Team:TCU Taiwan/Notebook

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          <font face="Trebuchet MS" size="4" color="#333">Team uniform under design. </font>
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Revision as of 15:11, 7 October 2014

 
Notebook
 

Notebook

You should make use of the calendar feature on the wiki and start a lab notebook. This may be looked at by the judges to see how your work progressed throughout the summer. It is a very useful organizational tool as well.

   
Week 1 6/22~6/28

experimental part:

Prepare for the competent cell.

BoBo and Ted decided to multiply plasmid within bacteria but not PCR, like this:
Transformation ( Cas9 in pSB1C3 into DH5α)
Incubate DH5α with pSB1C3

Extract plasmid with pSB1C3 from DH5α.

other part:

Prepare Human practice (ppt).
Practice presentation.
Design gRNA for AmpR.
Discuss about project. Project Name is E.Maat for now (came up by Sharon).
Order restraction enzyme(PstI、EcoRI、XbaI、SpeI).

Week 2 6/29~7/5
experimental part:

Successfully transform biobrick BBa_I13521、BBa_ K914003、BBa_ K1218011 into DH5α (plasmid: pSB1C3
Extract pSB1C3 after incubation
Use Enzyme digestion(PstI and EcoRI) to confirm whether pSB1C3 is successfully extracted
Prepared Cm. plate、LB. plate
Prepared competent cell

 

other part:

Get foundation from nearby store (yeah!!!!!)
Decided to have iGEM contest in local school as human practice

Others don’t think E.Maat is a good name, under re-consideration

Week 3 7/6~7/12
experimental part:


Extract plasmid pSB1C3 with BBa_I13521、BBa_ K914003、BBa_ K1218011

Prepare Cm. plate、LB. plate

other part:


Something wrong with gRNA for AmpR, redesign

Second project theme came out by Denise and Regina: Trogene horse. Needs later discuss to decided which one as theme( E.Maat or Trogene Horse)

Try to get foundation from Biotechnology company on e-mail.

Prepare for igem conference in NCTU-Formosa (ppt)

Week 4 7/13~7/19
experimental part:


Incubate E.coli DH5α with BBa_I13521、BBa_ K914003、BBa_ K1218011(in pSB1C3 )

Extract pSB1C3 BBa_I13521、BBa_ K914003、BBa_ K1218011

other part:


Final Theme decided: Trogene Horse

Prepare for igem conference in NCTU-Formosa (ppt)

Designing team logo and project logo

House started working on wiki

Decided to have a synthetic biology contest in National Hualien Girls’ Senior High School

Week 5 7/20~7/26
experimental part:


Incubate:

1. E.coli DH5α with BBa_I13521、BBa_ K914003、BBa_ K1218011(in pSB1C3 )

2. E.coli top10 with pBluescript II SK (-)

 

Extract :

1. pSB1C3: BBa_I13521、BBa_ K914003、BBa_ K1218011

2. pBluescript

Use Enzyme digestion(PstI and EcoRI) to confirm whether pSB1C3 and pBluescript is successfully extracted.

other part:


Prepare for igem conference in NCTU-Formosa (ppt)

Designing team logo and project logo

House working on wiki construction

Prepare for the contest in National Hualien Girls’ Senior High School (ppt)

Week 6 7/27~8/2
experimental part:


Incubate:

1. E.coli DH5α with BBa_I13521、BBa_ K914003、BBa_ K1218011(in pSB1C3 )

2. E.coli top10 with pBluescript II SK (-)

 

Extract :

1. pSB1C3: BBa_I13521、BBa_ K914003、BBa_ K1218011

2. pBluescript

Use Enzyme digestion(PstI and EcoRI) to confirm whether pSB1C3 and pBluescript is successfully extracted.

other part:


Prepare for igem conference in NCTU-Formosa (ppt).

Have a synthetic biology contest in National Hualien Girls’ Senior High School.

Order primer for gRNA team logo and project logo confirmed.

Week 7 8/3~8/7

Attending iGEM conference in NCTU-Formosa

Week 8 8/10~16
experimental part:


Incubate:

1. E.coli DH5α with BBa_I13521、BBa_ K914003、BBa_ K1218011(in pSB1C3 )

2. E.coli top10 with pBluescript II SK (-)

 

Extract :

1. pSB1C3: BBa_I13521、BBa_ K914003、BBa_ K1218011

2. pBluescript

Use Enzyme digestion(PstI and EcoRI) to confirm whether pSB1C3 and pBluescript is successfully extracted.

Purification of RFP sequence from pSB1C3 Prepare Cm. plate、LB. plate

other part:


Team uniform under design.

Week 9 8/17~8/23
experimental part:


Incubate:

1. E.coli DH5α with BBa_I13521、BBa_ K914003、BBa_ K1218011(in pSB1C3 )

2. E.coli top10 with pBluescript II SK (-)

Extract :

1. pSB1C3: BBa_I13521、BBa_ K914003、BBa_ K1218011

2. pBluescript

Use Enzyme digestion(PstI and EcoRI) to confirm whether pSB1C3 and pBluescript is successfully extracted.

Purification of RFP sequence from pSB1C3.

Week 10 8/24~8/30
experimental part:


Ligation of RFP and pBluescript SK(-)

Transformation clone RFP/pBluescript SK(-) to DH5α

Extract plasmid clone RFP/pBluescript SK(-)

Use Enzyme digestion(PstI and EcoRI) to confirm whether pSB1C3 and pBluescript is successfully extracted.

other part:


Design badge as small gift

Order Helper phage for pBluescript SK(-)

Make movie for project introduction of Trogene horse.

Prepare iGEM presentation ppt、poster.

Week 11 8/31~9/6
experimental part:


Incubate:

1. E.coli DH5α with BBa_I13521、(in pSB1C3 )

2. E.coli top10 with pBluescript II SK (-)

Extract :

1. pSB1C3: BBa_I13521

2. pBluescript

Use Enzyme digestion(PstI and EcoRI) to confirm whether pSB1C3 and pBluescript is successfully extracted

Purification of RFP sequence from pSB1C3

Ligation Clone RFP/pBluescript SK(-)to DH5α Store BBa_I13521、BBa_ K914003、BBa_ K1218011、clone RFP/pBluescript SK(-)

other part:


Make movie for project introduction of Trogene.

horse Prepare iGEM presentation ppt、poster.

Week 12 9/7~9/13
experimental part:


Ligation Clone RFP/pBluescript SK(-)

Extract plasmid clone RFP/pBluescript SK(-)

Use Enzyme digestion(PstI and EcoRI) to confirm whether pSB1C3 and pBluescript is successfully extracted

Modeling for phage injection (Thanks for NCTU-Formosa’s help)

other part:

Prepare iGEM presentation ppt、poster.

Week 13 9/14~9/20
experimental part:


Ligation Clone RFP/pBluescript SK(-)

Extractplasmid clone RFP/pBluescript SK(-)

Use Enzyme digestion(PstI and EcoRI) to confirm whether pSB1C3 and pBluescript is successfully extracted

Prepare competent cell(JM101)

incubate:

1. E.coli DH5α with BBa_I13521(pBluescript)、BBa_K1473001~3003(in pSB1C3 )

 

Extract :

1. pSB1C3: BBa_I13521、BBa_K1473001~3003

Use Enzyme digestion(PstI and EcoRI) to confirm whether pSB1C3 and pBluescript is successfully extracted

PCR: tracrRNA、Cas 9+crRNA

Modeling for phage injection

other part:


Prepare iGEM presentation ppt、poster

Wiki construction

Week 14 9/21~9/27
experimental part:


Ligation gRNA/ pSB1C3

Transformation gRNA/ pSB1C3 to DH5α

Incubate gRNA/ pSB1C3 in E.coli JM101

Extract plasmid gRNA/ pSB1C3 in E.coli JM101

Use Enzyme digestion(PstI and EcoRI) to confirm whether pSB1C3 and pBluescript is successfully extracted

PCR trRNA、Cas 9+crRNA

Prepare modeling

3 new biobrick finished

other part:


Have a iGEM contest(HP) in Tzu chi university

Prepare presentation ppt、poster

Wiki construction

Week 15 9/28~10/4
other part:


Prepare iGEM presentation ppt、poster

Wiki construction

^
   

^