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Revision as of 02:42, 3 September 2014

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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 ustoeful organizational tool as well.

7/15

transformation

Tatsui, Matsumoto and Sukegawa

Name	Sample/(µl)	Competent Cells/(µl)	Total/(µl)	Medium
BBa_J23101(Pcon)	2	20(2/23)	22	LB(CP)
BBa_B0032(RBS)	2	20(2/23)	22	LB(CP)

7/16

transformation

Tatsui )

Name	Sample/(µl)	Competent Cells/(µl)	Total/(µl)	Medium
BBa_B0030(1)	2	20(2/23)	22	LB(CP)
BBa_B0030(2)	2	20(bought)	22	LB(CP)
BBa_B0032(	2	20(2/23)	22	LB(CP)
BBa_B0032	2	20(bought)	22	LB(CP)

7/17

Colony PCR

Tatsui, Matsumoto, Li, and Yamauchi

Sample
7/16 BBa_B0030-(1)
7/16 BBa_B0030-(1)
7/16 BBa_B0030-(1)
7/16 BBa_B0030-(2)
7/16 BBa_B0030-(2)
7/16 BBa_B0030-(2)
7/16 BBa_B0032-(1)
7/16 BBa_B0032-(1)
7/16 BBa_B0032-(1)
7/16 BBa_B0032-(2)
7/16 BBa_B0032-(2)
7/16 BBa_B0032-(2)
Negative control

Liquid Culture

Tatsui, Matsumoto, Li, and Yamauchi

Sample	medium
7/16 BBa_B0030-(1)	Plusgrow medium(+CP)
7/16 BBa_B0030-(2)	Plusgrow medium(+CP)
7/16 BBa_B0030-(3)	Plusgrow medium(+CP)
7/16 BBa_B0030-(4)	Plusgrow medium(+CP)
7/16 BBa_B0030-(5)	Plusgrow medium(+CP)
7/16 BBa_B0030-(6)	Plusgrow medium(+CP)
7/16 BBa_B0032-(1)	Plusgrow medium(+CP)
7/16 BBa_B0032-(2)	Plusgrow medium(+CP)
7/16 BBa_B0032-(3)	Plusgrow medium(+CP)
7/16 BBa_B0032-(4)	Plusgrow medium(+CP)
7/16 BBa_B0032-(5)	Plusgrow medium(+CP)
7/16 BBa_B0032-(6)	Plusgrow medium(+CP)

7/18

Miniprep

Tatsui, Matsumoto, Tsujii, Stephane, and Yamauchi

DNA	Concentration(µg/ml)	260/280	260/230
7/16 BBa_B0030-(1)	229	1.96	1.40
7/16 BBa_B0030-(2)	209	1.95	1.50
7/16 BBa_B0030-(3)	108	2.12	2.12
7/16 BBa_B0030-(4)	186	-	-
7/16 BBa_B0030-(5)	174	2.02	1.56
7/16 BBa_B0030-(6)	158	2.01	1.68
7/16 BBa_B0032-(1)	179	2.00	2.06
7/16 BBa_B0032-(3)	221	1.90	1.37
7/16 BBa_B0032-(4)	225	1.89	1.37
7/16 BBa_B0032-(5)	270	1.98	1.63
7/16 BBa_B0032-(6)	194	1.89	1.33

7/28

Restriction Enzyme Digestion

No name

7/18 RBS Sample	EcoR1	Xba1	Spe1	Pst1	Buffur	BSA	MilliQ	TOTAL
Sample1	0.3	0	0	0	1(H)	0	7.7	10
Sample2	0	0.3	0	0	1(M)	1	6.7	10
Sample3	0	0	0.3	0	1(M)	0	7.7	10
Sample4	0	0	0	0.3	1(H)	0	7.7	10
Control	0	0	0	0	1	0	8	10

7/30

Restriction Enzyme Digestion

No name

7/18 RBS Sample	EcoR1	Xba1	Spe1	Pst1	Buffur	BSA	MilliQ	TOTAL
Sample1	0.3	0	0	0	1(H)	0	7.7	10
Sample2	0	0.3	0	0	1(M)	1	6.7	10
Sample3	0	0	0.3	0	1(M)	0	7.7	10
Sample4	0	0	0	0.3	1(H)	0	7.7	10
Control	0	0	0	0	1	0	8	10

7/30

Electrophoresis for confirmation

No name

Lane	Restriction Enzyme Digestion Products
1	Sample1
2	Sample2
3	Sample3
4	Sample4
5	Sample5
6	1kbp ladder

7/31

Transformation

Hashitani, Tatsui, Li and Yamauchi

	2-24B BBa_E0240(RBS-GFP-DT)+CP	4-17D J23100(Pcon) +Amp
plasmid	2μL	2μL
DH5α	20μL	2μL
TOTAL	22μL	22μL

7/31

Restriction Enzyme Digestion

Hashitani, Tatsui, Li and Yamauchi

Sample	Plasmid	EcoR1	Xba1	Spe1	Pst1	Buffur	BSA	MilliQ	TOTAL
Sample1	5	0.3	0	0	0	1(H)	0	3.7	10
Sample2	5	0	0.3	0	0	1(M)	0	3.7	10
Sample3	5	0	0	0.3	0	1(H)	0	3.7	10
Sample4	5	0	0	0	0.3	1(M)	1	2.7	10
Control	5	0	0	0	0	1(M)	0	4	10

8/1

Electrophoresis for confirmation

Honda, Li and Yamauchi

Lane	Sample
1	1kb ladder
2	7/31 Restruction Enzyme Digestion Products Sample1
3	7/31 Restruction Enzyme Digestion Products Sample2 Error
4	NC
5	NC
6	7/31 Restruction Enzyme Digestion Products Sample3
7	7/31 Restruction Enzyme Digestion Products Sample4
8	7/31 Restruction Enzyme Digestion Products Sample5

8/1

PCR

Tatsui

BBa_E0240(RBS-GFP-DT)
	Volume
10×buffur	5μL
2mMdNTPs	5μL
25mM MgSO4	2μL
VF Primer	1.5μL
VR Primer	1.5μL
template	0.5μL
KOD-plus	1μL
MilliQ	33.5μL
TOTAL	50μL

8/1

PCR

No name

BBa_E0240(RBS-GFP-DT)
	Temparature	Time
Pre Denature	94℃	2min
Denature	94℃	15sec	30cycle
Anniling	55℃	30sec	30cycle
Exensim	68℃	1min	30cycle

8/1

densitomitory after column prification

No name

BBa_E0240(RBS-GFP-DT)
Density	260/230	260/280
80μg/mL	1.78	1.91

8/2

Miniprep

Tatsui, Honda, Matsumoto, Yamauchi, Li, Tsujii, and Nakamura

7/31 Pcon
Sample	Density(μg/mL)	260/280	260/230
1	2.9	2.11	3.09
2	1.3	2.59	-
3	3.2	2.01	3.13
4	2.8	1.87	2.70
5	2.1	2.39	5.90
6	3.6	1.90	1.37

8/20

Transformation

Honda

	BBa_I732095	7/31 Transformation BBa_E0240(RBS-aFD-DT)(+CP)
plasmid	2μL	2μL
DH5α	20μL	20μL
TOTAL	22μL	22μL
	×2	×2

8/21

Colony PCR

Shimazaki

	Master Mix
Quick Taq	20μL
VF	0.8μL
VR	0.8μL
MilliQ	18.4μL
TOTAL	40μL

8/21

Colony PCR

Shimazaki

	Temparature	Time
Pre Denature	94.0℃	2min
Denature	94.0℃	30sec
Anniling	55.0℃	0.8μL
Extention	68.0℃	18.4μL
Denature - Extention 30 cycle

8/21

Electrophoresis for confirmation

Honda

Lane	Sample
1	1kb ladder
2	BBa_E0430-Sample1
3	BBa_E0430-Sample2
4	BBa_E0430-Sample3
5	Negative Control

8/21

Electrophoresis for confirmation

Honda and Tatsui

1	BBa_E0430-Sample1
2	BBa_E0430-Sample2
3	BBa_E0430-Sample3

8/22

Miniprep

Honda

Sample	density	260/280	260/230
BBa_I732095-Sample1	430µg/mL	1.68	2.13
BBa_I732095-Sample2	255µg/mL	1.87	1.81
BBa_I732095-Sample3	215µg/mL	1.78	1.35

8/22

Restriction Enzyme Digestion

Nakamura

BBa_I732095-Sample1	4.7µL
EcoRI	1µL
SpeRI	1µL
Buffur(H)	3µL
MilliQ	20.3µL
TOTAL	30µL
BBa_I732095-Sample2	7.8µL
EcoRI	1µL
SpeRI	1µL
Buffur(H)	3µL
MilliQ	20.3µL
TOTAL	30µL
BBa_I732095-Sample3	9.3µL
EcoRI	1µL
SpeRI	1µL
Buffur(H)	3µL
MilliQ	15.7µL
TOTAL	30µL

8/22

Transformation

Tatsui and Yamauchi

BBa_J04450(pSB3C5)
DNA	2µL
Conpitent cell	20µL

8/22

Transformation

Tatsui and Yamauchi

BBa_J04450(pSB3C5)	Time
on ice	30min
heat shock	45sec
on ice	2min
Preculture	1hour

8/25

Transformation

Tatsui, Kita and Li

BBa_J04450(2014)
DNA	20µL
Conpitent cell	40µL
BBa_J04450(2013)
DNA	20µL
Conpitent cell	40µL
BBa_C0051
DNA	20µL
Conpitent cell	40µL

8/25

liquid culture

Tatsui

8/22 J04450(psB3C5) 30mL

8/26

Miniprep

Tsujii, Honda and Matsumoto

Sample	density(µg/mL)	260/280	260/230
J04450(psB3C5)	575	1.37	1.34

8/26

liquid culture

Tatsui, Matsumoto and Nakamura

8/25 psB2K3×5(30mL)
8/25 psB1A2×2(12mL)

8/27

Miniprep

No name

Sample	density	260/280	260/230
8/26 licuid culture psB2K3	1045(µg/mL)	1.43	1.11
8/26 licuid culture psB1A2	790(µg/mL)	1.39	0.90

8/27

BBa_J04450(psB3T5)

No name

DNA	6mL
Tet	60µg(10µg/mL)

8/29

Miniprep

Tatsui

DNA	Concentration(µg/ml)	260/280	260/230
7/16 BBa_B0030-(1)	229	1.96	1.40

transformation

Tatsui

Name	Sample(µl)	Competent Cells(µl)	Total(µl)	Plate
BBa_J04450	2	20(2/23)	22	LB（CP）

9/1

Colony PCR

No name

Restriction Enzyme Digestion

No name

Sample	Volume	EcoR1	Pst1	Buffur(H)	MilliQ	TOTAL
8/28 pSB3T5	25	2	2	6	25	60
Control 1	3.7	0	0	1	5.3	10
8/22 I732095	14	3	3	9	61	90
Control 2	1.5	0	0	1	7.5	10
8/27 pSB2K3	6	3	3	9	69	90
Control 3	1	0	0	1	8	10
Pcon 3	20	1.5	1.5	5	17	45
Control 4	4	0	0	1	5	10
Pcon 1	20	1.5	1.5	5	17	45
Control 5	4	0	0	1	5	10

Liquid Culture

No name

Sample	Medium	Volume
8/29 BBa_J04450(pSB4A5)	Plusgrow medium(+Amp)	12ml
8/1 Pcon 1	Plusgrow medium(+Amp)	12ml
8/27 pSB3T5 1	Plusgrow medium(+Tet)	12ml
8/29 dddD+pSB1C3 1	Plusgrow medium(+CP)	3ml
8/29 dddD+pSB1C3 2	Plusgrow medium(+CP)	3ml
8/29 dddD+pSB1C3 3	Plusgrow medium(+CP)	3ml

@@ Line 139: / Line 139: @@
 <table class="note">
 <tr><th>Name</th><th>Sample/(&micro;l)</th><th>Competent Cells/(&micro;l)</th><th>Total/(&micro;l)</th><th>Medium</th></tr>
-<tr><td>BBa_B0030</td><td>2</td><td>20(2/23)</td><td>22</td><td>LB(CP)</td></tr>
+<tr><td>BBa_B0030(1)</td><td>2</td><td>20(2/23)</td><td>22</td><td>LB(CP)</td></tr>
-<tr><td>BBa_B0030</td><td>2</td><td>20(bought)</td><td>22</td><td>LB(CP)</td></tr>
+<tr><td>BBa_B0030(2)</td><td>2</td><td>20(bought)</td><td>22</td><td>LB(CP)</td></tr>
-<tr><td>BBa_B0032</td><td>2</td><td>20(2/23)</td><td>22</td><td>LB(CP)</td></tr>
+<tr><td>BBa_B0032(</td><td>2</td><td>20(2/23)</td><td>22</td><td>LB(CP)</td></tr>)
 <tr><td>BBa_B0032</td><td>2</td><td>20(bought)</td><td>22</td><td>LB(CP)</td></tr>
 </table>
@@ Line 150: / Line 150: @@
 <table class="note">
 <tr><th>Sample</th></tr>
+<tr><td>7/16 BBa_B0030-(1)</td></tr>
+<tr><td>7/16 BBa_B0030-(1)</td></tr>
 <tr><td>7/16 BBa_B0030-(1)</td></tr>
 <tr><td>7/16 BBa_B0030-(2)</td></tr>
-<tr><td>7/16 BBa_B0030-(3)</td></tr>
+<tr><td>7/16 BBa_B0030-(2)</td></tr>
-<tr><td>7/16 BBa_B0030-(4)</td></tr>
+<tr><td>7/16 BBa_B0030-(2)</td></tr>
-<tr><td>7/16 BBa_B0030-(5)</td></tr>
-<tr><td>7/16 BBa_B0030-(6)</td></tr>
 <tr><td>7/16 BBa_B0032-(1)</td></tr>
+<tr><td>7/16 BBa_B0032-(1)</td></tr>
+<tr><td>7/16 BBa_B0032-(1)</td></tr>
+<tr><td>7/16 BBa_B0032-(2)</td></tr>
+<tr><td>7/16 BBa_B0032-(2)</td></tr>
 <tr><td>7/16 BBa_B0032-(2)</td></tr>
-<tr><td>7/16 BBa_B0032-(3)</td></tr>
+<tr><td>Negative control</td></tr>
-<tr><td>7/16 BBa_B0032-(4)</td></tr>
-<tr><td>7/16 BBa_B0032-(5)</td></tr>
-<tr><td>7/16 BBa_B0032-(6)</td></tr>
-<tr><td>NC</td></tr>
 </table>

Team:Kyoto/Notebook

From 2014.igem.org

Revision as of 02:42, 3 September 2014

Notebook

7/15

transformation

7/16

transformation

7/17

Colony PCR

Liquid Culture

7/18

Miniprep

7/28

Restriction Enzyme Digestion

7/30

Restriction Enzyme Digestion

7/30

Electrophoresis for confirmation

7/31

Transformation

7/31

Restriction Enzyme Digestion

8/1

Electrophoresis for confirmation

8/1

PCR

8/1

PCR

8/1

densitomitory after column prification

8/2

Miniprep

8/20

Transformation

8/21

Colony PCR

8/21

Colony PCR

8/21

Electrophoresis for confirmation

8/21

Electrophoresis for confirmation

8/22

Miniprep

8/22

Restriction Enzyme Digestion

8/22

Transformation

8/22

Transformation

8/25

Transformation

8/25

liquid culture

8/26

Miniprep

8/26

liquid culture

8/27

Miniprep

8/27

BBa_J04450(psB3T5)

8/29

Miniprep

transformation

9/1

Colony PCR

Restriction Enzyme Digestion

Liquid Culture