10</td>
+        <td>-</td>
+      </tr>
+      <tr>
+        <th scope="row">Total</th>
+        <td>20</td>
+        <td>20</td>
+        <td>20</td>
+      </tr>
+    </table>
+    <p>Incubation at 37&deg;C for 2h and heat shock at 81&deg;C for 5 min. After that the pMAD-Hag-Flank-Construct was purified with the OMEGA gel extraction kit according to the protocol.</p>
+    <p>c(digested piGEM-005)= 4 ng/&micro;l</p>
+    </div>
+</fieldset>
+<fieldset class="exp13">
+    <legend><a name="exp13.62c">13.62 Checking Bacillus Trafo Wildtype 3610</a></legend>
+    <div class="aim">
+    <p>Aim: check if wildtype has a resistance against CM or if the plates are not effective/ made wrong</p>
+    </div>
+    <div class="exp-content">
+    <p>Result: Bacillus subtilis Wildtype 3610 grew on the CM plate. We have already repeated making plates so it might be that the WT has got a resistance while making it competent. New WT from Florian Altegoer was plated on 2 CM plates with 5µg/µL (old and new one) and 2x LB plates from gly stocks.</p>
+    <p>Incubation at 37&deg;C overnight.</p>
+    </div>
+</fieldset>
+</div>
+<!-- 06.06.14 -->
+<div class="notebooky-entry">
+<h2 class="title">
+	<a name="06.06.2014">06.06.2014</a>
+</h2>
+<fieldset class="exp19">
+    <legend><a name="exp19">19. Crystallization of flagellin</a></legend>
+    <div class="concent">
+    <p>In order to cristallize flagellin with a domain it is necessary to produce the protein by E.Coli in a high concentration.  For that aim the Fla-construct will be amplificated out of pet24d which includes a domain. For elimination of the flanks a PCR has to be perfomed which just amplificates Hag with Domain and creates Nco1 and BamH1 restriction sites. After purification and digest with Nco/Bam the fragment can be ligated into Nco/Bam digested pet24d . After transformation the synthesis can be induced by IPTG.</p>
+    </div>
+</fieldset>
+<fieldset class="exp19">
+    <legend><a name="exp19.1">19.1 Eliminiation of flanks from Fla-construct including cup1-1out of pet24d</a></legend>
+    <div class="aim">
+    <p>Aim: Preparation for using pet24d as expression vector for flagellin</p>
+    </div>
+    <div class="exp-content">
+    <p>The flagellin construct was  amplificated with Primer 95 and 54 from Florian Altegoer which allow the  amplification of the construct with cup1-1 without flanks (just Hag) including  Nco1 &amp; BamH1 restriction sites.<br />
+      Template dilution 1:10:<br />
+&micro;L pet24d-cup1-1 was mixed with  9 &micro;L to an 1:10 dilution of 16,3 ng/&micro;L<br />
+      Primer dilution 1:10:<br />
+      Primers 95 &amp; 54 from Florian  Altegoer were diluted 1:10 by mixing 10&micro;L of primers with 90&micro;L milipore water  each.</p>
+	  <table width="100%" border="1">
+      <tr>
+        <th scope="col">Mix [&micro;l]</th>
+        <th scope="col">1 attempt with phusion</th>
+        <th scope="col">One attempt with Q5 mastermix</th>
+      </tr>
+      <tr>
+        <th scope="row">Pet24d-cup1-1<br />1:10 dilution</th>
+        <td>1</td>
+        <td>1</td>
+      </tr>
+      <tr>
+        <th scope="row">Primer 54Flo</th>
+        <td>1</td>
+        <td>1</td>
+      </tr>
+      <tr>
+        <th scope="row">Primer 56Flo</th>
+        <td>1</td>
+        <td>1</td>
+      </tr>
+      <tr>
+        <th scope="row">Phusion</th>
+        <td>1</td>
+        <td>-</td>
+      </tr>
+      <tr>
+        <th scope="row">Phusion Buffer 5x</th>
+        <td>10</td>
+        <td>-</td>
+      </tr>
+      <tr>
+        <th scope="row">dNTP Mix</th>
+        <td>1</td>
+        <td>-</td>
+      </tr>
+      <tr>
+        <th scope="row">Water</th>
+        <td>35</td>
+        <td>22</td>
+      </tr>
+      <tr>
+        <th scope="row">Q5 Mastermix</th>
+        <td>-</td>
+        <td>25</td>
+      </tr>
+      <tr>
+        <th scope="row">Total Volume</th>
+        <td>50</td>
+        <td>20</td>
+      </tr>
+    </table>
+    <br />
+  	<table width="100%" border="1">
+  <tr>
+    <th scope="col">Step</th>
+    <th scope="col">Temperature &deg;C</th>
+    <th scope="col">Time</th>
+  </tr>
+  <tr>
+    <th scope="row">1</th>
+    <td>98</td>
+    <td>3 min</td>
+  </tr>
+  <tr>
+    <th scope="row">2</th>
+    <td>98</td>
+    <td>30 sec</td>
+  </tr>
+  <tr>
+    <th scope="row">3</th>
+    <td>55</td>
+    <td>30 sec</td>
+  </tr>
+  <tr>
+    <th scope="row">4</th>
+    <td>72</td>
+    <td>2 min</td>
+  </tr>
+  <tr>
+    <th scope="row">5</th>
+    <td>Go To 2</td>
+    <td>30x</td>
+  </tr>
+  <tr>
+    <th scope="row">6</th>
+    <td>72</td>
+    <td>4min</td>
+  </tr>
+  <tr>
+    <th scope="row">7</th>
+    <td>8</td>
+    <td>infinite</td>
+  </tr>
+</table>
+	<p>PCR was run overnight.</p>
+    </div>
+</fieldset>
+<fieldset class="exp19">
+    <legend><a name="exp19.2">19.2 Restriction digest of pet24d with Nco1 and BamH1</a></legend>
+    <div class="aim">
+    <p>Aim: Creating Nco/ Bam restriction sites in pet24d for cloning PCR fragments amplified with primers flo56 and flo54 which contain Nco/Bam sites as well.</p>
+    </div>
+    <div class="exp-content">
+    <p>Prepped pet24d was cut with Nco1 and BamH1 in order to create restriction sites for ligating the Flagellin/ Hag-Domain fragments into the vector. The Hag-fragments which were amplified via PCR with primers flo54 and 56 contain Nco1/ BamH1 restriction sites for that purpose as well.</p>
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Component</th>
+    <th scope="col">Volume [&micro;l]</th>
+  </tr>
+  <tr>
+    <th scope="row">Pet24d (148 ng/&micro;L)</th>
+    <td>7</td>
+  </tr>
+  <tr>
+    <th scope="row">Cutsmart 10x</th>
+    <td>2</td>
+  </tr>
+  <tr>
+    <th scope="row">Nco1</th>
+    <td>0,5</td>
+  </tr>
+  <tr>
+    <th scope="row">BamH1</th>
+    <td>0,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Water</th>
+    <td>10</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>20</td>
+  </tr>
+</table>
+	<p>Incubation for 1h at 37&deg;C and heat shocked at 80&deg;C.</p>
+    </div>
+</fieldset>
+<fieldset class="exp15">
+    <legend><a name="exp15.52">15.52 Miniprep of different plasmids</a></legend>
+    <div class="aim">
+    <p>Aim: Receiving more plasmid DNA for further experiments</p>
+    </div>
+    <div class="exp-content">
+    <p>Colonies were picked from plates and 8ml LB with necessary antibiotics each inoculated, followed by incubation at 37&deg;C overnight.</p>
+    <p>Clones were picked from plates with plasmids:</p>
+    <ul class="list">
+      <li>Pet24d-Fla-Cup1-1 (piGEM-006)</li>
+      <li>pMAD-Hag-Flank (piGEM-005)</li>
+      <li>pMAD-Hag-Flank -Cup1-1 (piGEM-016)</li>
+      <li>pEX-A2+DARPin (piGEM-017)</li>
+    </ul>
+    </div>
+</fieldset>
+</div>
+<!-- 07.06.14 -->
+<div class="notebooky-entry">
+<h2 class="title">
+	<a name="07.062014">07.062014</a>
+</h2>
+<fieldset class="exp15">
+    <legend><a name="exp15.53">15.53 Sequencing pMAD-fla-cup1-1 </a></legend>
+    <div class="exp-content">
+    <p>The sequencing showed the correct insertion of the cup-1-1 gene into the hag-flank construct but contained a stop codon which was not removed by the used reverse primer. Unfortunately we used primers for amplification of the whole cup1-1 gene and not just for the truncated gene coding  for the metallothionein domain only. Therefore new primers had to be designed an the gibson assembly for integration of the metallothionein domain into pMAD and pet24d has to be repeated.</p>
+    </div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.6">18.6 gel extraction & purification of DARPin gene </a></legend>
+    <div class="aim">
+    <p>Aim: Receiving DARPin gene with spe1 sites for ligation into linearized piGEM-005</p>
+    </div>
+    <div class="exp-content">
+    <p>The with Spe1 digested pEX-A2 was purified via electrophoresis with an 1% agarose gel in order to divide pEX-A2 backbone and the DARPin gene (489 bp). The digest attempt was splitted and loaded into two pockets to be sure not to overload the gel. The correct bands were cut out and the DNA fragment was rescued according to the protocol of our OMEGA gel extraction kit.</p>
+    <img src="https://static.igem.org/mediawiki/2014/a/a0/MR_2014-06-07_DARPin.jpg" width="20%"/>
+    <p>Expected bands:<br />
+      DARPin gene: 489 bp<br />
+      pEX-A2 backbone: 1961bp<br />
+      The concentration after gel  extraction: 9 ng/&micro;l</p>
+    </div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.7">18.7 Ligation of DARPin gene and linearized piGEM-005</a></legend>
+    <div class="aim">
+    <p>Aim: Ligation of DARPin- (from 18.6) into Spe1 cut piGEM-005 from 18.5 for integration of the DARPin-Flagellin construct into Bacillus subtilis chromosome</p>
+    </div>
+    <div class="exp-content">
+    <p>The DARPin gene with Spe1 sites was used as insert for the ligation into linearized pMAD (from 18.5) which contains the designed Spe1 site. The ligation attempt was done twofold and calculated by the Ligation Calculator from the iGEM-Team Texas in 2011:</p>
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Component</th>
+    <th scope="col">Volume [&micro;l]</th>
+  </tr>
+  <tr>
+    <th scope="row">Insert (DARPin, c= 9 ng/&micro;L)</th>
+    <td>2</td>
+  </tr>
+  <tr>
+    <th scope="row">Vector (piGEM-005, c=4ng/&micro;L)</th>
+    <td>10</td>
+  </tr>
+  <tr>
+    <th scope="row">Ligase-Buffer 10x</th>
+    <td>2</td>
+  </tr>
+  <tr>
+    <th scope="row">T4 Ligase</th>
+    <td>1</td>
+  </tr>
+  <tr>
+    <th scope="row">Milipore water</th>
+    <td>5</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>20</td>
+  </tr>
+</table>
+	<p>Incubation was performed overnight at room temperature.</p>
+    </div>
+</fieldset>
+<fieldset class="exp13">
+    <legend><a name="exp13.63">13.63 checking Bacillus WT 3610  growth on 5&micro;g/&micro;L CM</a></legend>
+    <div class="aim">
+    <p>Aim: check if wildtype has a resistance against CM </p>
+    </div>
+    <div class="exp-content">
+    <p>Result: <em>Bacillus subtilis</em> Wildtype 3610 grew on the CM plate.</p>
+    <p>In order to make out if a selection is possible WT3610 was plated out  from an LB plate (13.62)&nbsp; on 25 ng/ &micro;L CM  to check were Bacillus CM threshold is.</p>
+    <p>Incubation at 30&deg;C over the weekend.</p>
+	</div>
+</fieldset>
+</div>
+<!-- 08.06.14 -->
+<div class="notebooky-entry">
+<h2 class="title">
+	<a name="08.06.2014">08.06.2014</a>
+</h2>
+<fieldset class="exp18">
+    <legend><a name="exp18.8">18.8 new Spe1 restriction of DARPin-gene in pEX-A2 & pMAD-hag-flank (piGEM-005)</a></legend>
+    <div class="aim">
+    <p>Aim: Receiving new insert and vector in case of an unsuccessful ligation for further attempts. </p>
+    </div>
+    <div class="exp-content">
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Restriction</th>
+    <th scope="col">pEX-A2-DARPin digest (&micro;l)</th>
+    <th scope="col">pMAD-Hag-Flank digest (&micro;l)</th>
+    <th scope="col">Spe1-Mastermix</th>
+  </tr>
+  <tr>
+    <th scope="row">pEX-A2+DARPin (398 &micro;g/&micro;L)</th>
+    <td>10 = ca. 4&micro;g</td>
+    <td>-</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">pMAD-Fla (150 &micro;g/&micro;L)</th>
+    <td>-</td>
+    <td>7= ca. 1 &micro;g</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">SpeI</th>
+    <td>-</td>
+    <td>-</td>
+    <td>1</td>
+  </tr>
+  <tr>
+    <th scope="row">CutSmart-Buffer (10x)</th>
+    <td>-</td>
+    <td>-</td>
+    <td>2,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Water</th>
+    <td>-</td>
+    <td>-</td>
+    <td>21,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Mastermix</th>
+    <td>10</td>
+    <td>13</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>20</td>
+    <td>20</td>
+    <td>25</td>
+  </tr>
+</table>
+	<p>Incubation was performed for 2h at 37&deg;C and heat inactivated at 80&deg;C for  5 minutes.</p>
+	</div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.9">18.9 Transformation of overnight ligation from 18.7</a></legend>
+    <div class="exp-content">
+    <p>The whole 20&micro;L attempt from the  overnight ligations were transformed into <em>E.Coli  XL1-Blue</em> and plated on LB-Amp plates.&nbsp;  Additionally a negative control was created by transforming 1&micro;L Spe1 cut  piGEM-005 into <em>E.Coli XL1-Blue </em>as  well.</p>
+	</div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.10">18.10 Gel extraction for isolation of DARPin gene out of pEX-A2</a></legend>
+    <div class="aim">
+    <p>Aim: Receiving new insert in case of an unsuccessful ligation for further attempts like in 18.6</p>
+    </div>
+    <div class="exp-content">
+    <p>The with Spe1 digested pEX-A2 was  purified via electrophoresis with an 1% agarose gel like in 18.6. The band correct bands were cut out and the DNA fragment was rescued according to the  protocol of our OMEGA gel extraction kit.</p>
+    <img src="https://static.igem.org/mediawiki/2014/1/16/MR_2014-06-08_Darpin.jpg" width="20%" />
+    <p>Expected bands:<br />
+      DARPin gene: 489 bp<br />
+      pEX-A2 backbone: 1961bp<br />
+      The concentration after gel extraction: 10 ng/&micro;l</p>
+    </div>
+</fieldset>
+</div>
+<!-- 09.06.14 -->
+<div class="notebooky-entry">
+<h2 class="title">
+	<a name="09.06.2014">09.06.2014</a>
+</h2>
+<fieldset class="exp18">
+    <legend><a name="exp18.12">18.12 Checking Transformation of overnight ligation from 18.7 </a></legend>
+    <div class="exp-content">
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Plate</th>
+    <th scope="col">Amount of colonies</th>
+  </tr>
+  <tr>
+    <th scope="row">Negative control</th>
+    <td>6</td>
+  </tr>
+  <tr>
+    <th scope="row">Ligation attempt 1</th>
+    <td>7</td>
+  </tr>
+  <tr>
+    <th scope="row">Ligation attempt 2</th>
+    <td>0</td>
+  </tr>
+</table>
+    </div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.13">18.13 Checking success of ligation via cPCR</a></legend>
+    <div class="aim">
+    <p>Aim: A cPCR with the primers 54 and 56 shows the success of ligation by amplification of the Hag-construct.</p>
+    </div>
+    <div class="exp-content">
+      <p>In order to check the positive  insertion of the DARPin gene into pMAD a PCR amplification with primers 54 and  56 for the flagellin should generate an ca. 1500 bp fragment on the gel.  Negative clones would show still just a 1000 bp band because of the  amplification of the Hag-Spe1 site construct. The picked  clones were transferred on a new LB-amp plate.</p>
+      <table width="100%" border="1">
+  <tr>
+    <th scope="col">Mix</th>
+    <th scope="col">Master-Mix for 7 attempts (&micro;L)</th>
+    <th scope="col">Mix for PCR attempt (&micro;L)</th>
+  </tr>
+  <tr>
+    <th scope="row">Colony</th>
+    <td>-</td>
+    <td>part of a colony</td>
+  </tr>
+  <tr>
+    <th scope="row">Primer Flo 54</th>
+    <td>3,5</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Primer Flo 56</th>
+    <td>3,5</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Phusion</th>
+    <td>7</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Phusion Buffer 5x</th>
+    <td>28</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">dNTP Mix</th>
+    <td>3,5</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Water</th>
+    <td>94,5</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Mastermix</th>
+    <td>-</td>
+    <td>20</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>140</td>
+    <td>20</td>
+  </tr>
+</table>
+	<p>Expected bands:<br />
+	  Hag-DARPin-construct: ca. 1500 bp</p>
+      <img src="https://static.igem.org/mediawiki/2014/7/70/MR_2014-06-09_DARPin.jpg" width="30%" />
+      <p>The gel shows bands at 1000 which means that the clones contain just relegated pMAD vector and are all negative.
+The ligation had to be repeated.</p>
+</div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.14">18.14 Dephosphorylation of linearized piGEM-005</a></legend>
+    <div class="aim">
+    <p>Aim: Dephosphorylation of 5’-end with antarctic phosphatase in order to decrease the religation of the linearized piGEM-005 from 18.8</p>
+    </div>
+    <div class="exp-content">
+    <p>The cut Spe1 cut piGEM-005 was dephosporylated at the 5’-end with Antarctic phosphatase to prevent the vector from relegation.</p>
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Component</th>
+    <th scope="col">Volume [&micro;l]</th>
+  </tr>
+  <tr>
+    <th scope="row">Vector (piGEM-005, c=148  ng/&micro;L)</th>
+    <td>20 (=ca. 2 &micro;g)</td>
+  </tr>
+  <tr>
+    <th scope="row">Antarctic phos.-Buffer 10x</th>
+    <td>3</td>
+  </tr>
+  <tr>
+    <th scope="row">Antarctic phosphatase</th>
+    <td>1</td>
+  </tr>
+  <tr>
+    <th scope="row">Milipore Water</th>
+    <td>6</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>30</td>
+  </tr>
+</table>
+    <p>The sample was incubated for 1h at 37&deg;C at heat inactivated at 70&deg;C for  10minutes.</p>
+    </div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.15">18. new ligation of linearized/ dephosphorylized piGEM-005 &  DARPin gene</a></legend>
+    <div class="aim">
+    <p>Aim: Dephosphorylation piGEM-005 was ligated with extracted DARPin gene again</p>
+    </div>
+    <div class="exp-content">
+    <p>Because of the negative colony PCR from 18.13 a new ligation with dephosphorylized piGEM-005 from 18.14 and new extracted DARPin gene from 18.10 was performed in 2 attempts.</p>
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Component</th>
+    <th scope="col">Volume [&micro;l]</th>
+  </tr>
+  <tr>
+    <th scope="row">Insert (DARPin, c= 10  ng/&micro;L)</th>
+    <td>12,4</td>
+  </tr>
+  <tr>
+    <th scope="row">Vector (piGEM-005, c= 148  ng/&micro;L)</th>
+    <td>4,6</td>
+  </tr>
+  <tr>
+    <th scope="row">Ligase-Buffer 10x</th>
+    <td>2</td>
+  </tr>
+  <tr>
+    <th scope="row">T4 Ligase</th>
+    <td>1</td>
+  </tr>
+  <tr>
+    <th scope="row">Milipore Water</th>
+    <td>5</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>20</td>
+  </tr>
+</table>
+	<p>Incubation 3h at room temperature</p>
+    </div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.16">18.16 Transformation of overnight ligation from 18.15</a></legend>
+    <div class="exp-content">
+    <p>The whole 20&micro;L attempt from the  ligations (18.15) were transformed into <em>E.Coli  XL1-Blue</em> and plated on LB-Amp plates.&nbsp;  Additionally a negative control was created by transforming 1&micro;L Spe1 cut  piGEM-005 into <em>E.Coli XL1-Blue </em>as  well.</p>
+	</div>
+</fieldset>
+<fieldset class="exp13">
+    <legend><a name="exp13.64">13.64 checking Bacillus WT 3610 growth on 5, 10 & 15 &micro;g/&micro;L CM</a></legend>
+    <div class="aim">
+    <p>Aim: check if wildtype has a resistance against CM </p>
+    </div>
+    <div class="exp-content">
+    <p>Result: <em>Bacillus subtilis</em> Wildtype 3610 did not grow on the 25 ng/µLCM plate</p>
+    <p>In order to check at which concentration CM Bacillus cannot survive he  was plated out from an LB plate on LB-CM plates with different CM  concentrations (5, 10, 15 ng/mL).</p>
+    <p>Incubation at 30&deg;C over night.</p>
+    </div>
+</fieldset>
+</div>
+<!-- 10.06.14 -->
+<div class="notebooky-entry">
+<h2 class="title">
+	<a name="10.06.2014">10.06.2014</a>
+</h2>
+<fieldset class="exp18">
+    <legend><a name="exp18.17">18.17 Checking Transformation of ligation from 18.16</a></legend>
+    <div class="exp-content">
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Plate</th>
+    <th scope="col">Amount of colonies</th>
+  </tr>
+  <tr>
+    <th scope="row">Negative control</th>
+    <td>1</td>
+  </tr>
+  <tr>
+    <th scope="row">Ligation attempt 1</th>
+    <td>2</td>
+  </tr>
+  <tr>
+    <th scope="row">Ligation attempt 2</th>
+    <td>&gt;80</td>
+  </tr>
+</table>
+    </div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.18">18.18 Checking success of ligation via cPCR</a></legend>
+    <div class="aim">
+    <p>Aim: A cPCR with the primers 54 and 56 shows the success of ligation by amplification of the Hag-construct.</p>
+    </div>
+    <div class="exp-content">
+    <p>In order to check the positive  insertion of the DARPin gene into pMAD a PCR amplification with primers 54 and  56 for the flagellin should generate an ca. 1500 bp fragment on the gel.  Negative clones would show still just a 1000 bp band because of the  amplification of the Hag-Spe1 site construct. The picked  clones were transferred on a new LB-amp plate. 12 clones were picked.</p>
+          <table width="100%" border="1">
+  <tr>
+    <th scope="col">Mix</th>
+    <th scope="col">Master-Mix for 14 attempts (&micro;L)</th>
+    <th scope="col">Mix for PCR attempt (&micro;L)</th>
+  </tr>
+  <tr>
+    <th scope="row">Colony</th>
+    <td>-</td>
+    <td>part of a colony</td>
+  </tr>
+  <tr>
+    <th scope="row">Primer Flo 54</th>
+    <td>7</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Primer Flo 56</th>
+    <td>7</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Phusion</th>
+    <td>14</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Phusion Buffer 5x</th>
+    <td>56</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">dNTP Mix</th>
+    <td>7</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Water</th>
+    <td>189</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Mastermix</th>
+    <td>-</td>
+    <td>20</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>280</td>
+    <td>20</td>
+  </tr>
+</table>
+	<br />
+       <table width="100%" border="1">
+  <tr>
+    <th scope="col">Step</th>
+    <th scope="col">Temperature &deg;C</th>
+    <th scope="col">Time</th>
+  </tr>
+  <tr>
+    <th scope="row">1</th>
+    <td>98</td>
+    <td>3 min</td>
+  </tr>
+  <tr>
+    <th scope="row">2</th>
+    <td>98</td>
+    <td>30 sec</td>
+  </tr>
+  <tr>
+    <th scope="row">3</th>
+    <td>55</td>
+    <td>1min 45sec</td>
+  </tr>
+  <tr>
+    <th scope="row">4</th>
+    <td>72</td>
+    <td>1 min</td>
+  </tr>
+  <tr>
+    <th scope="row">5</th>
+    <td>Go To 2</td>
+    <td>30x</td>
+  </tr>
+  <tr>
+    <th scope="row">6</th>
+    <td>72</td>
+    <td>4min</td>
+  </tr>
+  <tr>
+    <th scope="row">7</th>
+    <td>8</td>
+    <td>infinite</td>
+  </tr>
+</table>
+	<p><img src="https://static.igem.org/mediawiki/2014/4/4d/MR_2014-06-10_Darpin.jpg" width="40%" /></p>
+    <p>Expected bands:<br />
+      Hag-DARPin-construct: ca. 1500 bp</p>
+      <p>Clone 1, 2, 3, 4, 5, 7, 9, 11 and 12 were the positive clones at 1500 bp.</p>
+</div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.9">18.19 Miniprep of positive clones</a></legend>
+    <div class="aim">
+    <p>Aim: In order to check the orientation of the positive clones minipreps were inoculated for further experiments</p>
+    </div>
+    <div class="exp-content">
+    <p>Because of the ligation via 2  Spe1 sites the chance is 50:50 that the clones contain the  pMAD-Hag-Flank-DARPin construct in the right orientation (Startcodon on the  Hag1-site). For test digests the plasmids have to be amplified by minipreps. </p>
+    <p>The clones were used to inoculate  7 mL LB-Amp and incubated at 37&deg;C Overnight.</p>
+</div>
+</fieldset>
+<fieldset class="exp13">
+    <legend><a name="exp13.64">13.64 checking Bacillus WT 3610 growth on 25 & 35 &micro;g/&micro;L CM</a></legend>
+    <div class="aim">
+    <p>Aim: check if wildtype has a resistance against CM </p>
+    </div>
+    <div class="exp-content">
+    <p>Result: Bacillus subtilis Wildtype 3610 grew on the 5, 10 & 15&micro;g//&micro;l LB-CM plate.</p>
+    <p>We saw that Bacillus grew on almost every CM concentration except 25  &micro;g/&micro;L. So we transformed competent WT3610 with Nose plasmid piGEM-003 as a  positive control and plated them out on LB-CM with 25 &micro;g/&micro;L and 35 &micro;g/&micro;L from  Daniel Schindler.</p>
+    <p>Additionally WT from Felix Dempwolff which was made competent was also  transformed with piGEM-004 was plated out on LB-CM with 5, 10 and 15 &micro;g/mL CM  to check if these cells can be selected better. </p>
+    <p>Incubation at 30&deg;C for 2 days.</p>
+</div>
+</fieldset>
+</div>
+<!-- 12.06.14 -->
+<div class="notebooky-entry">
+<h2 class="title">
+	<a name="12.06.2014">12.06.2014</a>
+</h2>
+<fieldset class="exp18">
+    <legend><a name="exp18.19">18.19 Miniprep of positive clones</a></legend>
+    <div class="exp-content">
+    <p>The concentration of the prepped plasmids was between 100 and 150 ng/&micro;L.</p>
+    </div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.20">18.20 Test digest with EcoRV </a></legend>
+    <div class="aim">
+    <p>Aim: Checking the right orientation of the prepped plasmids</p>
+    </div>
+    <div classs="exp-content">
+    <p>The plasmids from the positive clones were digested with EcoRV so that specific fragments emerge when cutting into the DARPin gene and the vector backbone.</p>
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Component</th>
+    <th scope="col">Volume [&micro;l]</th>
+    <th scope="col">Mastermix for 10 attempts [&micro;l]</th>
+  </tr>
+  <tr>
+    <th scope="row">Plasmid of clone</th>
+    <td>2 (ca. 200ng)</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Cutsmart 10x</th>
+    <td>-</td>
+    <td>8</td>
+  </tr>
+  <tr>
+    <th scope="row">EcoRV</th>
+    <td>-</td>
+    <td>1</td>
+  </tr>
+  <tr>
+    <th scope="row">Milipore water</th>
+    <td>-</td>
+    <td>71</td>
+  </tr>
+  <tr>
+    <th scope="row">Mastermix</th>
+    <td>8</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>10</td>
+    <td>80</td>
+  </tr>
+</table>
+    <p>Right orientation:&nbsp;&nbsp;&nbsp; 7900 &ndash; <strong>1570</strong> &ndash; 2500 &ndash; <strong>55</strong><br />
+      Wrong orientation: 7900 &ndash;<strong> 1170 </strong>&ndash; 2500 &ndash; <strong>460 </strong></p>
+      <img src="https://static.igem.org/mediawiki/2014/a/ac/MR_2014-06-11_Darpin.jpg" width="40%" />
+      <p>Clone 1, 2, 3, 4, 7, 9 and 11 have the right orientation.</p>
+</div>
+</fieldset>
+</div>
+<!-- 12.06.14 -->
+<div class="notebooky-entry">
+<h2 class="title">
+	<a name="12.06.2014">12.06.2014</a>
+</h2>
+<fieldset class="exp18">
+    <legend><a name="exp18.21">18.21 PCR with pMAD-Hag-Flank-DARPin (piGEM-019) and piGEM-005</a></legend>
+    <div class="aim">
+    <p>Aim: Amplification  of Hag-Spe1-construct and Hag-DARPin construct with Nco1/BamH1 sites for  cloning into pet24d &rarr; crystallization of domains.</p>
+	</div>
+    <div class="exp-content">
+    <p>The  templates (piGEM-005, prepped pasmid from clone 7 &amp; 12 ) were diluted 1:10.  piGEM-005 should function as a negative control. Clone 12 was picked in case  the second orientation could be used for different experiments. 5 &micro;L PCR  product + 1 &micro;L loading dye were analysed on an 1% agarose gel.</p>
+              <table width="100%" border="1">
+  <tr>
+    <th scope="col">Mix</th>
+    <th scope="col">Volume</th>
+    </tr>
+  <tr>
+    <th scope="row">Template 1:10</th>
+    <td>1</td>
+    </tr>
+  <tr>
+    <th scope="row">Primer Flo 54</th>
+    <td>1</td>
+    </tr>
+  <tr>
+    <th scope="row">Primer Flo 56</th>
+    <td>1</td>
+    </tr>
+  <tr>
+    <th scope="row">Phusion</th>
+    <td>1</td>
+    </tr>
+  <tr>
+    <th scope="row">Phusion Buffer 5x</th>
+    <td>10</td>
+    </tr>
+  <tr>
+    <th scope="row">dNTP Mix</th>
+    <td>1</td>
+    </tr>
+  <tr>
+    <th scope="row">Water</th>
+    <td>35</td>
+    </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>50</td>
+  </tr>
+</table>
+	<br />
+       <table width="100%" border="1">
+  <tr>
+    <th scope="col">Step</th>
+    <th scope="col">Temperature &deg;C</th>
+    <th scope="col">Time</th>
+  </tr>
+  <tr>
+    <th scope="row">1</th>
+    <td>98</td>
+    <td>3 min</td>
+  </tr>
+  <tr>
+    <th scope="row">2</th>
+    <td>98</td>
+    <td>30 sec</td>
+  </tr>
+  <tr>
+    <th scope="row">3</th>
+    <td>55</td>
+    <td>1min 45sec</td>
+  </tr>
+  <tr>
+    <th scope="row">4</th>
+    <td>72</td>
+    <td>2 min</td>
+  </tr>
+  <tr>
+    <th scope="row">5</th>
+    <td>Go To 2</td>
+    <td>30x</td>
+  </tr>
+  <tr>
+    <th scope="row">6</th>
+    <td>72</td>
+    <td>4min</td>
+  </tr>
+  <tr>
+    <th scope="row">7</th>
+    <td>8</td>
+    <td>infinite</td>
+  </tr>
+</table>
+	</div>
+    <img src="https://static.igem.org/mediawiki/2014/4/47/MR_2014-06-12_piGEM-005.jpg" width="20%" />
+    <p>Expected  bands:<br />
+  &nbsp;clone 7 &amp; 12 PCR product at ca. 1500bp &ndash;  piGEM-005 PCR product at 1kb</p>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.22">18.22 restriction digest of Hag PCR fragments from 18.21 with Nco1/ BamH1</a></legend>
+    <div class="aim">
+    <p>Aim: creating restriction sites for cloning into pet24d cut with Nco/Bam</p>
+    </div>
+    <div class="exp-content">
+    <p>The PCR  products from 18.21 were digested with Nco1 and BamH1 to create restriction  sites in order to ligate the fragments into Nco/Bam cut pet24d.</p>
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Component</th>
+    <th scope="col">Volume [&micro;l]</th>
+  </tr>
+  <tr>
+    <th scope="row">PCR products</th>
+    <td>45</td>
+  </tr>
+  <tr>
+    <th scope="row">Cutsmart 10x</th>
+    <td>5,2</td>
+  </tr>
+  <tr>
+    <th scope="row">Nco1</th>
+    <td>1</td>
+  </tr>
+  <tr>
+    <th scope="row">BamH1</th>
+    <td>1</td>
+  </tr>
+  <tr>
+    <th scope="row">Water</th>
+    <td>2,8</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>52</td>
+  </tr>
+</table>
+	<p>&nbsp;Incubation for 2h at 37&deg;C with heat shock at  80&deg;C.</p>
+</div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.23">18.23 Ligation of pet24d and Hag PCR fragments from 18.22 cut with Nco/Bam</a></legend>
+    <div class="aim">
+    <p>Aim: cloning inserts into pet24d for crystallization</p>
+    </div>
+    <div class="exp-content">
+    <p>The Nco/cut Flagellin PCR products from 18.22 (from clone 7 and piGEM-005) were ligated with Nco1 and BamH1 cut pet24d. </p>
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Component</th>
+    <th scope="col">Pet-Hag attempt (&micro;L)</th>
+    <th scope="col">Pet-Hag-DARPin attempt (&micro;L)</th>
+  </tr>
+  <tr>
+    <th scope="row">Insert (PCR fragments , c= ca. 400 ng/&micro;L)</th>
+    <td>2</td>
+    <td>2</td>
+  </tr>
+  <tr>
+    <th scope="row">Vector (pet24d, c= 50ng/&micro;L)</th>
+    <td>5</td>
+    <td>5</td>
+  </tr>
+  <tr>
+    <th scope="row">Ligase-Buffer 10x</th>
+    <td>2</td>
+    <td>2</td>
+  </tr>
+  <tr>
+    <th scope="row">T4 Ligase</th>
+    <td>1</td>
+    <td>1</td>
+  </tr>
+  <tr>
+    <th scope="row">Milipore Water</th>
+    <td>10</td>
+    <td>10</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>20</td>
+    <td>20</td>
+  </tr>
+</table>
+	<p>Incubation overnight at room temperature.</p>
+    </div>
+</fieldset>
+<fieldset class="exp20">
+    <legend><a name="exp20.2">20.2 Transformation of competent <em>Bacillus subtilis</em></a></legend>
+    <div class="aim">
+    <p>Aim: transformation of plasmid into Bacillus subtilis WT3610</p>
+    </div>
+    <div class="exp-content">
+    <p>100 &micro;L  of overnight culture were added to 10 mL of MNGE-Medium and incubated till an  OD of 1,1-1,3 at 37&deg;C which could take 4-5h.</p>
+    <p>After  reaching OD of 1,1-1,3 2 x 400 &micro;L of the culture were transformed with 1,5 &micro;g  piGEM-005 and -018. After 1h incubation at 37&deg;C 100 &micro;L Expression mix were  added and incubated for 1h as well.</p>
+    <p>In the  end the 500 &micro;L attempt was plated out on MLS-X-Gal plates and incubated at 30  &deg;C overnight until colonies could be seen. </p>
+</div>
+</fieldset>
+</div>
+<!-- 13.06.14 -->
+<div class="notebooky-entry">
+<h2 class="title">
+	<a name="13.06.2014">13.06.2014</a>
+</h2>
+<fieldset class="exp18">
+    <legend><a name="exp18.24">18.24 Transformation of overnight ligation</a></legend>
+    <div class="aim">
+    <p>Aim: checking success of ligation and amplification of ligated construct</p>
+    </div>
+    <div class="exp-content">
+    <p>The  whole 20&micro;L attempt was transformed into E.Coli X1-Blue, plated out on LB-Can  plates and incubated at 37&deg;C overnight.</p>
+</div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.25">18.25 Miniprep of pMAD-Hag-Flank-DARPin (piGEM-018)</a></legend>
+    <div class="aim">
+    <p>Aim: Amplification of plasmids for work and storage</p>
+    </div>
+    <div class="exp-content">
+    <p>2x 6 mL of LB-Amp were inoculated  with a colony from apiGEM-018 transformation plate and incubated at 37&deg;C  overnight. </p>
+</div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.26">18.26 sequencing of constructs</a></legend>
+    <div class="aim">
+    <p>Aim: checking the right insertion into the plasmids</p>
+    </div>
+    <div class="exp-content">
+    <p>pMAD-Hag-Flank-DARPin and the  hormone receptor clone 1 were given away in form of a premix with primers for  sequencing. 10 &micro;L with 50-100 ng/&micro;L were mixed with 2 &micro;L of primers for  sequencing according to the following scheme:</p>
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Premix</th>
+    <th scope="col">Label-Nr.</th>
+    <th scope="col">Construct</th>
+    <th scope="col">Primer</th>
+  </tr>
+  <tr>
+    <th scope="row">1</th>
+    <td>391</td>
+    <td>pMAD-Hag-Flank-DARPin</td>
+    <td>Flo54 (Hag-F-Nco)</td>
+  </tr>
+  <tr>
+    <th scope="row">2</th>
+    <td>392</td>
+    <td>pMAD-Hag-Flank-DARPin</td>
+    <td>Flo56 (Hag-R-Bam)</td>
+  </tr>
+  <tr>
+    <th scope="row">3</th>
+    <td>393</td>
+    <td>pRSGII426+receptor  gene</td>
+    <td>TW248</td>
+  </tr>
+  <tr>
+    <th scope="row">4</th>
+    <td>394</td>
+    <td>pRSGII426+receptor  gene</td>
+    <td>TW249</td>
+  </tr>
+</table>
+</div>
+</fieldset>
+<fieldset class="exp13">
+    <legend><a name="exp13.65">13.65 checking Bacillus WT from Felix Dempwolff growth</a></legend>
+    <div class="aim">
+    <p>Aim: check which WT can used for selection with Nose plasmids</p>
+    </div>
+    <div class="exp-content">
+    <p></p>
+    <p>Competent WT from Felix Dempwolff was transformed with piGEM-002, -003  and -004 by incubating the aliquods with 5 &micro;L plasmid for 30 min at 37&deg;C. After  half an hour the whole attempt was plated out on LB-Cm (5 ng/&micro;L). </p>
+    <p>Incubation at 30&deg;C for 2 days.</p>
+</div>
+</fieldset>
+</div>
+<!-- 14.06.14 -->
+<div class="notebooky-entry">
+<h2 class="title">
+	<a name="14.06.2014">14.06.2014</a>
+</h2>
+<fieldset class="exp18">
+    <legend><a name="exp18.27">18.27 miniprep of inoculated plasmids from 18.25</a></legend>
+    <div class="aim">
+    <p>Aim: isolation of plasmids</p>
+    </div>
+    <div class="exp-content">
+    <p>The miniprep of pMAD-Hag-Flank-DARPin was done according to the protocol of the OMEGA DNA kit. </p>
+    </div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.28">18.28 pet24d digest with Nco/Bam</a></legend>
+    <div class="aim">
+    <p>Aim: preparing vector for new ligation attempts</p>
+    </div>
+    <div class="exp-content">
+    <p>Because of the unsuccessful ligation from 18.23 new vector (pet24d) was cut with Nco1 and BamH1 according to the following scheme: </p>
+       <table width="100%" border="1">
+  <tr>
+    <th scope="col">Component</th>
+    <th scope="col">Volume [&micro;l]</th>
+  </tr>
+  <tr>
+    <th scope="row">Pet24d (148 ng/&micro;L)</th>
+    <td>15</td>
+  </tr>
+  <tr>
+    <th scope="row">Cutsmart 10x</th>
+    <td>3</td>
+  </tr>
+  <tr>
+    <th scope="row">Nco1</th>
+    <td>0,5</td>
+  </tr>
+  <tr>
+    <th scope="row">BamH1</th>
+    <td>0,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Water</th>
+    <td>6</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>30</td>
+  </tr>
+</table>
+	<p>Incubation at 37&deg;C for 2h.</p>
+    </div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.29">18.29 Pst1 digest of PCR fragments from piGEM-018 with Hag-primers</a></legend>
+    <div class="aim">
+    <p>Aim: checking if the correct inserts are used for ligation </p>
+    </div>
+    <div class="exp-content">
+    <p>The DARPin-Hag  constructs contain a Pst1 restriction site which could be used to check if the  DARPin gene was inserted into the Hag-construct correctly again. For that  purpose PCR products based on piGEM-018 from clone 7 and 12 (right and wrong  orientation) as a template were cut with Pst1. </p>
+    <p>PCR  products from clone 7: 658 bp and 781 bp fragment.</p>
+    <p>&nbsp;PCR products from clone 12:1000bp and 429 bp  fragments.</p>
+     <table width="100%" border="1">
+  <tr>
+    <th scope="col">Component</th>
+    <th scope="col">Volume [&micro;l]</th>
+  </tr>
+  <tr>
+    <th scope="row">PCR fragment (350 ng/&micro;L)</th>
+    <td>3</td>
+  </tr>
+  <tr>
+    <th scope="row">Cutsmart 10x</th>
+    <td>1</td>
+  </tr>
+  <tr>
+    <th scope="row">Pst1</th>
+    <td>0,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Water</th>
+    <td>5,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>10</td>
+  </tr>
+</table>
+	<p>Incubation at 37&deg;C for 2h.</p>
+    <img src="https://static.igem.org/mediawiki/2014/7/79/MR_2014-06-14_piGEM-018.jpg" width="20%" />
+</div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.30">18.30 PCR amplification of DARPin-Hag and Hag fragment</a></legend>
+    <div class="aim">
+    <p>Aim: amplification of DARPin-Hag fragments for repeating the ligation </p>
+    </div>
+    <div class="exp-content">
+    <p>piGEM-018 & -005 were used as template for a PCR with the primers from Florian Altegoer 54 and 56. The products could be used for further cloning after Nco/Bam digest.</p>
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Mix</th>
+    <th scope="col">Volume</th>
+    </tr>
+  <tr>
+    <th scope="row">Template (piGEM-005 &amp; -018)</th>
+    <td>1</td>
+    </tr>
+  <tr>
+    <th scope="row">Primer Flo 54</th>
+    <td>1</td>
+    </tr>
+  <tr>
+    <th scope="row">Primer Flo 56</th>
+    <td>1</td>
+    </tr>
+  <tr>
+    <th scope="row">Phusion</th>
+    <td>1</td>
+    </tr>
+  <tr>
+    <th scope="row">Phusion Buffer 5x</th>
+    <td>10</td>
+    </tr>
+  <tr>
+    <th scope="row">dNTP Mix</th>
+    <td>1</td>
+    </tr>
+  <tr>
+    <th scope="row">Water</th>
+    <td>35</td>
+    </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>50</td>
+  </tr>
+</table>
+	<br />
+       <table width="100%" border="1">
+  <tr>
+    <th scope="col">Step</th>
+    <th scope="col">Temperature &deg;C</th>
+    <th scope="col">Time</th>
+  </tr>
+  <tr>
+    <th scope="row">1</th>
+    <td>98</td>
+    <td>3 min</td>
+  </tr>
+  <tr>
+    <th scope="row">2</th>
+    <td>98</td>
+    <td>30 sec</td>
+  </tr>
+  <tr>
+    <th scope="row">3</th>
+    <td>55</td>
+    <td>1min 45sec</td>
+  </tr>
+  <tr>
+    <th scope="row">4</th>
+    <td>72</td>
+    <td>2 min</td>
+  </tr>
+  <tr>
+    <th scope="row">5</th>
+    <td>Go To 2</td>
+    <td>30x</td>
+  </tr>
+  <tr>
+    <th scope="row">6</th>
+    <td>72</td>
+    <td>4min</td>
+  </tr>
+  <tr>
+    <th scope="row">7</th>
+    <td>8</td>
+    <td>infinite</td>
+  </tr>
+</table>
+	<p>The fragments were analysed on an 1% agarose gel.</p>
+    <img src="https://static.igem.org/mediawiki/2014/c/ce/MR_2014-06-14_DarpinHag.jpg" width="20%" />
+    </div>
+</fieldset>
+<fieldset class="exp15">
+    <legend><a name="exp15.54">15.54 new PCR amplification of cup1-1</a></legend>
+    <div class="aim">
+    <p>Aim: amplification of cup1-1 domain for Gibson assembly into pMAD</p>
+    </div>
+    <div class="exp-content">
+    <p>The cup1-1 domain was amplified via PCR with new primers iGEM-024 and -025. The fragment should be ca. 160 bp.</p>
+        <table width="100%" border="1">
+  <tr>
+    <th scope="col">Mix</th>
+    <th scope="col">Volume</th>
+    </tr>
+  <tr>
+    <th scope="row">Template (cup1-1 gene)</th>
+    <td>1</td>
+    </tr>
+  <tr>
+    <th scope="row">Primer iGEM-024</th>
+    <td>1</td>
+    </tr>
+  <tr>
+    <th scope="row">Primer iGEM-025</th>
+    <td>1</td>
+    </tr>
+  <tr>
+    <th scope="row">Phusion</th>
+    <td>1</td>
+    </tr>
+  <tr>
+    <th scope="row">Phusion Buffer 5x</th>
+    <td>10</td>
+    </tr>
+  <tr>
+    <th scope="row">dNTP Mix</th>
+    <td>1</td>
+    </tr>
+  <tr>
+    <th scope="row">Water</th>
+    <td>35</td>
+    </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>50</td>
+  </tr>
+</table>
+	<br />
+       <table width="100%" border="1">
+  <tr>
+    <th scope="col">Step</th>
+    <th scope="col">Temperature &deg;C</th>
+    <th scope="col">Time</th>
+  </tr>
+  <tr>
+    <th scope="row">1</th>
+    <td>98</td>
+    <td>3 min</td>
+  </tr>
+  <tr>
+    <th scope="row">2</th>
+    <td>98</td>
+    <td>30 sec</td>
+  </tr>
+  <tr>
+    <th scope="row">3</th>
+    <td>55</td>
+    <td>30 sec</td>
+  </tr>
+  <tr>
+    <th scope="row">4</th>
+    <td>72</td>
+    <td>30 sec</td>
+  </tr>
+  <tr>
+    <th scope="row">5</th>
+    <td>Go To 2</td>
+    <td>30x</td>
+  </tr>
+  <tr>
+    <th scope="row">6</th>
+    <td>72</td>
+    <td>4min</td>
+  </tr>
+  <tr>
+    <th scope="row">7</th>
+    <td>8</td>
+    <td>infinite</td>
+  </tr>
+</table>
+	<img src="https://static.igem.org/mediawiki/2014/e/e2/MR_2014-06-14_cup1-1.jpg" width="10%" />
+	<p>Referring to the gel analysis the amplification was successful.</p>
+    </div>
+</fieldset>
+</div>
+<!-- 15.06.14 -->
+<div class="notebooky-entry">
+<h2 class="title">
+	<a name="15.06.2014">15.06.2014</a>
+</h2>
+<fieldset class="ex20">
+    <legend><a name="exp20.3a">20.3 Overnight culture of blue clones</a></legend>
+    <div class="aim">
+    <p>Aim: transformation of plasmid into Bacillus subtilis WT3610</p>
+    </div>
+    <div class="exp-content">
+    <p>Colonies  were grown on the plates with transformed piGEM-005 &amp; - 018. The blue/  white screening showed positive transformed blue clones.&nbsp; 3 clones of different morphology per plate  were picked and used for inoculation of LB-MLS (4 mL LB, 4 &micro;L Lincomycin, 4 &micro;L  Erythromycin). Incubation was carried out overnight at 30&deg;C with the 6  cultures.<strong> </strong></p>
+</div>
+</fieldset>
+</div>
+<!-- 17.06.14 -->
+<div class="notebooky-entry">
+<h2 class="title">
+	<a name="17.06.2014">17.06.2014</a>
+</h2>
+<fieldset class="exp20">
+    <legend><a name="exp20.3b">20.3 First temperature shift</a></legend>
+    <div class="aim">
+    <p>Aim: integration of  pMAD-Insert into Bacillus chromosome via flanks</p>
+    </div>
+    <div class="exp-content">
+    <p>The 6  overnight cultures were used to inoculate 10 mL LB MLS until&nbsp; the culture obtained an OD of 0,1. The  cultures were incubated at 30&deg;C for 2h.</p>
+    <p>Then  the temperature was shifted to 42&deg;C for 6h.</p>
+    <p>After  the heat shock dilutions from 10-4 to 10-6 of each culture  were plated out on MLS-X-Gal so that 18 plates could be incubated overnight at  42&deg;C.</p>
+</div>
+</fieldset>
+<fieldset class="exp15">
+    <legend><a name="exp15.54">15.54 Gibson-assebmly with  PCR amplificated cup1-1 and spe1 cut piGEM-005</a></legend>
+    <div class="aim">
+    <p>Aim: insertion of cup1-1 into piGEM-005</p>
+    </div>
+    <div class="exp-content">
+    <p>The cup1-1 domain was amplified via PCR with new primers iGEM-024 and  -025. Vector and template were diluted to a concentration under 75 ng/&micro;L. Spe1  cut piGEM-005 was used from the cloning experiments with DARPin.</p>
+    <p>PCR fragment cup1-1 (464 ng/&micro;L) dilution 1:10</p>
+    <p>Spe1 cut pIGEM-005 (148 ng/&micro;L) dilution 1:2</p>
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Component</th>
+    <th scope="col">Volume [&micro;l]</th>
+  </tr>
+  <tr>
+    <th scope="row">Gibson-Mix</th>
+    <td>15</td>
+  </tr>
+  <tr>
+    <th scope="row">Insert (cup1-1 58 ng/&micro;L)</th>
+    <td>1,3</td>
+  </tr>
+  <tr>
+    <th scope="row">piGEM-005 </th>
+    <td>1</td>
+  </tr>
+  <tr>
+    <th scope="row">Water</th>
+    <td>2,7</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>20</td>
+  </tr>
+</table>
+	<p>The mix was incubated 5 min at room temperature and then for 1h at 50&deg;C.</p>
+	<p>In the end the whole mix was transformed into E.Coli XL1-Blue and plated  out on LB-Amp. Incubation was done overnight at 37&deg;C.</p>
+</div>
+</fieldset>
+</div>
+<!-- 18.06.14 -->
+<div class="notebooky-entry">
+<h2 class="title">
+	<a name="18.06.2014">18.06.2014</a>
+</h2>
+<fieldset class="exp20">
+    <legend><a name="exp20.4">20.4 Second temperature shift</a></legend>
+    <div class="aim">
+    <p>Aim: flip out of the pMAD backbone</p>
+    </div>
+    <div class="exp-content">
+    <p>One  blue colony per diluted clone was used to inoculate 4 mL LB. The 6 cultures  were incubated at 30&deg;C for 6h and afterwards for 3h at 42&deg;C.</p>
+    <p>Dilutions  from 10-4&shy; to 10-6 were plated out on 18 X-Gal plates  WITHOUT MLS selection. The positive clones should not contain the resistance  inside the backbone as well as the galactosidase. The plates were incubated at  42&deg;C overnight.</p>
+</div>
+</fieldset>
+<fieldset class="exp15">
+    <legend><a name="exp15.54">15.54 Checking Gibson assembly plate piGEM-005-cup1-1</a></legend>
+    <div class="aim">
+    <p>Aim: insertion of cup1-1 into piGEM-005</p>
+    </div>
+    <div class="exp-content">
+    <p>Unfortunately the plate was empty, no colonies. The vector was cut newly in order to repeat the assembly.</p>
+    </div>
+</fieldset>
+<fieldset class="exp15">
+    <legend><a name="exp15.55">15.55 restriction digest of piGEM-005 with spe1</a></legend>
+    <div class="aim">
+    <p>Aim: linearizing plasmid for repeating the Gibson assembly</p>
+    </div>
+    <div class="exp-content">
+    <p>In order to repeat the Gibson assembly the piGEM-005 was cut with spe1 freshly.</p>
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Component</th>
+    <th scope="col">Volume [&micro;l]</th>
+  </tr>
+  <tr>
+    <th scope="row">piGEM-005 (108 ng/&micro;L)</th>
+    <td>10</td>
+  </tr>
+  <tr>
+    <th scope="row">Cutsmart 10x</th>
+    <td>2</td>
+  </tr>
+  <tr>
+    <th scope="row">Spe1</th>
+    <td>0,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Water</th>
+    <td>7,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>20</td>
+  </tr>
+</table>
+	<p>Incubation 1h  at 37&deg;C with following heat shock at 80&deg;C</p>
+</div>
+</fieldset>
+</div>
+<!-- 19.06.14 -->
+<div class="notebooky-entry">
+<h2 class="title">
+	<a name="19.06.2014">19.06.2014</a>
+</h2>
+<fieldset class="exp20">
+    <legend><a name="exp20.5">20.5 selection of positive clones</a></legend>
+    <div class="aim">
+    <p>Aim: checking the correct flip out of the pMAD backbone</p>
+    </div>
+    <div class="exp-content">
+    <p>From  the dilution plates was one WHITE clone picked and transferred on a Master  X-Gal Plate as well as on a MLS plate so that 18 clones were proven for the  right integration of the insert although flipping out the pMAD backbone.</p>
+    <p>The  plates were incubated at 42&deg;C overnight.</p>
+</div>
+</fieldset>
+<fieldset class="exp15">
+    <legend><a name="exp15.56">15.56 new Gibson-assembly with  cup1-1 and spe1 cut piGEM-005</a></legend>
+    <div class="aim">
+    <p>Aim: insertion of cup1-1 into piGEM-005</p>
+    </div>
+    <div class="exp-content">
+    <p>As insert cup1-1 PCR product from 15.55 and Spe1 cut piGEM-005 from  15.55 were used for a new Gibson assembly.</p>
+<p>PCR fragment cup1-1 (464 ng/&micro;L)</p>
+    <p>Spe1 cut pIGEM-005 (53 ng/&micro;L) </p>
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Component</th>
+    <th scope="col">Volume [&micro;l]</th>
+  </tr>
+  <tr>
+    <th scope="row">Gibson-Mix</th>
+    <td>15</td>
+  </tr>
+  <tr>
+    <th scope="row">Insert (cup1-1 58 ng/&micro;L)</th>
+    <td>2,5</td>
+  </tr>
+  <tr>
+    <th scope="row">piGEM-005 </th>
+    <td>2,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>20</td>
+  </tr>
+</table>
+	<p>The mix was incubated 5 min at room temperature and then for 1h at 50&deg;C.</p>
+<p>In the end the whole mix was transformed into E.Coli XL1-Blue and plated  out on LB-Amp. Incubation was done overnight at 37&deg;C.</p>
+</div>
+</fieldset>
+</div>
+<!-- 20.06.14 -->
+<div class="notebooky-entry">
+<h2 class="title">
+	<a name="20.06.2014">20.06.2014</a>
+</h2>
+<fieldset class="exp20">
+    <legend><a name="exp20.5">20.5 selection of positive clones</a></legend>
+    <div class="aim">
+    <p>Aim: checking the correct flip out of the pMAD backbone</p>
+    </div>
+    <div class="exp-content">
+    <p>The white colonies  grew on the X-Gal Master plates but not on MLS plates so the transformation  seemed to be successful. The Backbone with the MLS resistance flipped out of  the genome</p>
+    </div>
+</fieldset>
+<fieldset class="exp20">
+    <legend><a name="exp20.6">20. 6 cPCR with checked clones</a></legend>
+    <div class="aim">
+    <p>Aim: checking integration of constructs Hag-Spe and Hag-Spe-DARPin into B. s. genome</p>
+    </div>
+    <div class="exp-content">
+    <p>No  clone was growing on MLS plates so the picked clones seemed to be positive. In  order to check the correct integration of the domain constructs a cPCR with the  picked clones on the X-Gal plates was done. The picked 18 B.s. clones were  cooked in 10 &micro;L PBS for 5 min at 95&deg;C.</p>
+         <table width="100%" border="1">
+          <tr>
+            <th scope="col">Mix</th>
+            <th scope="col">Master-Mix for 18 attempts (&micro;L)</th>
+            <th scope="col">Mix for PCR attempt (&micro;L)</th>
+           </tr>
+          <tr>
+            <th scope="row">Colony (picked clones 1-9 from Flagellin/-DARPin B.s.  plates)</th>
+            <td>-</td>
+            <td>Part of a cooked colony</td>
+            </tr>
+          <tr>
+            <th scope="row">Primer Flo54 Hag-fw</th>
+            <td>9</td>
+            <td>-</td>
+            </tr>
+          <tr>
+            <th scope="row">Primer Flo56 Hag-rv</th>
+            <td>9</td>
+            <td>-</td>
+            </tr>
+          <tr>
+            <th scope="row">Phusion</th>
+            <td>18</td>
+            <td>-</td>
+            </tr>
+          <tr>
+            <th scope="row">Phusion Buffer 5x</th>
+            <td>72</td>
+            <td>-</td>
+            </tr>
+          <tr>
+            <th scope="row">dNTP Mix</th>
+            <td>9</td>
+            <td>-</td>
+            </tr>
+          <tr>
+            <th scope="row">Water</th>
+            <td>237</td>
+            <td>-</td>
+            </tr>
+          <tr>
+            <th scope="row">DMSO</th>
+            <td>6</td>
+            <td>-</td>
+            </tr>
+          <tr>
+            <th scope="row">Mastermix</th>
+            <td>-</td>
+            <td>20</td>
+            </tr>
+          <tr>
+            <th scope="row">Total Volume</th>
+            <td>100</td>
+            <td>360</td>
+          </tr>
+        </table>
+            <br />
+               <table width="100%" border="1">
+          <tr>
+            <th scope="col">Step</th>
+            <th scope="col">Temperature &deg;C</th>
+            <th scope="col">Time</th>
+          </tr>
+          <tr>
+            <th scope="row">1</th>
+            <td>98</td>
+            <td>3 min</td>
+          </tr>
+          <tr>
+            <th scope="row">2</th>
+            <td>98</td>
+            <td>30 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">3</th>
+            <td>55</td>
+            <td>1 min 45 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">4</th>
+            <td>72</td>
+            <td>2 min</td>
+          </tr>
+          <tr>
+            <th scope="row">5</th>
+            <td>Go To 2</td>
+            <td>30x</td>
+          </tr>
+          <tr>
+            <th scope="row">6</th>
+            <td>72</td>
+            <td>4min</td>
+          </tr>
+          <tr>
+            <th scope="row">7</th>
+            <td>8</td>
+            <td>infinite</td>
+          </tr>
+        </table>
+	<p>The gel showed no bands. The PCR had to be repeated.</p>
+	</div>
+</fieldset>
+<fieldset class="exp15">
+    <legend><a name="exp15.57">15.57 Miniprep of clones from Gibson assembly from 15.56</a></legend>
+    <div class="aim">
+    <p>Aim: Plasmid amplification for further experiments</p>
+    </div>
+    <div class="exp-content">
+    <p>4x 5 mL of LB-Amp was were  inoculated with a picked colony from a transformation plate with XL1-Blue  containing the Gibson-Assembly product from 15.56.</p>
+    <p>Incubation at 37&deg;C overnight.</p>
+</div>
+</fieldset>
+</div>
+<!-- 21.06.14 -->
+<div class="notebooky-entry">
+<h2 class="title">
+	<a name="21.06.2014">21.06.2014</a>
+</h2>
+<fieldset class="exp15">
+    <legend><a name="exp15.58">15.58 cPCR with colonies from Gibson piGEM-005 + cup1-1 plate</a></legend>
+    <div class="aim">
+    <p>Aim: checking correct insertion of cup1-1</p>
+    </div>
+    <div class="exp-content">
+    <p>In order to check the correct  insertion of the cup1-1 domain into the Hag-Flank-construct in pMAD a cPCR with  primers iGEM-025 (Cup1-1 rv) and Flo89 (pMAD-flank1-Bamh1 fw) was performed. The picked colonies were the same which wre  used to inoculate minipreps from 15.57. The fragment was supposed to e ca. 1250  bp. </p>
+    <table width="100%" border="1">
+          <tr>
+            <th scope="col">Mix</th>
+            <th scope="col"><strong>Master-Mix for 5 attempts (&micro;L)</strong></th>
+            <th scope="col"><strong>Mix for PCR attempt (&micro;L)</strong></th>
+            </tr>
+          <tr>
+            <th scope="row">Colony (picked clones 1-4 for miniprep)</th>
+            <td>-</td>
+            <td>Part of a  colony</td>
+        </tr>
+          <tr>
+            <th scope="row">Primer Flo89 </th>
+            <td>2,5</td>
+            <td>-</td>
+        </tr>
+          <tr>
+            <th scope="row">Primer piGEM-025</th>
+            <td>2,5</td>
+            <td>-</td>
+        </tr>
+          <tr>
+            <th scope="row">Phusion</th>
+            <td>2,5</td>
+            <td>-</td>
+            </tr>
+          <tr>
+            <th scope="row">Phusion Buffer 5x</th>
+            <td>20</td>
+            <td>-</td>
+            </tr>
+          <tr>
+            <th scope="row">dNTP Mix</th>
+            <td>2,5</td>
+            <td>-</td>
+            </tr>
+          <tr>
+            <th scope="row">Water</th>
+            <td>70</td>
+            <td>-</td>
+            </tr>
+          <tr>
+            <th scope="row">Mastermix</th>
+            <td>-</td>
+            <td>20</td>
+            </tr>
+          <tr>
+            <th scope="row">Total Volume</th>
+            <td>100</td>
+            <td>20</td>
+          </tr>
+        </table>
+            <br />
+          <table width="100%" border="1">
+          <tr>
+            <th scope="col">Step</th>
+            <th scope="col">Temperature &deg;C</th>
+            <th scope="col">Time</th>
+          </tr>
+          <tr>
+            <th scope="row">1</th>
+            <td>98</td>
+            <td>3 min</td>
+          </tr>
+          <tr>
+            <th scope="row">2</th>
+            <td>98</td>
+            <td>30 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">3</th>
+            <td>55</td>
+            <td>30 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">4</th>
+            <td>72</td>
+            <td>1 min 30 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">5</th>
+            <td>Go To 2</td>
+            <td>30x</td>
+          </tr>
+          <tr>
+            <th scope="row">6</th>
+            <td>72</td>
+            <td>4min</td>
+          </tr>
+          <tr>
+            <th scope="row">7</th>
+            <td>8</td>
+            <td>infinite</td>
+          </tr>
+        </table>
+        <p>The analysis via 1% agarose gel eletrophoresis showed now bands. All 4 picked clones were prepped to use the plasmid as template.</p>
+	</div>
+</fieldset>
+<fieldset class="exp15">
+    <legend><a name="exp15.59">15.59 PCR with prepped plasmid from Gibson piGEM-005 + cup1-1 plate</a></legend>
+    <div class="aim">
+    <p>Aim: checking correct insertion of cup1-1</p>
+    </div>
+    <div class="exp-content">
+    <p>This  time the prepped plasmid DNA from the picked 6clones was used as a template  with different primer pairs. First of all tie PCR attempts were performed with  primers Flo89 and Flo90 in order to receive the whole Hag-Flank-Cup1-1  construct with ca. 2100 bp length. As negative control also piGEM-005 was used  as template producing a 2000kb fragment. Because of the small difference all 6  attempts were also driven with the primers Flo89 and iGEM-025 (cup1-1 rv) in  order to check the insertion of cup1-1 directly with a fragment of 1268 bp.</p>
+    <table width="100%" border="1">
+      <tr>
+        <th scope="col">Mix</th>
+        <th scope="col"><strong>Master-Mix 1 for&nbsp;  5 attempts (&micro;L)</strong></th>
+        <th scope="col"><strong>Master-Mix 2 for&nbsp;  5 attempts (&micro;L)</strong></th>
+        <th scope="col"><strong>Mix 1 for PCR attempt (&micro;L)</strong></th>
+        <th scope="col"><strong>Mix 2for PCR attempt (&micro;L)</strong></th>
+      </tr>
+      <tr>
+        <th scope="row">Plasmid DNA from clone 1-4/ piGEM-005</th>
+        <td>-</td>
+        <td>-</td>
+        <td>1</td>
+        <td>-</td>
+      </tr>
+      <tr>
+        <th scope="row">Primer Flo89 </th>
+        <td>2,5</td>
+        <td>2,5</td>
+        <td>-</td>
+        <td>-</td>
+      </tr>
+      <tr>
+        <th scope="row">Primer Flo90</th>
+        <td>2,5</td>
+        <td>-</td>
+        <td>-</td>
+        <td>-</td>
+      </tr>
+      <tr>
+        <th scope="row">Primer piGEM-025</th>
+        <td>-</td>
+        <td>2,5</td>
+        <td>-</td>
+        <td>-</td>
+      </tr>
+      <tr>
+        <th scope="row">Phusion</th>
+        <td>2,5</td>
+        <td>2,5</td>
+        <td>-</td>
+        <td>-</td>
+      </tr>
+      <tr>
+        <th scope="row">Phusion Buffer 5x</th>
+        <td>20</td>
+        <td>20</td>
+        <td>-</td>
+        <td>-</td>
+      </tr>
+      <tr>
+        <th scope="row">dNTP-mix</th>
+        <td>2,5</td>
+        <td>2,5</td>
+        <td>-</td>
+        <td>-</td>
+      </tr>
+      <tr>
+        <th scope="row">Water</th>
+        <td>70</td>
+        <td>70</td>
+        <td>-</td>
+        <td>-</td>
+      </tr>
+      <tr>
+        <th scope="row">Master-Mix 1/ 2</th>
+        <td>-</td>
+        <td>-</td>
+        <td>20</td>
+        <td>20</td>
+      </tr>
+      <tr>
+        <th scope="row">Total Volume</th>
+        <td>100</td>
+        <td>100</td>
+        <td>20</td>
+        <td>20</td>
+      </tr>
+    </table>
+	<br />
+              <table width="100%" border="1">
+          <tr>
+            <th scope="col">Step</th>
+            <th scope="col">Temperature &deg;C</th>
+            <th scope="col">Time</th>
+          </tr>
+          <tr>
+            <th scope="row">1</th>
+            <td>98</td>
+            <td>3 min</td>
+          </tr>
+          <tr>
+            <th scope="row">2</th>
+            <td>98</td>
+            <td>30 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">3</th>
+            <td>55</td>
+            <td>30 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">4</th>
+            <td>72</td>
+            <td>20 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">5</th>
+            <td>Go To 2</td>
+            <td>30x</td>
+          </tr>
+          <tr>
+            <th scope="row">6</th>
+            <td>72</td>
+            <td>4min</td>
+          </tr>
+          <tr>
+            <th scope="row">7</th>
+            <td>8</td>
+            <td>infinite</td>
+          </tr>
+        </table>
+        <br />
+        <img src="https://static.igem.org/mediawiki/2014/6/61/MR_2014-06-21_piGEM-005_cup1-1.jpg" width="20%" />
+        <p>The gel analysis shows that all 4 clones seem to be positive. By amplification of the cup1-1 fragment with the plasmid DNA as template could proof that.</p>
+</div>
+</fieldset>
+<fieldset class="exp20">
+    <legend><a name="exp20.6a">20. 6 repeating cPCR with checked clones</a></legend>
+    <div class="aim">
+    <p>Aim: checking integration of constructs Hag-Spe and Hag-Spe-DARPin into B. s. genome</p>
+    </div>
+    <div class="exp-content">
+    <p>Because  of the unsuccessful cPCR before the PCR was repeated. The picked 18 B.s. clones  were cooked in 30 &micro;L PBS for 10 min at 95&deg;C.</p>
+            <table width="100%" border="1">
+          <tr>
+            <th scope="col">Mix</th>
+            <th scope="col">Master-Mix for 18 attempts (&micro;L)</th>
+            <th scope="col">Mix for PCR attempt (&micro;L)</th>
+           </tr>
+          <tr>
+            <th scope="row">Colony (picked clones 1-9 from Flagellin/-DARPin B.s.  plates)</th>
+            <td>-</td>
+            <td>Part of a cooked colony</td>
+            </tr>
+          <tr>
+            <th scope="row">Primer Flo54 Hag-fw</th>
+            <td>9</td>
+            <td>-</td>
+            </tr>
+          <tr>
+            <th scope="row">Primer Flo56 Hag-rv</th>
+            <td>9</td>
+            <td>-</td>
+            </tr>
+          <tr>
+            <th scope="row">Phusion</th>
+            <td>18</td>
+            <td>-</td>
+            </tr>
+          <tr>
+            <th scope="row">Phusion Buffer 5x</th>
+            <td>72</td>
+            <td>-</td>
+            </tr>
+          <tr>
+            <th scope="row">dNTP Mix</th>
+            <td>9</td>
+            <td>-</td>
+            </tr>
+          <tr>
+            <th scope="row">Water</th>
+            <td>237</td>
+            <td>-</td>
+            </tr>
+          <tr>
+            <th scope="row">DMSO</th>
+            <td>6</td>
+            <td>-</td>
+            </tr>
+          <tr>
+            <th scope="row">Mastermix</th>
+            <td>-</td>
+            <td>20</td>
+            </tr>
+          <tr>
+            <th scope="row">Total Volume</th>
+            <td>100</td>
+            <td>360</td>
+          </tr>
+        </table>
+            <br />
+               <table width="100%" border="1">
+          <tr>
+            <th scope="col">Step</th>
+            <th scope="col">Temperature &deg;C</th>
+            <th scope="col">Time</th>
+          </tr>
+          <tr>
+            <th scope="row">1</th>
+            <td>98</td>
+            <td>3 min</td>
+          </tr>
+          <tr>
+            <th scope="row">2</th>
+            <td>98</td>
+            <td>30 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">3</th>
+            <td>55</td>
+            <td>1 min 45 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">4</th>
+            <td>72</td>
+            <td>2 min</td>
+          </tr>
+          <tr>
+            <th scope="row">5</th>
+            <td>Go To 2</td>
+            <td>30x</td>
+          </tr>
+          <tr>
+            <th scope="row">6</th>
+            <td>72</td>
+            <td>4min</td>
+          </tr>
+          <tr>
+            <th scope="row">7</th>
+            <td>8</td>
+            <td>infinite</td>
+          </tr>
+        </table>
+        <br />
+        <img src="https://static.igem.org/mediawiki/2014/1/18/MR_2014-06-21_darpin.jpg" width="30%" />
+</div>
+</fieldset>
+<fieldset class="exp20">
+    <legend><a name="exp20.6b">20. 6 repeating cPCR with checked clones</a></legend>
+    <div class="exp-content">
+    <p>The clones with piGEM-005 seem to be positive all 9. Clone 1, 3, 7, 8 and  9 of transformed piGEM-018.1 might be positive as well as clone 2-6 from  piGEM-018.2. The sequencing of the PCR products should tell us if the insertion  was successful.</p>
+</div>
+</fieldset>
+</div>
+<!-- 22.06.14 -->
+<div class="notebooky-entry">
+<h2 class="title">
+	<a name="22.06.2014">22.06.2014</a>
+</h2>
+<fieldset class="exp18">
+    <legend><a name="exp18.31">18.31 PCR amplification of DARPin-Hag and Hag fragment</a></legend>
+    <div class="aim">
+    <p>Aim: amplification of DARPin-Hag fragments for repeating the ligation </p>
+    </div>
+    <div class="exp-content">
+    <p>piGEM-018  &amp; -005 were used as template for a PCR with the primers from Florian  Altegoer 54 and 56. The products could be used for further cloning after  Nco/Bam digest. </p>
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Content</th>
+    <th scope="col">Volume [&micro;l]</th>
+  </tr>
+  <tr>
+    <th scope="row">Template (piGEM-005 &amp; -018)</th>
+    <td>1</td>
+  </tr>
+  <tr>
+    <th scope="row">Primer Flo 54 </th>
+    <td>1</td>
+  </tr>
+  <tr>
+    <th scope="row">Primer Flo 56</th>
+    <td>1</td>
+  </tr>
+  <tr>
+    <th scope="row">Phusion</th>
+    <td>1</td>
+  </tr>
+  <tr>
+    <th scope="row">Phusion Buffer 5x</th>
+    <td>10</td>
+  </tr>
+  <tr>
+    <th scope="row">dNTP Mix</th>
+    <td>1</td>
+  </tr>
+  <tr>
+    <th scope="row">Water</th>
+    <td>35</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>50</td>
+  </tr>
+</table>
+	<br />
+                   <table width="100%" border="1">
+          <tr>
+            <th scope="col">Step</th>
+            <th scope="col">Temperature &deg;C</th>
+            <th scope="col">Time</th>
+          </tr>
+          <tr>
+            <th scope="row">1</th>
+            <td>98</td>
+            <td>3 min</td>
+          </tr>
+          <tr>
+            <th scope="row">2</th>
+            <td>98</td>
+            <td>30 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">3</th>
+            <td>55</td>
+            <td>30 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">4</th>
+            <td>72</td>
+            <td>1 min 45 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">5</th>
+            <td>Go To 2</td>
+            <td>30x</td>
+          </tr>
+          <tr>
+            <th scope="row">6</th>
+            <td>72</td>
+            <td>4min</td>
+          </tr>
+          <tr>
+            <th scope="row">7</th>
+            <td>8</td>
+            <td>infinite</td>
+          </tr>
+        </table>
+</div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.32">18.32 cPCR with new clones</a></legend>
+    <div class="aim">
+    <p>Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pet24d</p>
+    </div>
+    <div class="exp-content">
+    <p>more clones from each  plate were picked to analyse them via cPCR with the primers flo54 and flo56  (Hag-fw and Hag-rv). The result should be a ca. 1kb fragment for correct  pet24d-Hag containing clones and a 1,5 kb fragment for pet24d-Hag-DARPin  containing clones.</p>
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Content</th>
+    <th scope="col">Volume (&micro;L)</th>
+    <th scope="col">MM for 14 attempts (&micro;L</th>
+  </tr>
+  <tr>
+    <th scope="row"><p>Colony</p>
+&nbsp;(8-15 from pet-Hag,7-14 from pet-Hag-DARPin)</th>
+    <td>1 colony</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Primer Flo 54 </th>
+    <td>-</td>
+    <td>7</td>
+  </tr>
+  <tr>
+    <th scope="row">Primer Flo 56</th>
+    <td>-</td>
+    <td>7</td>
+  </tr>
+  <tr>
+    <th scope="row">Phusion</th>
+    <td>-</td>
+    <td>7</td>
+  </tr>
+  <tr>
+    <th scope="row">Phusion Buffer 5x</th>
+    <td>-</td>
+    <td>56</td>
+  </tr>
+  <tr>
+    <th scope="row">dNTP Mix</th>
+    <td>-</td>
+    <td>7</td>
+  </tr>
+  <tr>
+    <th scope="row">Water</th>
+    <td>-</td>
+    <td>196</td>
+  </tr>
+  <tr>
+    <th scope="row">Mastermix</th>
+    <td>20</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>20</td>
+    <td>280</td>
+  </tr>
+</table>
+	<br />
+         <table width="100%" border="1">
+          <tr>
+            <th scope="col">Step</th>
+            <th scope="col">Temperature &deg;C</th>
+            <th scope="col">Time</th>
+          </tr>
+          <tr>
+            <th scope="row">1</th>
+            <td>98</td>
+            <td>3 min</td>
+          </tr>
+          <tr>
+            <th scope="row">2</th>
+            <td>98</td>
+            <td>30 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">3</th>
+            <td>55</td>
+            <td>30 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">4</th>
+            <td>72</td>
+            <td>1 min 45 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">5</th>
+            <td>Go To 2</td>
+            <td>30x</td>
+          </tr>
+          <tr>
+            <th scope="row">6</th>
+            <td>72</td>
+            <td>4min</td>
+          </tr>
+          <tr>
+            <th scope="row">7</th>
+            <td>8</td>
+            <td>infinite</td>
+          </tr>
+        </table>
+    </div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.33">18.33 pet24d digest with Nco/Bam</a></legend>
+    <div class="aim">
+    <p>Aim: preparing vector for new ligation attempts</p>
+    </div>
+    <div class="exp-content">
+    <p>Because  of the low amount of right clones new vector (pet24d) was cut with Nco1 and  BamH1 according to the following scheme:</p>
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Component</th>
+    <th scope="col"><strong><u>Volume (&micro;L)</u></strong></th>
+  </tr>
+  <tr>
+    <th scope="row">Pet24d (50 ng/&micro;L)</th>
+    <td>20</td>
+  </tr>
+  <tr>
+    <th scope="row">Cutsmart 10x</th>
+    <td>3</td>
+  </tr>
+  <tr>
+    <th scope="row">Nco1</th>
+    <td>0,5</td>
+  </tr>
+  <tr>
+    <th scope="row">BamH1</th>
+    <td>0,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Water</th>
+    <td>6</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>30</td>
+  </tr>
+</table>
+	<p>Incubation at 37°C for 2h with heat shock in the end at 80&deg;C</p>
+	<p>Endconcentration:  32 ng/&micro;L</p>
+</div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.34">18.34 restriction digest of Hag PCR fragments from 18.31 with Nco1/ BamH1</a></legend>
+    <div class="aim">
+    <p>Aim: creating restriction sites for cloning into pet24d cut with Nco/Bam</p>
+    </div>
+    <div class="exp-content">
+    <p>The PCR products from 18.x were digested with Nco1 and BamH1 to create restriction sites in order to ligate the fragments into Nco/Bam cut pet24d in case of negative clones refering to the cPCR from 18.x</p>
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Component</th>
+    <th scope="col">PCR Hag-fragment (&micro;L)</th>
+    <th scope="col">PCR Hag-DARPin fragment  (&micro;L)</th>
+  </tr>
+  <tr>
+    <th scope="row">PCR products</th>
+    <td>45</td>
+    <td>45</td>
+  </tr>
+  <tr>
+    <th scope="row">Cutsmart 10x</th>
+    <td>5,2</td>
+    <td>5,2</td>
+  </tr>
+  <tr>
+    <th scope="row">Nco1</th>
+    <td>0,5</td>
+    <td>0,5</td>
+  </tr>
+  <tr>
+    <th scope="row">BamH1</th>
+    <td>0,5</td>
+    <td>0,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Water</th>
+    <td>3,8</td>
+    <td>3,8</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>52</td>
+    <td>52</td>
+  </tr>
+</table>
+	<p>Incubation  for 2h at 37&deg;C with heat shock at 80&deg;C.</p>
+	<p>Endconcentration: <br />
+	  digested Hag-fragment  260 ng/&micro;L	<br />
+	  digested  Hag-fragment 268 ng/&micro;L</p>
+    <p> </p>
+    </div>
+</fieldset>
+<fieldset class="exp15">
+    <legend><a name="exp15.60">15.60 PCR pMAD-Hag-Flank-cup1-1 (piGEM-016)</a></legend>
+    <div class="aim">
+    <p>Aim: checking success of Gibson assembly with pMAD-Hag-Flank and cup1-1</p>
+    </div>
+    <div class="exp-content">
+    <p>Using  the plasmids as template the cup1-1 fragment at 160 bp should be visible on the  agarose gel. As positive control PCR products from the cup1-1 amplification  used for the Gibson Assembly into piGEM-005 were applicated on the gel as well. </p>
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Content</th>
+    <th scope="col">Volume (&micro;L)</th>
+    <th scope="col">MM for 5 attempts (&micro;L)</th>
+  </tr>
+  <tr>
+    <th scope="row">Template (Plasmid from clone 1-4)</th>
+    <td>0,5</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Primer iGEM-024</th>
+    <td>-</td>
+    <td>2,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Primer iGEM-025</th>
+    <td>-</td>
+    <td>2,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Phusion</th>
+    <td>-</td>
+    <td>2,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Phusion Buffer 5x</th>
+    <td>-</td>
+    <td>20</td>
+  </tr>
+  <tr>
+    <th scope="row">dNTP Mix</th>
+    <td>-</td>
+    <td>2,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Water</th>
+    <td>-</td>
+    <td>70</td>
+  </tr>
+  <tr>
+    <th scope="row">Mastermix</th>
+    <td>19,5</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>20</td>
+    <td>100</td>
+  </tr>
+</table>
+	<br />
+    <table width="100%" border="1">
+          <tr>
+            <th scope="col">Step</th>
+            <th scope="col">Temperature &deg;C</th>
+            <th scope="col">Time</th>
+          </tr>
+          <tr>
+            <th scope="row">1</th>
+            <td>98</td>
+            <td>3 min</td>
+          </tr>
+          <tr>
+            <th scope="row">2</th>
+            <td>98</td>
+            <td>30 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">3</th>
+            <td>55</td>
+            <td>30 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">4</th>
+            <td>72</td>
+            <td>20 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">5</th>
+            <td>Go To 2</td>
+            <td>30x</td>
+          </tr>
+          <tr>
+            <th scope="row">6</th>
+            <td>72</td>
+            <td>4min</td>
+          </tr>
+          <tr>
+            <th scope="row">7</th>
+            <td>8</td>
+            <td>infinite</td>
+          </tr>
+        </table>
+        <br />
+        <img src="https://static.igem.org/mediawiki/2014/0/02/MR_2014-06-22_15.60.jpg" width="30%" />
+        <p>The bands under the 200 bp mark indicate the positive insertion of  cup1-1 into piGEM-005. The plasmid has to be sequenced and is named iGEM-016.</p>
+</div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.35">18.35 test digest with Nco/Bam – Checking insertion of Hag/-DARPin into pet24d</a></legend>
+    <div class="aim">
+    <p>Aim: proving insertion of Hag/-DARPin fragment into pet24d</p>
+    </div>
+    <div class="exp-content">
+    <p>The  plasmids are digested with Nco1 and BamH1. In case of a correct insertion the  pet24d backbone and the insert should be seen on the gel at 5300 bp and 1000/  1500 bp. As control Pet24d-Hag-Flank (piGEM-001) is used to check the  mastermix.</p>
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Component</th>
+    <th scope="col">Volume (&micro;l)</th>
+    <th scope="col">Mastermix</th>
+  </tr>
+  <tr>
+    <th scope="row">2x Plasmid from clone 6</th>
+    <td>5</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Cutsmart 10x</th>
+    <td>-</td>
+    <td>5</td>
+  </tr>
+  <tr>
+    <th scope="row">Nco1</th>
+    <td>-</td>
+    <td>0,5</td>
+  </tr>
+  <tr>
+    <th scope="row">BamH1</th>
+    <td>-</td>
+    <td>0,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Water</th>
+    <td>-</td>
+    <td>19</td>
+  </tr>
+  <tr>
+    <th scope="row"><strong>Total</strong> Volume</th>
+    <td>10</td>
+    <td>25</td>
+  </tr>
+</table>
+</div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.36">18.36 ligation of pet24d  and PCR Hag/ Hag-DARPin fragments cut Nco/Bam</a></legend>
+    <div class="aim">
+    <p>Aim: ligation of construct with pet24d for overproduction of flagellin and crystallization</p>
+    </div>
+    <div class="exp-content">
+    <p>The  Nco/cut Flagellin PCR products from 18.x (from clone 7 and piGEM-005) were  ligated with Nco1 and BamH1 cut pet24d. </p>
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Component</th>
+    <th scope="col">Pet-Hag attempt (&micro;L) </th>
+    <th scope="col">Pet-Hag-DARPin attempt (&micro;L)</th>
+  </tr>
+  <tr>
+    <th scope="row">Insert (PCR fragments) (ca. 260 ng/&micro;L)</th>
+    <td>2</td>
+    <td>2</td>
+  </tr>
+  <tr>
+    <th scope="row">Vector (pet24d, c= 50ng/&micro;L)</th>
+    <td>5</td>
+    <td>5</td>
+  </tr>
+  <tr>
+    <th scope="row">Ligase-Buffer 10x</th>
+    <td>2</td>
+    <td>2</td>
+  </tr>
+  <tr>
+    <th scope="row">T4 Ligase</th>
+    <td>1</td>
+    <td>10</td>
+  </tr>
+  <tr>
+    <th scope="row">Milipore Water</th>
+    <td>10</td>
+    <td>10</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>20</td>
+    <td>20</td>
+  </tr>
+</table>
+	<p>The attempts were carried out in double and incubated at room  temperature -One attempt for 1h&nbsp; followed  by transformation into <em>E.Coli XL1-Blue </em>and  the second one overnight.</p>
+</div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.37a">18.37 repetition of PCR with 3 clones of Pet-Hag and Pet-Hag-DARPin ligation</a></legend>
+    <div clacc="aim">
+    <p>Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pet24d</p>
+    </div>
+    <div class="exp-content">
+    <p>3  clones from ligation plates with pet-Hag and pet-Hag-DARPin were resuspended in  30 &micro;L PBS and cooked at 95 &deg;C for 10min. After that procedure 1 &micro;L of this  suspenion was used as PCR template.</p>
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Content</th>
+    <th scope="col">Volume (&micro;L)</th>
+    <th scope="col">MM for 7 attempts (&micro;L)</th>
+  </tr>
+  <tr>
+    <th scope="row">Template ( 1&micro;L cooked suspension)<br />
+&nbsp;(8-10 from pet-Hag, 7-9 from pet-Hag-DARPin)</th>
+    <td>1</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Primer Flo 54 </th>
+    <td>-</td>
+    <td>3,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Primer Flo 56</th>
+    <td>-</td>
+    <td>3,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Phusion</th>
+    <td>-</td>
+    <td>3,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Phusion Buffer 5x</th>
+    <td>-</td>
+    <td>28</td>
+  </tr>
+  <tr>
+    <th scope="row">dNTP-mix</th>
+    <td>-</td>
+    <td>3,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Water</th>
+    <td>-</td>
+    <td>98</td>
+  </tr>
+  <tr>
+    <th scope="row">Mastermix</th>
+    <td>19</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>20</td>
+    <td>140</td>
+  </tr>
+</table>
+	<br />
+            <table width="100%" border="1">
+          <tr>
+            <th scope="col">Step</th>
+            <th scope="col">Temperature &deg;C</th>
+            <th scope="col">Time</th>
+          </tr>
+          <tr>
+            <th scope="row">1</th>
+            <td>98</td>
+            <td>3 min</td>
+          </tr>
+          <tr>
+            <th scope="row">2</th>
+            <td>98</td>
+            <td>30 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">3</th>
+            <td>55</td>
+            <td>30 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">4</th>
+            <td>72</td>
+            <td>1 min 45 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">5</th>
+            <td>Go To 2</td>
+            <td>30x</td>
+          </tr>
+          <tr>
+            <th scope="row">6</th>
+            <td>72</td>
+            <td>4min</td>
+          </tr>
+          <tr>
+            <th scope="row">7</th>
+            <td>8</td>
+            <td>infinite</td>
+          </tr>
+        </table>
+        <p>Run overnight</p>
+</div>
+</fieldset>
+<fieldset class="exp">
+    <legend><a name="exp_1">Transformation</a></legend>
+    <div class="exp-content">
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Plasmid</th>
+    <th scope="col">Concentration (ng/&micro;L)</th>
+    <th scope="col">Antibiotic</th>
+    <th scope="col">Cells</th>
+    <th scope="col">Volume (&micro;L)</th>
+  </tr>
+  <tr>
+    <th scope="row">Pet24d</th>
+    <td>148</td>
+    <td>Can</td>
+    <td>DH5&alpha;</td>
+    <td>1</td>
+  </tr>
+  <tr>
+    <th scope="row">piGEM-018</th>
+    <td>160</td>
+    <td>Amp</td>
+    <td>DH5&alpha;</td>
+    <td>0,5</td>
+  </tr>
+  <tr>
+    <th scope="row">piGEM-014</th>
+    <td>350</td>
+    <td>Amp</td>
+    <td>DH5&alpha;</td>
+    <td>0,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Gibson pMAD-cup1-1 clone 4</th>
+    <td>60</td>
+    <td>Amp</td>
+    <td>DH5&alpha;</td>
+    <td>1</td>
+  </tr>
+  <tr>
+    <th scope="row">Pet-Hag attempt from 18.36</th>
+    <td>-</td>
+    <td>Can</td>
+    <td>XL1-Blue</td>
+    <td>20</td>
+  </tr>
+  <tr>
+    <th scope="row">Pet-Hag-DARPin attempt from 18.36</th>
+    <td>-</td>
+    <td>Can</td>
+    <td>XL1-Blue</td>
+    <td>20</td>
+  </tr>
+  <tr>
+    <th scope="row">Control pet24d cut Nco/Bam</th>
+    <td>32</td>
+    <td>Can</td>
+    <td>XL1-Blue</td>
+    <td>1</td>
+  </tr>
+</table>
+    </div>
+</fieldset>
+</div>
+<!-- 23.06.14 -->
+<div class="notebooky-entry">
+<h2 class="title">
+	<a name="23.06.2014">23.06.2014</a>
+</h2>
+<fieldset class="exp">
+    <legend><a name="exp_2">Sequencing of constructs from 23.06.2014</a></legend>
+    <div class="exp-content">
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Premix</th>
+    <th scope="col">Label-Nr.</th>
+    <th scope="col">Construct</th>
+    <th scope="col">Primer</th>
+  </tr>
+  <tr>
+    <th scope="row">1</th>
+    <td>AGB0023<strong>402</strong></td>
+    <td>piGEM-018  (pMAD-DARPin)</td>
+    <td>Flo54 (Hag-F-Nco)</td>
+  </tr>
+  <tr>
+    <th scope="row">2</th>
+    <td>AGB0023<strong>403</strong></td>
+    <td>piGEM-018  (pMAD-DARPin)</td>
+    <td>Flo56 (Hag-R-Bam)</td>
+  </tr>
+  <tr>
+    <th scope="row">3</th>
+    <td>AGB0023<strong>404</strong></td>
+    <td>pMAD-Hag-Flank-cup1-1</td>
+    <td>Flo54 (Hag-F-Nco)</td>
+  </tr>
+  <tr>
+    <th scope="row">4</th>
+    <td>AGB0023<strong>405</strong></td>
+    <td>pMAD-Hag-Flank-cup1-1</td>
+    <td>Flo56 (Hag-R-Bam)</td>
+  </tr>
+  <tr>
+    <th scope="row">5</th>
+    <td>AGB0023<strong>406</strong></td>
+    <td>piGEM-002 (Nose  plasmid)</td>
+    <td>TW259</td>
+  </tr>
+</table>
+    </div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.37b">18.37 repetition of PCR with 3 clones of Pet-Hag and Pet-Hag-DARPin ligation</a></legend>
+    <div class="aim">
+    <p>Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pet24d</p>
+    </div>
+    <div class="exp-content">
+    <p>Gel electrophoresis:</p>
+    <img src="https://static.igem.org/mediawiki/2014/8/80/MR_2014-06-23_18.37.jpg" width="30%" />
+    <p>The gel shows negative bands in case of the Hag-DARPin clones. The PCR for Hag 8 and 9 did not work although we cooked the clones with PBS. The transformation efficiency seemed to be very low so clones from the new ligation attempts should be analysed.</p>
+    </div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.38">18.38 ligation checking success of transformed ligation attempts</a></legend>
+    <div class="exp-content">
+    <p>On every plate grew a high amount of colonies. 6 clones of each plate were picked for inoculation of minipreps and for cPCR after cooking with PBS. The clones were transferred to another LB-Can plate.</p>
+    </div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.39">18.39 cPCR with picked clones from 18.38 ligation attempt transformation</a></legend>
+    <div class="aim">
+    <p>Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pet24d</p>
+    </div>
+    <div class="exp-content">
+    <p>For  checking the insertion of the Hag/-DARPin into pet24 the clones from the  transformation plate were transferred to another LB-Can plate&nbsp; and cooked for 10 min in 30&micro;L PBS at 95&deg;C. At  the same time the colonies were used to inoculate LB-Can for minipreps.</p>
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Content</th>
+    <th scope="col">Volume (&micro;L)</th>
+    <th scope="col">MM for 14 attempts (&micro;L)</th>
+  </tr>
+  <tr>
+    <th scope="row">Template ( 1&micro;L cooked suspension)<br />
+&nbsp;(1-6 from pet-Hag, 1-6 from pet-Hag-DARPin)</th>
+    <td>1</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Primer Flo 54 </th>
+    <td>-</td>
+    <td>7</td>
+  </tr>
+  <tr>
+    <th scope="row">Primer Flo 56</th>
+    <td>-</td>
+    <td>7</td>
+  </tr>
+  <tr>
+    <th scope="row">Phusion</th>
+    <td>-</td>
+    <td>7</td>
+  </tr>
+  <tr>
+    <th scope="row">Phusion Buffer 5x</th>
+    <td>-</td>
+    <td>198</td>
+  </tr>
+  <tr>
+    <th scope="row">dNTP-mix</th>
+    <td>-</td>
+    <td>7</td>
+  </tr>
+  <tr>
+    <th scope="row">Water</th>
+    <td>-</td>
+    <td>98</td>
+  </tr>
+  <tr>
+    <th scope="row">Mastermix</th>
+    <td>19</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>20</td>
+    <td>280</td>
+  </tr>
+</table>
+	<br />
+            <table width="100%" border="1">
+          <tr>
+            <th scope="col">Step</th>
+            <th scope="col">Temperature &deg;C</th>
+            <th scope="col">Time</th>
+          </tr>
+          <tr>
+            <th scope="row">1</th>
+            <td>98</td>
+            <td>3 min</td>
+          </tr>
+          <tr>
+            <th scope="row">2</th>
+            <td>98</td>
+            <td>30 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">3</th>
+            <td>55</td>
+            <td>30 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">4</th>
+            <td>72</td>
+            <td>1 min 45 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">5</th>
+            <td>Go To 2</td>
+            <td>30x</td>
+          </tr>
+          <tr>
+            <th scope="row">6</th>
+            <td>72</td>
+            <td>4min</td>
+          </tr>
+          <tr>
+            <th scope="row">7</th>
+            <td>8</td>
+            <td>infinite</td>
+          </tr>
+        </table>
+        <p>Run overnight</p>
+</div>
+</fieldset>
+</div>
+<!-- 25.06.14 -->
+<div class="notebooky-entry">
+<h2 class="title">
+	<a name="25.06.2014">25.06.2014</a>
+</h2>
+<fieldset class="exp">
+    <legend><a name="exp_3">Sequencing  results of constructs from 23.06.2014</a></legend>
+    <div class="exp-content">
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Premix</th>
+    <th scope="col">Label-Nr.</th>
+    <th scope="col">Construct</th>
+    <th scope="col">Result</th>
+  </tr>
+  <tr>
+    <th scope="row">1</th>
+    <td>AGB0023<strong>402</strong></td>
+    <td>piGEM-018  (pMAD-DARPin)</td>
+    <td>Correct insertion of  DARPin</td>
+  </tr>
+  <tr>
+    <th scope="row">2</th>
+    <td>AGB0023<strong>403</strong></td>
+    <td>piGEM-018  (pMAD-DARPin)</td>
+    <td>Did not work</td>
+  </tr>
+  <tr>
+    <th scope="row">3</th>
+    <td>AGB0023<strong>404</strong></td>
+    <td>pMAD-Hag-Flank-cup1-1</td>
+    <td>Correct insertion,  point mutation refers to bad sequencing</td>
+  </tr>
+  <tr>
+    <th scope="row">4</th>
+    <td>AGB0023<strong>405</strong></td>
+    <td>pMAD-Hag-Flank-cup1-1</td>
+    <td>Did not work</td>
+  </tr>
+  <tr>
+    <th scope="row">5</th>
+    <td>AGB0023<strong>406</strong></td>
+    <td>piGEM-002 (Nose  plasmid)</td>
+    <td>Correct insertion of  the CM resistance</td>
+  </tr>
+</table>
+    </div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.39">18.39 Gel cPCR with picked clones from 18.38 ligation attempt transformation</a></legend>
+    <div class="aim">
+    <p>Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pet24d</p>
+    </div>
+    <div class="exp-content">
+    <p>Gel electrophoresis: no bands except for the controls were seen. The PCR has to be repeated with more colony in the PCR tubes or the prepped plasmids</p>
+    </div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.40">18.40 test digest with Nco/Bam of prepped plasmids from picked colonies</a></legend>
+    <div class="aim">
+    <p>Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pet24d</p>
+    </div>
+    <div class="exp-content">
+    <p>The picked clones from the ligation attempts 18.38 were prepped. In  order to check the insertion of the Hag/ Hag-DARPin domain the plasmids were  digested with Nco1/ BamH1 so that the gel should show the insert of 1 or 1,5 bp  length and the pet24d backbone at 5300 bp. Because of an unavailable marker as  a control the PCR amplified inserts which were used for the ligation will  run&nbsp; with the gel as well. piGEM-001 will  also be cut Nco/Bam in order to receive a marker band for the pet24d backbone.</p>
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Component</th>
+    <th scope="col">Volume (&micro;L)</th>
+    <th scope="col">Mastermix for 8 attempts</th>
+  </tr>
+  <tr>
+    <th scope="row">Plasmid (ca. 45 ng/&micro;L</th>
+    <td>5</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Cutsmart 10x</th>
+    <td>-</td>
+    <td>4</td>
+  </tr>
+  <tr>
+    <th scope="row">NcoI</th>
+    <td>-</td>
+    <td>0,5</td>
+  </tr>
+  <tr>
+    <th scope="row">BamH1</th>
+    <td>-</td>
+    <td>0,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Water</th>
+    <td>-</td>
+    <td>35</td>
+  </tr>
+  <tr>
+    <th scope="row">Mastermix</th>
+    <td>5</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>10</td>
+    <td>40</td>
+  </tr>
+</table>
+</div>
+</fieldset>
+<fieldset class="exp20">
+    <legend><a name="exp20.6">20.6 Purification of  cPCR samples with Gel extraction kit</a></legend>
+    <div class="aim">
+    <p>Aim: purification of  samples for sequencing</p>
+    </div>
+    <div class="exp-content">
+    <p>Purified samples:<br />
+    clone 3 & 5 from transformed piGEM-005<br />clone 3 & 9 from transformed piGEM-018
+    </p>
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Clone</th>
+    <th scope="col">Concentration (ng/&micro;l)</th>
+  </tr>
+  <tr>
+    <th scope="row">Hag 3</th>
+    <td>10</td>
+  </tr>
+  <tr>
+    <th scope="row">Hag 5</th>
+    <td>14</td>
+  </tr>
+  <tr>
+    <th scope="row">Hag-DARPin 3</th>
+    <td>9</td>
+  </tr>
+  <tr>
+    <th scope="row">Hag-DARPin 9</th>
+    <td>9</td>
+  </tr>
+</table>
+    </div>
+</fieldset>
+</div>
+<!-- 26.06.14 -->
+<div class="notebooky-entry">
+<h2 class="title">
+	<a name="26.06.2014">26.06.2014</a>
+</h2>
+<fieldset class="exp20">
+    <legend><a name="exp20.7">20.7 PCR with purified cPCR samples from 20.x</a></legend>
+    <div class="aim">
+    <p>Aim: PCR amplification of purified cPCR samples</p>
+    </div>
+    <div class="exp-content">
+    <p>The concentration of the cPCR samples after purification was too low for sequencing. Therefore the cPCR samples have to be amplified with PCR again.</p>
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Content</th>
+    <th scope="col">Volume (&micro;L)</th>
+    <th scope="col">MM for 6 attempts (&micro;L)</th>
+  </tr>
+  <tr>
+    <th scope="row">Purified cPCR product from 20.x<br />
+&nbsp;(3 &amp; 5 from pet-Hag, 3 &amp; 9 from  pet-Hag-DARPin)</th>
+    <td>1</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Primer Flo 54 </th>
+    <td>-</td>
+    <td>6</td>
+  </tr>
+  <tr>
+    <th scope="row">Primer Flo 56</th>
+    <td>-</td>
+    <td>6</td>
+  </tr>
+  <tr>
+    <th scope="row">Phusion</th>
+    <td>-</td>
+    <td>6</td>
+  </tr>
+  <tr>
+    <th scope="row">Phusion Buffer 5x</th>
+    <td>-</td>
+    <td>6</td>
+  </tr>
+  <tr>
+    <th scope="row">dNTP-mix</th>
+    <td>-</td>
+    <td>60</td>
+  </tr>
+  <tr>
+    <th scope="row">Water</th>
+    <td>-</td>
+    <td>216</td>
+  </tr>
+  <tr>
+    <th scope="row">Mastermix</th>
+    <td>19</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>20</td>
+    <td>300</td>
+  </tr>
+</table>
+	<br />
+            <table width="100%" border="1">
+          <tr>
+            <th scope="col">Step</th>
+            <th scope="col">Temperature &deg;C</th>
+            <th scope="col">Time</th>
+          </tr>
+          <tr>
+            <th scope="row">1</th>
+            <td>98</td>
+            <td>3 min</td>
+          </tr>
+          <tr>
+            <th scope="row">2</th>
+            <td>98</td>
+            <td>30 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">3</th>
+            <td>55</td>
+            <td>30 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">4</th>
+            <td>72</td>
+            <td>1 min 45 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">5</th>
+            <td>Go To 2</td>
+            <td>30x</td>
+          </tr>
+          <tr>
+            <th scope="row">6</th>
+            <td>72</td>
+            <td>4min</td>
+          </tr>
+          <tr>
+            <th scope="row">7</th>
+            <td>8</td>
+            <td>infinite</td>
+          </tr>
+        </table>
+    </div>
+</fieldset>
+<fieldset class="exp20">
+    <legend><a name="exp20.8">20.8 Sequencing  of purified cPCR samples from pMAD transformation </a></legend>
+    <div class="exp-content">
+        <table width="100%" border="1">
+  <tr>
+    <th scope="col">Premix</th>
+    <th scope="col">Label-Nr.</th>
+    <th scope="col">Construct</th>
+    <th scope="col">Primer</th>
+  </tr>
+  <tr>
+    <th scope="row">1</th>
+    <td>AGB0023<strong>407</strong></td>
+    <td>Hag-Spe1 in B.s.  genome clone 3</td>
+    <td>Hag-Nco-fw</td>
+  </tr>
+  <tr>
+    <th scope="row">2</th>
+    <td>AGB0023<strong>408</strong></td>
+    <td>Hag-Spe1 in B.s.  genome clone 5</td>
+    <td>Hag-Nco-fw</td>
+  </tr>
+  <tr>
+    <th scope="row">3</th>
+    <td>AGB0023<strong>409</strong></td>
+    <td>Hag-Spe1-DARPin  in B.s. genome clone 3</td>
+    <td>Hag-Nco-fw</td>
+  </tr>
+  <tr>
+    <th scope="row">4</th>
+    <td>AGB0023<strong>410</strong></td>
+    <td>Hag-Spe1-DARPin  in B.s. genome clone 9</td>
+    <td>Hag-Nco-fw</td>
+  </tr>
+</table>
+    </div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.41">18.41 new ligation of pet24d  and PCR Hag/ Hag-DARPin fragments cut Nco/Bam transformation</a></legend>
+    <div class="aim">
+    <p>Aim: ligation of construct with pet24d for overproduction of flagellin and crystallization</p>
+    </div>
+    <div class="exp-content">
+    <p>The cut  pet24d Nco/Bam which was used for the previous ligations was not purified and  contained an 1 kb insert. For a new cealn ligation the attempt was repreated  with pet24d cut by Carina Knauer .The Nco/cut Flagellin PCR products (from  clone 7 and piGEM-005) were ligated with Nco1 and BamH1 cut pet24d. </p>
+    <p>The  attempts were carried out in double. The attempts 1 &amp; 2 were incubated 1h  at room temperature and finally transformed into E. Coli XL1-Blue after  inactivation at 65 for 10 min. The attempts 1.1 and 2.1 were incubated  overnight at room temperature. 1 &micro;L of cut vector was transformed as a negative  control in order to check the amount of religants.</p>
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Component</th>
+    <th scope="col">Pet-Hag attempt (&micro;L) &ndash; 1 &amp; 1.1</th>
+    <th scope="col">Pet-Hag-DARPin attempt (&micro;L) 2&amp; 2.1</th>
+  </tr>
+  <tr>
+    <th scope="row">Insert (PCR fragments) (ca. 260 ng/&micro;L)</th>
+    <td>3</td>
+    <td>3</td>
+  </tr>
+  <tr>
+    <th scope="row">Vector (pet24d, c= 86ng/&micro;L)</th>
+    <td>5</td>
+    <td>5</td>
+  </tr>
+  <tr>
+    <th scope="row">Ligase-Buffer 10x</th>
+    <td>2</td>
+    <td>2</td>
+  </tr>
+  <tr>
+    <th scope="row">T4 Ligase</th>
+    <td>1</td>
+    <td>1</td>
+  </tr>
+  <tr>
+    <th scope="row">Millipore water</th>
+    <td>9</td>
+    <td>9</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>20</td>
+    <td>20</td>
+  </tr>
+</table>
+</div>
+</fieldset>
+</div>
+<!-- 27.06.14 -->
+<div class="notebooky-entry">
+<h2 class="title">
+	<a name="27.06.2014">27.06.2014</a>
+</h2>
+<fieldset class="exp18">
+    <legend><a name="exp18.42">18.42 Miniprep of ligation clones</a></legend>
+    <div class="exp-content">
+    <p>The  ligation between pet24d and the Hag-/Hag-DARPin fragments which were both cut  Nco/Bam was successful. The ligation plates showed over 20 clones each whereby  on the negative control&nbsp; grew a few clones  as well which were very small and sticking together. Bad plate out might be the  reason for that. In order to analyse the insert of the clones 5 clones per  ligation plate 1 and 2 were used to inoculate minipreps in 5 mL LB-Can. For the  Ligation 1 Pet-Hag clones 1-5 were picked, as well as clones 6-10 from Plate  Ligation 2 Pet-Hag-DARPin. </p>
+    <p>The  cultures were inoculated overnight at 37&deg;C.</p>
+</div>
+</fieldset>
+</div>
+<!-- 28.06.14 -->
+<div class="notebooky-entry">
+<h2 class="title">
+	<a name="28.06.2014">28.06.2014</a>
+</h2>
+<fieldset class="exp18">
+    <legend><a name="exp18.42">18.42 Miniprep of ligation clones</a></legend>
+    <div class="exp-content">
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Construct</th>
+    <th scope="col">Clone</th>
+    <th scope="col">Concentration (ng/&micro;L)</th>
+  </tr>
+  <tr>
+    <th scope="row">Pet-Hag</th>
+    <td>1</td>
+    <td>50</td>
+  </tr>
+  <tr>
+    <th scope="row">Pet-Hag</th>
+    <td>2</td>
+    <td>87</td>
+  </tr>
+  <tr>
+    <th scope="row">Pet-Hag</th>
+    <td>3</td>
+    <td>65</td>
+  </tr>
+  <tr>
+    <th scope="row">Pet-Hag-DARPin</th>
+    <td>6</td>
+    <td>83</td>
+  </tr>
+  <tr>
+    <th scope="row">Pet-Hag-DARPin</th>
+    <td>7</td>
+    <td>59</td>
+  </tr>
+</table>
+    </div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.43">18.43 cPCR of clones from 18.42</a></legend>
+    <div class="aim">
+    <p>Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pet24d</p>
+    </div>
+    <div class="exp-content">
+    <p>Plasmid  from prepped clones from each plate were analysed via cPCR with the primers flo54  and flo56 (Hag-fw and Hag-rv). The result should be a ca. 1kb fragment for  correct pet24d-Hag containing clones and a 1,5 kb fragment for  pet24d-Hag-DARPin containing clones.</p>
+        <table width="100%" border="1">
+  <tr>
+    <th scope="col">Content</th>
+    <th scope="col">Volume (&micro;L)</th>
+    <th scope="col">MM for 6 attempts (&micro;L)</th>
+  </tr>
+  <tr>
+    <th scope="row">Picked clones from 18.42<br />(1-3pet-Hag, 6-7 from pet-Hag-DARPin)</th>
+    <td>0,5</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Primer Flo 54 </th>
+    <td>-</td>
+    <td>3</td>
+  </tr>
+  <tr>
+    <th scope="row">Primer Flo 56</th>
+    <td>-</td>
+    <td>3</td>
+  </tr>
+  <tr>
+    <th scope="row">Phusion</th>
+    <td>-</td>
+    <td>3</td>
+  </tr>
+  <tr>
+    <th scope="row">Phusion Buffer 5x</th>
+    <td>-</td>
+    <td>6</td>
+  </tr>
+  <tr>
+    <th scope="row">dNTP-mix</th>
+    <td>-</td>
+    <td>24</td>
+  </tr>
+  <tr>
+    <th scope="row">Water</th>
+    <td>-</td>
+    <td>81</td>
+  </tr>
+  <tr>
+    <th scope="row">Mastermix</th>
+    <td>19,5</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>20</td>
+    <td>120</td>
+  </tr>
+</table>
+	<br />
+            <table width="100%" border="1">
+          <tr>
+            <th scope="col">Step</th>
+            <th scope="col">Temperature &deg;C</th>
+            <th scope="col">Time</th>
+          </tr>
+          <tr>
+            <th scope="row">1</th>
+            <td>98</td>
+            <td>3 min</td>
+          </tr>
+          <tr>
+            <th scope="row">2</th>
+            <td>98</td>
+            <td>30 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">3</th>
+            <td>55</td>
+            <td>30 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">4</th>
+            <td>72</td>
+            <td>1 min 45 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">5</th>
+            <td>Go To 2</td>
+            <td>30x</td>
+          </tr>
+          <tr>
+            <th scope="row">6</th>
+            <td>72</td>
+            <td>4min</td>
+          </tr>
+          <tr>
+            <th scope="row">7</th>
+            <td>8</td>
+            <td>infinite</td>
+          </tr>
+        </table>
+</div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.44">18.44 test digest with Nco/Bam – Checking insertion of Hag/-DARPin into pet24d</a></legend>
+    <div class="aim">
+    <p>Aim: proving insertion of Hag/-DARPin fragment into pet24d</p>
+    </div>
+    <div class="exp-content">
+    <p>The plasmids were digested with Nco1 and BamH1. In case of a correct insertion the pet24d backbone and the insert should be seen on the gel at 5300 bp and 1000/ 1500 bp. As control Pet24d-Hag-Flank (piGEM-001) is used to check the mastermix.</p>
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Component</th>
+    <th scope="col">Volume (&micro;L)</th>
+    <th scope="col">Mastermix(6 attempts)</th>
+  </tr>
+  <tr>
+    <th scope="row">Plasmid from clone <br />
+      ( Pet-Hag 1-3, Pet-Hag-DARPin 6 & 7)</th>
+    <td>5</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Cutsmart 10x</th>
+    <td>-</td>
+    <td>3</td>
+  </tr>
+  <tr>
+    <th scope="row">NcoI</th>
+    <td>-</td>
+    <td>0,5</td>
+  </tr>
+  <tr>
+    <th scope="row">BamHI</th>
+    <td>-</td>
+    <td>0,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Water</th>
+    <td>-</td>
+    <td>26</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>10</td>
+    <td>30</td>
+  </tr>
+</table>
+	<br />
+    <img src="https://static.igem.org/mediawiki/2014/d/dc/MR_2014-06-28_18.44.png" width="30%" />
+    </div>
+</fieldset>
+<fieldset class="exp20">
+    <legend><a name="exp20.9">20.9 Gel Purification of amplified cPCR products</a></legend>
+    <div class="aim">
+    <p>Aim: Purification for more efficient sequencing</p>
+    </div>
+    <div class="exp-content">
+    <p>The PCR product of the  amplification of cPCR products was not pure considering different bands on the  gel next to the right one. In order to exclude sequencing mistakes the PCR  attempts were purified via gel extraction of the 1,5 kb band in case of the  Hag-DARPin construct.</p>
+</div>
+</fieldset>
+<fieldset class="exp20">
+    <legend><a name="exp20.8">20.8  PCR with Gel Purified Hag-DARPin cPCR products for sequencing</a></legend>
+    <div class="aim">
+    <p>Aim: amplification of purified Hag-DARPin fragment for sequencing</p>
+    </div>
+    <div class="exp-content">
+    <p>The purified cPCR product from 20.x has to be amplified again in order to get a higher concentration for sequencing. </p>
+            <table width="100%" border="1">
+  <tr>
+    <th scope="col">Content</th>
+    <th scope="col">Volume (&micro;L)</th>
+    <th scope="col">MM for 2 attempts (&micro;L)</th>
+  </tr>
+  <tr>
+    <th scope="row">Purified PCR product from 20.x<br />(Hag-/ Hag-DARPin fragment)</th>
+    <td>1-2</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Primer Flo 54 </th>
+    <td>-</td>
+    <td>1</td>
+  </tr>
+  <tr>
+    <th scope="row">Primer Flo 56</th>
+    <td>-</td>
+    <td>1</td>
+  </tr>
+  <tr>
+    <th scope="row">Phusion</th>
+    <td>-</td>
+    <td>1</td>
+  </tr>
+  <tr>
+    <th scope="row">Phusion Buffer 5x</th>
+    <td>-</td>
+    <td>2</td>
+  </tr>
+  <tr>
+    <th scope="row">dNTP-mix</th>
+    <td>-</td>
+    <td>20</td>
+  </tr>
+  <tr>
+    <th scope="row">Water</th>
+    <td>-</td>
+    <td>75</td>
+  </tr>
+  <tr>
+    <th scope="row">Mastermix</th>
+    <td>19</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>20</td>
+    <td>100</td>
+  </tr>
+</table>
+	<br />
+            <table width="100%" border="1">
+          <tr>
+            <th scope="col">Step</th>
+            <th scope="col">Temperature &deg;C</th>
+            <th scope="col">Time</th>
+          </tr>
+          <tr>
+            <th scope="row">1</th>
+            <td>98</td>
+            <td>3 min</td>
+          </tr>
+          <tr>
+            <th scope="row">2</th>
+            <td>98</td>
+            <td>30 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">3</th>
+            <td>55</td>
+            <td>30 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">4</th>
+            <td>72</td>
+            <td>1 min 45 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">5</th>
+            <td>Go To 2</td>
+            <td>35x</td>
+          </tr>
+          <tr>
+            <th scope="row">6</th>
+            <td>72</td>
+            <td>4min</td>
+          </tr>
+          <tr>
+            <th scope="row">7</th>
+            <td>8</td>
+            <td>infinite</td>
+          </tr>
+        </table>
+    </div>
+</fieldset>
+<fieldset class="exp">
+    <legend><a name="exp_4">Transformation</a></legend>
+    <div class="exp-content">
+        <table width="100%" border="1">
+  <tr>
+    <th scope="col">Plasmid</th>
+    <th scope="col">Concentration (ng/&micro;L)</th>
+    <th scope="col">Antibiotic</th>
+    <th scope="col">Cells</th>
+    <th scope="col">Volume (&micro;L)</th>
+  </tr>
+  <tr>
+    <th scope="row">Pet-Hag clone 2</th>
+    <td>87</td>
+    <td>Can</td>
+    <td>DH5&alpha;</td>
+    <td>1</td>
+  </tr>
+  <tr>
+    <th scope="row">Pet-Hag clone 3</th>
+    <td>65</td>
+    <td>Can</td>
+    <td>DH5&alpha;</td>
+    <td>1</td>
+  </tr>
+  <tr>
+    <th scope="row">Pet-Hag-DARPin clone 7</th>
+    <td>59</td>
+    <td>Can</td>
+    <td>DH5&alpha;</td>
+    <td>1</td>
+  </tr>
+  <tr>
+    <th scope="row">Gibson Pet-Hag-Cup1-1</th>
+    <td>-</td>
+    <td>Can</td>
+    <td>DH5&alpha;</td>
+    <td>20</td>
+  </tr>
+</table>
+    </div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.45">18.45 Spe1  digest of Pet-Hag (piGEM-019)</a></legend>
+    <div class="aim">
+    <p>Aim: linearizing Pet24d-Hag with Spe1 site for a Gibson assembly with Cup1-1</p>
+    </div>
+    <div class="exp-content">
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Component</th>
+    <th scope="col">Volume (&micro;L)</th>
+  </tr>
+  <tr>
+    <th scope="row">piGEM-016 (ng/&micro;L)</th>
+    <td>17</td>
+  </tr>
+  <tr>
+    <th scope="row">Cutsmart 10x</th>
+    <td>2</td>
+  </tr>
+  <tr>
+    <th scope="row">Spe1</th>
+    <td>0,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Water</th>
+    <td>0,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>20</td>
+  </tr>
+</table>
+	<p>Incubation 1h  at 37&deg;C with following heat shock at 80&deg;C</p>
+</div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.46">18.46 Gibson assembly with linearized Pet-Hag (piGEM-019) and Cup1-1</a></legend>
+    <div class="aim">
+    <p>Aim: Insertion of Cup1-1 domain into Pet-Hag construct for crystallization</p>
+    </div>
+    <div class="exp-content">
+    <p>As insert cup1-1 PCR product from 15.55 and Spe1 cut piGEM-016 from 18.44 were used for a new Gibson assembly.<br />
+      PCR fragment cup1-1 (464 ng/&micro;L)    <br />
+      Spe1 cut pIGEM-005 ( ng/&micro;L)    </p>
+      <table width="100%" border="1">
+  <tr>
+    <th scope="col">Component</th>
+    <th scope="col">Volume (&micro;l)</th>
+  </tr>
+  <tr>
+    <th scope="row">Gibson-mix</th>
+    <td>15</td>
+  </tr>
+  <tr>
+    <th scope="row">Insert (cup1-1 464 ng/&micro;L)</th>
+    <td>2,5</td>
+  </tr>
+  <tr>
+    <th scope="row">piGEM-019</th>
+    <td>2,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>20</td>
+  </tr>
+</table>
+	<p>The mix was incubated 5 min at room temperature and then for 1h at 50&deg;C.</p>
+	<p>In the end the whole mix was transformed into E.Coli XL1-Blue and plated  out on LB-Amp. Incubation was done overnight at 37&deg;C.</p>
+</div>
+</fieldset>
+</div>
+<!-- 29.06.14 -->
+<div class="notebooky-entry">
+<h2 class="title">
+	<a name="29.06.2014">29.06.2014</a>
+</h2>
+<fieldset class="exp18">
+    <legend><a name="exp18.47">18.47 cPCR of Gibson assembly lones of Pet-Hag (piGEM-019) and Cup1-1</a></legend>
+    <div class="aim">
+    <p>Aim: screening clones for right insert</p>
+    </div>
+    <div class="exp-content">
+    <p>In order to screen the clones for  the right insertion of cup1-1 4 clones were picked from the LB-Can plate and  transferred to a LB-Can Master plate. Additionally the clones were used for  inoculation of minipreps and also cooked in 50 &micro;L dest. Water for 10 min at  95&deg;C. The lysate was used as template.</p>
+    <p>The PCR with Flo54 and iGEM-025  should generate a 785 bp fragment and the one with iGEM-024 and -025 the 164bp  domain fragment.</p>
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Content</th>
+    <th scope="col">Volume (&micro;L)</th>
+    <th scope="col">MM 1 for 5 attempts (&micro;L)</th>
+    <th scope="col">MM 2 for 5 attempts (&micro;L)</th>
+  </tr>
+  <tr>
+    <th scope="row"><p>Cooked lysate solution from clones 1-4</p></th>
+    <td>3</td>
+    <td>-</td>
+    <td>&nbsp;</td>
+  </tr>
+  <tr>
+    <th scope="row">Primer Flo 54 </th>
+    <td>-</td>
+    <td>2,5</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Primer iGEM-024</th>
+    <td>-</td>
+    <td>-</td>
+    <td>2,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Primer iGEM-025</th>
+    <td>-</td>
+    <td>-</td>
+    <td>2,5</td>
+  </tr>
+  <tr>
+    <th scope="row">dNTP-mix</th>
+    <td>-</td>
+    <td>2,5</td>
+    <td>2,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Phusion</th>
+    <td>-</td>
+    <td>5</td>
+    <td>5</td>
+  </tr>
+  <tr>
+    <th scope="row">Phusion Buffer 5x</th>
+    <td>-</td>
+    <td>20</td>
+    <td>20</td>
+  </tr>
+  <tr>
+    <th scope="row">Water</th>
+    <td>-</td>
+    <td>67,5</td>
+    <td>67,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Mastermix</th>
+    <td>17</td>
+    <td>-</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>20</td>
+    <td>100</td>
+    <td>100</td>
+  </tr>
+</table>
+	<br />
+      <table width="100%" border="1">
+          <tr>
+            <th scope="col">Step</th>
+            <th scope="col">Temperature &deg;C</th>
+            <th scope="col">Time</th>
+          </tr>
+          <tr>
+            <th scope="row">1</th>
+            <td>98</td>
+            <td>3 min</td>
+          </tr>
+          <tr>
+            <th scope="row">2</th>
+            <td>98</td>
+            <td>30 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">3</th>
+            <td>55</td>
+            <td>30 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">4</th>
+            <td>72</td>
+            <td>1 min 45 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">5</th>
+            <td>Go To 2</td>
+            <td>35x</td>
+          </tr>
+          <tr>
+            <th scope="row">6</th>
+            <td>72</td>
+            <td>4min</td>
+          </tr>
+          <tr>
+            <th scope="row">7</th>
+            <td>8</td>
+            <td>infinite</td>
+          </tr>
+        </table>
+        <p>The PCR showed no bands. The  colonies were used for minipreps so that the isolated plasmid can the used for  analysis of the insert.</p>
+</div>
+</fieldset>
+</div>
+<!-- 30.06.14 -->
+<div class="notebooky-entry">
+<h2 class="title">
+	<a name="30.06.2014">30.06.2014</a>
+</h2>
+<fieldset class="exp18">
+    <legend><a name="exp18.48">18.48 miniprep of clones from Gibson assembly with Pet-Hag (piGEM-019) and Cup1-1</a></legend>
+    <div class="aim">
+    <p>Aim: isolation of Plasmid DNA for further experiments</p>
+    </div>
+    <div class="exp-content">
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Construct</th>
+    <th scope="col">Clone</th>
+    <th scope="col">Concentration (ng/&micro;L)</th>
+  </tr>
+  <tr>
+    <th scope="row">Pet-Hag-Cup1-1</th>
+    <td>1</td>
+    <td>122</td>
+  </tr>
+  <tr>
+    <th scope="row">Pet-Hag-Cup1-1</th>
+    <td>2</td>
+    <td>85</td>
+  </tr>
+  <tr>
+    <th scope="row">Pet-Hag-Cup1-1</th>
+    <td>3</td>
+    <td>172</td>
+  </tr>
+  <tr>
+    <th scope="row">Pet-Hag-Cup1-1</th>
+    <td>4</td>
+    <td>116</td>
+  </tr>
+</table>
+    </div>
+</fieldset>
+<fieldset class="exp">
+    <legend><a name="exp_5">Sequencing</a></legend>
+    <div class="exp-content">
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Premix</th>
+    <th scope="col">Label-Nr.</th>
+    <th scope="col">Construct</th>
+    <th scope="col">Primers</th>
+  </tr>
+  <tr>
+    <th scope="row">1</th>
+    <td>AGB0023<strong>411</strong></td>
+    <td>Pet24d-Hag-Spe1  construct cl. 2</td>
+    <td>Hag-Nco-fw</td>
+  </tr>
+  <tr>
+    <th scope="row">2</th>
+    <td>AGB0023<strong>412</strong></td>
+    <td>Pet24d-Hag-DARPin  construct cl. 7</td>
+    <td>Hag-Nco-fw</td>
+  </tr>
+</table>
+    </div>
+</fieldset>
+<fieldset class="exp18">
+    <legend><a name="exp18.48">18.48 PCR of prepped Gibson assembly clones ( Pet-Hag (piGEM-019) and Cup1-1)</a></legend>
+    <div class="aim">
+    <p>Aim: screening clones for right insert</p>
+    </div>
+    <div class="exp-content">
+    <p>The isolated plasmid 1:10 diluted from the picked clones 1-4 were used as PCR template.</p>
+    <p>The PCR with Flo54 and iGEM-025  should generate a 785 bp fragment and the one with iGEM-024 and -025 the 164bp  domain fragment.</p>
+        <table width="100%" border="1">
+  <tr>
+    <th scope="col">Content</th>
+    <th scope="col">Volume (&micro;L)</th>
+    <th scope="col">MM 1 for 5 attempts (&micro;L)</th>
+    <th scope="col">MM 2 for 5 attempts (&micro;L)</th>
+  </tr>
+  <tr>
+    <th scope="row"><p>Cooked lysate solution from clones 1-4 (1:10)</p></th>
+    <td>3</td>
+    <td>-</td>
+    <td>&nbsp;</td>
+  </tr>
+  <tr>
+    <th scope="row">Primer Flo 54 </th>
+    <td>-</td>
+    <td>2,5</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Primer iGEM-024</th>
+    <td>-</td>
+    <td>-</td>
+    <td>2,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Primer iGEM-025</th>
+    <td>-</td>
+    <td>2,5</td>
+    <td>2,5</td>
+  </tr>
+  <tr>
+    <th scope="row">dNTP-mix</th>
+    <td>-</td>
+    <td>2,5</td>
+    <td>2,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Phusion</th>
+    <td>-</td>
+    <td>5</td>
+    <td>5</td>
+  </tr>
+  <tr>
+    <th scope="row">Phusion Buffer 5x</th>
+    <td>-</td>
+    <td>20</td>
+    <td>20</td>
+  </tr>
+  <tr>
+    <th scope="row">Water</th>
+    <td>-</td>
+    <td>67,5</td>
+    <td>67,5</td>
+  </tr>
+  <tr>
+    <th scope="row">Mastermix</th>
+    <td>17</td>
+    <td>-</td>
+    <td>-</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>20</td>
+    <td>100</td>
+    <td>100</td>
+  </tr>
+</table>
+	<br />
+      <table width="100%" border="1">
+          <tr>
+            <th scope="col">Step</th>
+            <th scope="col">Temperature &deg;C</th>
+            <th scope="col">Time</th>
+          </tr>
+          <tr>
+            <th scope="row">1</th>
+            <td>98</td>
+            <td>3 min</td>
+          </tr>
+          <tr>
+            <th scope="row">2</th>
+            <td>98</td>
+            <td>30 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">3</th>
+            <td>55</td>
+            <td>30 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">4</th>
+            <td>72</td>
+            <td>1 min 45 sec</td>
+          </tr>
+          <tr>
+            <th scope="row">5</th>
+            <td>Go To 2</td>
+            <td>35x</td>
+          </tr>
+          <tr>
+            <th scope="row">6</th>
+            <td>72</td>
+            <td>4min</td>
+          </tr>
+          <tr>
+            <th scope="row">7</th>
+            <td>8</td>
+            <td>infinite</td>
+          </tr>
+        </table>
+        <p>No bands were shown on the gel. The PCR was repeated with Q5 mastermix to exclude the disfunction of the polymerase.</p>
+</div>
+</fieldset>
+<fieldset class="exp20">
+    <legend><a name="exp20.9">20.9 inoculation of preculture from Bacillus WT 3610</a></legend>
+    <div class="aim">
+    <p>Aim:Preparation of for mainculture the next day</p>
+    </div>
+    <div class="exp-content">
+    <p>2x6 mL of LB were inoculated with  Bacillus WT3610 from an LB plate and incubated at 37&deg;C overnight.</p>
+</div>
+</fieldset>
+</div>
+</html>
 {{Team:Marburg/Template:End}}

Team:Marburg:Project:Notebook:June

From 2014.igem.org

Revision as of 15:59, 12 October 2014

Notebook: June