Template:Kyoto/Notebook/Sep 5

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Latest revision as of 14:20, 27 September 2013

Sep 5

Electrophoresis

No name

Lane	Sample	Enzyme1	Enzyme2
1	100bp ladder	--	--
2	J23100-3	--	--
3	J23100-4	--	--
4	J23100-5	--	--
5	100bp ladder	--	--

Miniprep

Nakamoto

DNA	concentration[µg/mL]	260/280	260/230
8/3 J23100-3	349.1	1.69	1.851
8/10 Plac-2	331.3	1.84	1.42

Ligation

Kojima

state	Vector		Inserter		Ligation High ver.2
experiment	Pconst	13.2	spinach-DT	2.1	3.5
experiment	Plac	15.3	spinach-DT	2.1	3.5
experiment	Pconst	13.2	pT181 antisense (XbaI & PstI)	6.6	3.5
experiment	Plac	15.3	pT181 antisense (XbaI & PstI)	6.6	3.5
experiment	Ptet	30.1	pT181 antisense (XbaI & PstI)	6.6	3.5
experiment	Pconst	13.2	pT181 attenuator	11.7	3.5
experiment	Plac	15.3	pT181 attenuator	11.7	3.5
experiment	Ptet	30.1	RBS-lacZα-DT	3.0	3.5

incubate 16 °C 1 hour

Electrophoresis

Tatsui

Lane	Sample
1	100bp ladder
2	RBS-luxI-DT
3	Pbad/araC
4	NC
5	100bp ladder

Gel Extraction

No name

Lane	DNA	Enzyme
1	1kbp ladder
2	RBS-luxI-DT
3	RBS-luxI-DT
4
5	Pbad/araC
6	Pbad/araC

Name	concentration[µg/mL]	260/280	260/230
RBS-luxI-DT	23.2	0.83	7.89
Pbad/araC	51.8	1.20	0.11

Colony PCR

No name

Sample	base pair
9/4 aptamer 12_1R(pSB1C3)-1	384
9/4 aptamer 12_1R(pSB1C3)-2	384
9/4 pT181 antisense(pSB1C3)-1	415
9/4 pT181 antisense(pSB1C3)-2	415
9/4 pT181 antisense(pSB1C3)-3	415
9/4 pT181 antisense(pSB1C3)-4	415

PreDenature	Denature	Annealing	Extension	cycle
94°C	94°C	55°C	68°C	--
5min	30s	30s	30s	30cycles

Sample	base pair
9/4 aptamer 12_1R-DT-1	521
9/4 aptamer 12_1R-DT-2	521
9/4 aptamer 12_1R-DT-3	521
9/4 aptamer 12_1R-DT-4	521
9/4 pT181 attenuator(pSB1C3)	601
9/4 pT181 attenuator(pSB1C3)	601
9/4 RBS-lysis1-DT	613
9/4 RBS-lysis1-DT	613

PreDenature	Denature	Annealing	Extension	cycle
94°C	94°C	55°C	68°C	--
5min	30s	30s	36s	30cycles

Sample	base pair
9/4 RBS-lysis2-DT-1	985
9/4 RBS-lysis2-DT-2	985
9/4 RBS-lysis2-DT-3	985
9/4 RBS-lysis2-DT-4	985
9/4 RBS-lysis3-DT-1	1210
9/4 RBS-lysis3-DT-2	1210

PreDenature	Denature	Annealing	Extension	cycle
94°C	94°C	55°C	68°C	--
5min	30s	30s	72s	30cycles

Liquid Culture

Nakamoto

Sample	medium
8/9 J23100-5	Plusgrow medium(+Amp)

37°C

Transformation

No name

Name	Sample(µL)	Competent Cells(µL)	Total(µL)	Plate
9/5 Pconst+spinach-DT	2	20	22	--
9/5 Plac+spinach-DT	2	20	22	--
9/5 Pconst+pT181 antisense	2	20	22	--
9/5 Plac+pT181 antisense	2	20	22	--
9/5 Ptet+pT181 antisense	2	20	22	--
9/5 Plux+pT181 attenuator	2	20	22	--
9/5 Ptet+pT181 attenuator	2	20	22	--
9/5 Ptet+pT181 attenuator	2	20	22	--
9/5 Pconst+RBS-tetR+DT	2	20	22	--
9/16(2012) T7-His-FT	2	20	22	--
9/16(2012) pBr322	2	20	22	--

Restriction Enzyme Digestion

No name

	9/5 Pbad/araC	EcoRI	SpeI	XbaI	PstI	BSA	Buffer	MilliQ	total
2 cuts	4µL	0µL	1µL	0µL	1µL	3µL	3µL	18µL	30µL

	9/5 RBS-luxI-DT	EcoRI	SpeI	XbaI	PstI	BSA	Buffer	MilliQ	total
2 cuts	4µL	0µL	0µL	1µL	1µL	3µL	3µL	18µL	30µL

	8/28 Plux	EcoRI	SpeI	XbaI	PstI	BSA	Buffer	MilliQ	total
2 cuts	12µL	0µL	1µL	0µL	1µL	3µL	3µL	10µL	30µL
NC	0.6µL	0µL	0µL	0µL	0µL	1µL	1µL	7.4µL	10µL

	9/5 Pconst(J23100)	EcoRI	SpeI	XbaI	PstI	BSA	Buffer	MilliQ	total
2 cuts	5.7µL	0µL	1µL	0µL	1µL	3µL	3µL	16.3µL	30µL
NC	0.3µL	0µL	0µL	0µL	0µL	1µL	1µL	7.7µL	10µL

	9/5 Plac	EcoRI	SpeI	XbaI	PstI	BSA	Buffer	MilliQ	total
2 cuts	6.0µL	0µL	1µL	0µL	1µL	3µL	3µL	16µL	30µL
NC	0.3µL	0µL	0µL	0µL	0µL	1µL	1µL	7.7µL	10µL

	8/31 Plux-RBS-GFP-DT-1	EcoRI	SpeI	XbaI	PstI	BSA	Buffer	MilliQ	total
2 cuts	9.4µL	1µL	1µL	0µL	0µL	3µL	3µL	12.6µL	30µL
NC	0.5µL	0µL	0µL	0µL	0µL	1µL	1µL	7.5µL	10µL

	8/20 Pconst-RBS-luxR-DT	EcoRI	SpeI	XbaI	PstI	BSA	Buffer	MilliQ	total
2 cuts	4.5µL	1µL	0µL	1µL	0µL	3µL	3µL	13.5µL	30µL
NC	0.2µL	0µL	0µL	0µL	0µL	1µL	1µL	7.8µL	10µL

DNA	concentration[µg/mL]	260/280	260/230
9/5 RBS-luxI-DT	7.6	1.56	-1.42
9/5 Pbad/araC	7.5	1.54	3.84

Electrophoresis

No name

Lane	Sample	Enzyme1	Enzyme2
1	100bp ladder	--	--
2	aptamer 12_1R (pSB1C3)-1	--	--
3	aptamer 12_1R (pSB1C3)-2	--	--
4	pT181 antisense(pSB1C3)-1	--	--
5	pT181 antisense(pSB1C3)-2	--	--
6	pT181 antisense(pSB1C3)-3	--	--
7	pT181 antisense(pSB1C3)-4	--	--
8	100bp ladder	--	--

Lane	Sample	Enzyme1	Enzyme2
1	100bp ladder	--	--
2	aptamer 12_1R-DT-1	--	--
3	aptamer 12_1R-DT-2	--	--
4	aptamer 12_1R-DT-3	--	--
5	aptamer 12_1R-DT-4	--	--
6	pT181 attenuator(pSB1C3)-1	--	--
7	pT181 attenuator(pSB1C3)-2	--	--
8	RBS-lysis1-DT-1	--	--
9	RBS-lysis1-DT-2	--	--
10	100bp ladder	--	--

Lane	Sample	Enzyme1	Enzyme2
1	100bp ladder	--	--
2	RBS-lysis2-DT-1	--	--
3	RBS-lysis2-DT-2	--	--
4	RBS-lysis2-DT-3	--	--
5	RBS-lysis2-DT-4	--	--
6	RBS-lysis3-DT-1	--	--
7	RBS-lysis3-DT-2	--	--
8	100bp ladder	--	--

Lane	Sample	Enzyme1	Enzyme2
1	1kbp ladder	--	--
2	Pconst	SpeI	PstI
3	Pconst NC	--	--
4	Plac	SpeI	PstI
5	Plac NC	--	--
6	Plux	SpeI	PstI
7	Plux NC	--	--
8	Pconst-RBS-luxR-DT	EcoRI	XbaI
9	Pconst-RBS-luxR-DT NC	--	--
10	Plux-RBS-GFP-DT	EcoRI	SpeI
11	Plux-RBS-GFP-DT NC	--	--
12	1kbp ladder	--	--

5x M9 Medium (+EDTA)

Hirano

volume	10ml
Na2HPO4	60mg
KH2PO4	30mg
NaCl	5mg
NH4Cl	10mg
Fe(III)-EDTA	1263.27mg
MilliQ	up to 10 mL

autoclave at 121 °C for 20 min

Gel Extraction

No name

Lane	DNA	Enzyme
1	1kbp ladder
2	Pconst	SpeI & PstI
3	Pconst	SpeI & PstI

Name	concentration[µg/mL]	260/280	260/230
Pconst	5.3	1.98	0.06

Lane	DNA	Enzyme
1	100bp ladder
2	Plac	SpeI & PstI
3	Plac	SpeI & PstI
5	Plux	SpeI & PstI
6	Plux	SpeI & PstI

Name	concentration[µg/mL]	260/280	260/230
Plac (SpeI & PstI)	5.2	1.82	0.36
Plux(SpeI & PstI)	8.0	1.87	0.25

Lane	DNA	Enzyme
1	1kbp ladder
2	Pconst-RBS-luxR-DT	EcoRI & XbaI
3	Pconst-RBS-luxR-DT	EcoRI & XbaI
5	Plux-RBS-GFP-DT	EcoRI & SpeI
6	Plux-RBS-GFP-DT	EcoRI & SpeI

Name	concentration[µg/mL]	260/280	260/230
Pconst-RBS-luxR-DT(EcoRI & XbaI)	30.6	1.84	1.16
Plux-RBS-GFP-DT (EcoRI & SpeI)	21.8	1.87	0.98

DNA Purification

No name

DNA	concentration[µg/mL]	260/280	260/230
9/5 RBS-luxI-DT	7.6	1.56	-1.42
9/5 Pbad/araC	7.5	1.54	3.84

Miniprep

No name

DNA	concentration[µg/mL]	260/280	260/230
8/9 J23100-5	243.0	1.90	1.81

Colony PCR

No name

Sample	base pair
9/4 RBS-lysis3-DT-3	1210
9/4 RBS-lysis3-DT-4	1210
9/4 RBS-lysis3-DT-5	1210
9/4 RBS-lysis1-DT-3	613
9/4 Ptrc KaiC-1	--
9/4 pSB4K5	1370

PreDenature	Denature	Annealing	Extension	cycle
94°C	94°C	55°C	68°C	--
5min	30s	30s	1min 25s	30cycles

Liquid Culture

Hirano

Sample	medium
9/4 aptamer 12_1R-DT-1	Plusgrow medium (+CP)
9/4 pT181 attenuator(pSB1C3)-1	Plusgrow medium (+CP)
9/4 RBS-lysis2-DT-1	Plusgrow medium (+CP)
9/4 Ptrc-KaiC -1	Plusgrow medium (+Amp)
9/4 pSB4K5 -1	Plusgrow medium (+Kan)

@@ Line 16: / Line 16: @@
 |5||100bp ladder||--||--
 |}
-[[File:igku_xx.xxx]]<br>
+[[File:igku_Sep5_electrophoresis_N1.jpg]]<br>
 </div>
@@ Line 54: / Line 54: @@
 |}
 incubate 16 &deg;C 1 hour
+</div>
+===Electrophoresis===
+<div class="experiment">
+<span class="author">Tatsui</span>
+{| class="wikitable"
+!Lane||Sample
+|-
+|1||100bp ladder
+|-
+|2||RBS-luxI-DT
+|-
+|3||Pbad/araC
+|-
+|4||NC
+|-
+|5||100bp ladder
+|}
+[[File:igku_Sep5_electrophorsis_N2_1.jpg]]<br>
+[[File:igku_Sep5_electrophorsis_N2_2.jpg]]<br>
 </div>
@@ Line 68: / Line 88: @@
 |3||RBS-luxI-DT||
 |-
-|4||1kbp ladder||
+|4||||
 |-
 |5||Pbad/araC||
@@ Line 74: / Line 94: @@
 |6||Pbad/araC||
 |}
-[[File:igku_xxbeforexx.xxx]]<br>
+[[File:Igku Sep5 Gel Extraction(N3) 1.jpg]]<br>
-[[File:igku_xxafterxx.xxx]]<br>
+[[File:Igku Sep5 Gel Extraction(N3) 2.jpg]]<br>
-NOT YET</div>
 {| class="wikitable"
 !Name||concentration[&micro;g/mL]||260/280||260/230
@@ Line 93: / Line 110: @@
 !Sample||base pair
 |-
-|9/4 apt12_1R(pSB1C3)-1||384
+|9/4 aptamer 12_1R(pSB1C3)-1||384
 |-
-|9/4 apt12_1R(pSB1C3)-2||384
+|9/4 aptamer 12_1R(pSB1C3)-2||384
 |-
 |9/4 pT181 antisense(pSB1C3)-1||415
@@ Line 116: / Line 133: @@
 !Sample||base pair
 |-
-|9/4 apt12_1R-DT-1||521
+|9/4 aptamer 12_1R-DT-1||521
 |-
-|9/4 apt12_1R-DT-2||521
+|9/4 aptamer 12_1R-DT-2||521
 |-
-|9/4 apt12_1R-DT-3||521
+|9/4 aptamer 12_1R-DT-3||521
 |-
-|9/4 apt12_1R-DT-4||521
+|9/4 aptamer 12_1R-DT-4||521
 |-
 |9/4 pT181 attenuator(pSB1C3)||601
@@ Line 163: / Line 180: @@
 |5min||30s||30s||72s||30cycles
 |}
-</div>
-===Electrophoresis===
-<div class="experiment">
-<span class="author">No name</span>
-{| class="wikitable"
-!Lane||Sample||Enzyme1||Enzyme2
-|-
-|1||100bp ladder||--||--
-|-
-|2||apt12_1R (pSB1C3)-1||--||--
-|-
-|3||apt12_1R (pSB1C3)-2||--||--
-|-
-|4||pT181 antisense(pSB1C3)-1||--||--
-|-
-|5||pT181 antisense(pSB1C3)-2||--||--
-|-
-|6||pT181 antisense(pSB1C3)-3||--||--
-|-
-|7||pT181 antisense(pSB1C3)-4||--||--
-|-
-|8||100bp ladder||--||--
-|}
-[[File:igku_xx.xxx]]<br>
-</div>
-{| class="wikitable"
-!Lane||Sample||Enzyme1||Enzyme2
-|-
-|1||100bp ladder||--||--
-|-
-|2||apt12_1R-DT-1||--||--
-|-
-|3||apt12_1R-DT-2||--||--
-|-
-|4||apt12_1R-DT-3||--||--
-|-
-|5||apt12_1R-DT-4||--||--
-|-
-|6||pT181 attenuator(pSB1C3)-1||--||--
-|-
-|7||pT181 attenuator(pSB1C3)-2||--||--
-|-
-|8||RBS-lysis1-DT-1||--||--
-|-
-|9||RBS-lysis1-DT-2||--||--
-|-
-|10||100bp ladder||--||--
-|}
-[[File:igku_xx.xxx]]<br>
-</div>
-{| class="wikitable"
-!Lane||Sample||Enzyme1||Enzyme2
-|-
-|1||100bp ladder||--||--
-|-
-|2||RBS-lysis2-DT-1||--||--
-|-
-|3||RBS-lysis2-DT-2||--||--
-|-
-|4||RBS-lysis2-DT-3||--||--
-|-
-|5||RBS-lysis2-DT-4||--||--
-|-
-|6||RBS-lysis3-DT-1||--||--
-|-
-|7||RBS-lysis3-DT-2||--||--
-|-
-|8||100bp ladder||--||--
-|}
-[[File:igku_xx.xxx]]<br>
 </div>
@@ Line 263: / Line 209: @@
 |9/5 Ptet+pT181 antisense||2||20||22||--
 |-
-|9/5 Plux+pT181 attenuater||2||20||22||--
+|9/5 Plux+pT181 attenuator||2||20||22||--
 |-
-|9/5 Ptet+pT181 attenuater||2||20||22||--
+|9/5 Ptet+pT181 attenuator||2||20||22||--
 |-
-|9/5 Ptet+pT181 attenuater||2||20||22||--
+|9/5 Ptet+pT181 attenuator||2||20||22||--
 |-
 |9/5 Pconst+RBS-tetR+DT||2||20||22||--
@@ Line 280: / Line 226: @@
 <span class="author">No name</span>
 {| class="wikitable"
-! ||9/5 Pbad/araC||E||S||X||P||BSA||Buffer||MilliQ||total
+! ||9/5 Pbad/araC||EcoRI||SpeI||XbaI||PstI||BSA||Buffer||MilliQ||total
 |-
 |2 cuts||4&micro;L|| 0&micro;L|| 1&micro;L|| 0&micro;L|| 1&micro;L|| 3&micro;L|| 3&micro;L|| 18&micro;L|| 30&micro;L
 |}
 {| class="wikitable"
-! ||9/5 RBS-luxI-DT||E||S||X||P||BSA||Buffer||MilliQ||total
+! ||9/5 RBS-luxI-DT||EcoRI||SpeI||XbaI||PstI||BSA||Buffer||MilliQ||total
 |-
 |2 cuts||4&micro;L|| 0&micro;L|| 0&micro;L|| 1&micro;L|| 1&micro;L|| 3&micro;L|| 3&micro;L||18&micro;L|| 30&micro;L
 |}
 {| class="wikitable"
-! ||8/28 Plux||E||S||X||P||BSA||Buffer||MilliQ||total
+! ||8/28 Plux||EcoRI||SpeI||XbaI||PstI||BSA||Buffer||MilliQ||total
 |-
 |2 cuts|| 12&micro;L|| 0&micro;L|| 1&micro;L|| 0&micro;L|| 1&micro;L|| 3&micro;L|| 3&micro;L||10&micro;L||30&micro;L
@@ Line 297: / Line 243: @@
 |}
 {| class="wikitable"
-! ||9/5 Pconst(J23100)||E||S||X||P||BSA||Buffer||MilliQ||total
+! ||9/5 Pconst(J23100)||EcoRI||SpeI||XbaI||PstI||BSA||Buffer||MilliQ||total
 |-
 |2 cuts||5.7&micro;L||0&micro;L||1&micro;L||0&micro;L||1&micro;L||3&micro;L||3&micro;L||16.3&micro;L||30&micro;L
@@ Line 304: / Line 250: @@
 |}
 {| class="wikitable"
-! ||9/5 Plac||E||S||X||P||BSA||Buffer||MilliQ||total
+! ||9/5 Plac||EcoRI||SpeI||XbaI||PstI||BSA||Buffer||MilliQ||total
 |-
 |2 cuts||6.0&micro;L||0&micro;L||1&micro;L||0&micro;L||1&micro;L||3&micro;L||3&micro;L||16&micro;L||30&micro;L
@@ Line 311: / Line 257: @@
 |}
 {| class="wikitable"
-! ||8/31 Plux-RBS-GFP-DT-1||E||S||X||P||BSA||Buffer||MilliQ||total
+! ||8/31 Plux-RBS-GFP-DT-1||EcoRI||SpeI||XbaI||PstI||BSA||Buffer||MilliQ||total
 |-
 |2 cuts||9.4&micro;L||1&micro;L||1&micro;L||0&micro;L||0&micro;L||3&micro;L||3&micro;L||12.6&micro;L||30&micro;L
@@ Line 318: / Line 264: @@
 |}
 {| class="wikitable"
-! ||8/20 Pconst-RBS-luxR-DT||E||S||X||P||BSA||Buffer||MilliQ||total
+! ||8/20 Pconst-RBS-luxR-DT||EcoRI||SpeI||XbaI||PstI||BSA||Buffer||MilliQ||total
 |-
 |2 cuts||4.5&micro;L||1&micro;L||0&micro;L||1&micro;L||0&micro;L||3&micro;L||3&micro;L||13.5&micro;L||30&micro;L
@@ Line 337: / Line 283: @@
 <div class="experiment">
 <span class="author">No name</span>
+{| class="wikitable"
+!Lane||Sample||Enzyme1||Enzyme2
+|-
+|1||100bp ladder||--||--
+|-
+|2||aptamer 12_1R (pSB1C3)-1||--||--
+|-
+|3||aptamer 12_1R (pSB1C3)-2||--||--
+|-
+|4||pT181 antisense(pSB1C3)-1||--||--
+|-
+|5||pT181 antisense(pSB1C3)-2||--||--
+|-
+|6||pT181 antisense(pSB1C3)-3||--||--
+|-
+|7||pT181 antisense(pSB1C3)-4||--||--
+|-
+|8||100bp ladder||--||--
+|}
+[[File:Igku Sep5 Electrophoresis(N4).jpg]]<br>
+{| class="wikitable"
+!Lane||Sample||Enzyme1||Enzyme2
+|-
+|1||100bp ladder||--||--
+|-
+|2||aptamer 12_1R-DT-1||--||--
+|-
+|3||aptamer 12_1R-DT-2||--||--
+|-
+|4||aptamer 12_1R-DT-3||--||--
+|-
+|5||aptamer 12_1R-DT-4||--||--
+|-
+|6||pT181 attenuator(pSB1C3)-1||--||--
+|-
+|7||pT181 attenuator(pSB1C3)-2||--||--
+|-
+|8||RBS-lysis1-DT-1||--||--
+|-
+|9||RBS-lysis1-DT-2||--||--
+|-
+|10||100bp ladder||--||--
+|}
+[[File:Igku Sep5 Electrophoresis(N6) 2.jpg]]<br>
+{| class="wikitable"
+!Lane||Sample||Enzyme1||Enzyme2
+|-
+|1||100bp ladder||--||--
+|-
+|2||RBS-lysis2-DT-1||--||--
+|-
+|3||RBS-lysis2-DT-2||--||--
+|-
+|4||RBS-lysis2-DT-3||--||--
+|-
+|5||RBS-lysis2-DT-4||--||--
+|-
+|6||RBS-lysis3-DT-1||--||--
+|-
+|7||RBS-lysis3-DT-2||--||--
+|-
+|8||100bp ladder||--||--
+|}
+[[File:Igku Sep5 Electrophoresis(N5).jpg]]<br>
 {| class="wikitable"
 !Lane||Sample||Enzyme1||Enzyme2
@@ Line 344: / Line 354: @@
 |2||Pconst||SpeI||PstI
 |-
-|3||Pconst||--||--
+|3||Pconst NC||--||--
 |-
 |4||Plac||SpeI||PstI
 |-
-|5||Plac||--||--
+|5||Plac NC||--||--
 |-
 |6||Plux||SpeI||PstI
 |-
-|7||Plux||--||--
+|7||Plux NC||--||--
 |-
 |8||Pconst-RBS-luxR-DT||EcoRI||XbaI
 |-
-|9||Pconst-RBS-luxR-DT||--||--
+|9||Pconst-RBS-luxR-DT NC||--||--
 |-
 |10||Plux-RBS-GFP-DT||EcoRI||SpeI
 |-
-|11||Plux-RBS-GFP-DT||--||--
+|11||Plux-RBS-GFP-DT NC||--||--
 |-
 |12||1kbp ladder||--||--
 |}
-[[File:igku_xx.xxx]]<br>
+[[File:Igku Sep5 Electrophoresis(N6) 3.jpg]]<br>
 </div>
-===5*M9(EDTA)===
+===5x M9 Medium (+EDTA)===
 <div class="experiment">
 <span class="author">Hirano</span>
@@ Line 381: / Line 391: @@
 |NH4Cl||10mg
 |-
-|Fe(3)-EDTA||1263.27mg
+|Fe(III)-EDTA||1263.27mg
+|-
+|MilliQ||up to 10 mL
 |}
+*autoclave at 121 &deg;C for 20 min
 </div>
-&deg;C 20minute autoclave
 ===Gel Extraction===
@@ Line 398: / Line 410: @@
 |3||Pconst||SpeI & PstI
 |}
-[[File:igku_xxbeforexx.xxx]]<br>
+[[File:igku_Sep5_gel_extraction_N7_1.jpg]]<br>
-[[File:igku_xxafterxx.xxx]]<br>
+[[File:igku_Sep5_gel_extraction_N7_2.jpg]]<br>
 {| class="wikitable"
 !Name||concentration[&micro;g/mL]||260/280||260/230
@@ Line 418: / Line 430: @@
 |6||Plux||SpeI & PstI
 |}
-[[File:igku_xxbeforexx.xxx]]<br>
+[[File:igku_Sep5_gel_extraction_N7_3.jpg]]<br>
-[[File:igku_xxafterxx.xxx]]<br>
+[[File:igku_Sep5_gel_extraction_N7_4.jpg]]<br>
 {| class="wikitable"
 !Name||concentration[&micro;g/mL]||260/280||260/230
@@ Line 440: / Line 452: @@
 |6||Plux-RBS-GFP-DT||EcoRI & SpeI
 |}
-[[File:igku_xxbeforexx.xxx]]<br>
+[[File:igku_Sep5_gel_extraction_N7_5.jpg]]<br>
-[[File:igku_xxafterxx.xxx]]<br>
+[[File:igku_Sep5_gel_extraction_N7_6.jpg]]<br>
 {| class="wikitable"
 !Name||concentration[&micro;g/mL]||260/280||260/230
@@ Line 449: / Line 461: @@
 |Plux-RBS-GFP-DT (EcoRI & SpeI)||21.8||1.87||0.98
 |}
+===DNA Purification===
+<div class="experiment">
+<span class="author">No name</span>
+{|class="wikitable"
+!DNA||concentration[&micro;g/mL]||260/280||260/230
+|-
+|9/5 RBS-luxI-DT||7.6||1.56||-1.42
+|-
+|9/5 Pbad/araC||7.5||1.54||3.84
+|}
+</div>
 ===Miniprep===
@@ Line 482: / Line 506: @@
 |94&deg;C||94&deg;C||55&deg;C||68&deg;C||--
 |-
-|5m||30s||30s||1m 25s||30cycles
+|5min||30s||30s||1min 25s||30cycles
 |}
-</div>
-===Electrophoresis===
-<div class="experiment">
-<span class="author">No name</span>
-{| class="wikitable"
-!Lane||Sample||Enzyme1||Enzyme2
-|-
-|1||100bp ladder||--||--
-|-
-|2||RBS-lysis3-DT-3||--||--
-|-
-|3||RBS-lysis3-DT-4||--||--
-|-
-|4||RBS-lysis3-DT-5||--||--
-|-
-|5||RBS-lysis1-DT-3||--||--
-|-
-|6||Ptrc KaiC-1||--||--
-|-
-|7||pSB4K5||--||--
-|-
-|8||100bp ladder||--||--
-|}
-[[File:igku_xxxxxx.xxx]]<br>
 </div>
@@ Line 517: / Line 516: @@
 !Sample||medium
 |-
-|9/4 apt12_1R-DT-1||Plusgrow medium
+|9/4 aptamer 12_1R-DT-1||Plusgrow medium (+CP)
+|-
+|9/4 pT181 attenuator(pSB1C3)-1||Plusgrow medium (+CP)
+|-
+|9/4 RBS-lysis2-DT-1||Plusgrow medium (+CP)
 |-
-|9/4 pT181 attenuator(pSB1C3)-1||Plusgrow medium
+|9/4 Ptrc-KaiC -1||Plusgrow medium (+Amp)
 |-
-|9/4 RBS-lysis2-DT-1||Plusgrow medium
+|9/4 pSB4K5 -1||Plusgrow medium (+Kan)
 |}
 </div>

Template:Kyoto/Notebook/Sep 5

From 2013.igem.org

Latest revision as of 14:20, 27 September 2013

Contents

Sep 5

Electrophoresis

Miniprep

Ligation

Electrophoresis

Gel Extraction

Colony PCR

Liquid Culture

Transformation

Restriction Enzyme Digestion

Electrophoresis

5x M9 Medium (+EDTA)

Gel Extraction

DNA Purification

Miniprep

Colony PCR

Liquid Culture