Template:Kyoto/Notebook/Aug 28
From 2013.igem.org
(Difference between revisions)
(→Colony PCR) |
(→Liquid Culture) |
||
(6 intermediate revisions not shown) | |||
Line 171: | Line 171: | ||
|4||8/17 RBS-GFP-DT-(2)||--||-- | |4||8/17 RBS-GFP-DT-(2)||--||-- | ||
|- | |- | ||
- | |5||8/20 Pcon-RBS-GFP-DT-(1)||EcoRI|| | + | |5||8/20 Pcon-RBS-GFP-DT-(1)||EcoRI||SpeI |
|- | |- | ||
|6||8/20 Pcon-RBS-GFP-DT-(1)||--||-- | |6||8/20 Pcon-RBS-GFP-DT-(1)||--||-- | ||
Line 189: | Line 189: | ||
|13||8/20 RBS-tetR-DT||--||-- | |13||8/20 RBS-tetR-DT||--||-- | ||
|} | |} | ||
- | [[File: | + | [[File:Igku Aug28 Electrophoresis(ColoP)(N4)pic.jpg]]<br> |
</div> | </div> | ||
Line 211: | Line 211: | ||
|} | |} | ||
[[File:Igku Aug28 Gel Extraction(N⑤-1,2)before.jpg]]<br> | [[File:Igku Aug28 Gel Extraction(N⑤-1,2)before.jpg]]<br> | ||
- | [[File: | + | [[File:Igku Aug28 Gel Extraction4-2.jpg]]<br> |
{| class="wikitable" | {| class="wikitable" | ||
!Lane||DNA||Enzyme | !Lane||DNA||Enzyme | ||
Line 272: | Line 272: | ||
!|Sample||base pair | !|Sample||base pair | ||
|- | |- | ||
- | |8/27 Pλ-luxI-1|| | + | |8/27 Pλ-luxI-1||-- |
|- | |- | ||
- | |8/27 Pλ-luxI|| | + | |8/27 Pλ-luxI||-- |
|} | |} | ||
{| class="wikitable" | {| class="wikitable" | ||
Line 283: | Line 283: | ||
|5min||30s||30s||30min||3cycles | |5min||30s||30s||30min||3cycles | ||
|} | |} | ||
- | [[File: | + | [[File:Igku Aug28 ColonyPCR(N⑦-2).jpg]] |
</div> | </div> | ||
Line 311: | Line 311: | ||
|5min||30s||30s||48s||30cycles | |5min||30s||30s||48s||30cycles | ||
|} | |} | ||
- | |||
===Liquid Culture=== | ===Liquid Culture=== | ||
Line 323: | Line 322: | ||
|J23100 Master Plate-1||Plusgrow medium(+Amp) | |J23100 Master Plate-1||Plusgrow medium(+Amp) | ||
|- | |- | ||
- | |Plac Master Plate-1||Plusgrow medium(+CP) | + | |Plac Master Plate-1||Plusgrow medium(+CP) |
|} | |} | ||
</div> | </div> | ||
Line 358: | Line 357: | ||
|8/26 Pλ-RBS-luxI-DT-1||Plusgrow medium (+Amp) | |8/26 Pλ-RBS-luxI-DT-1||Plusgrow medium (+Amp) | ||
|- | |- | ||
- | |8/26 Pλ-RBS-luxI-DT-2||Plusgrow medium (+Amp) | + | |8/26 Pλ-RBS-luxI-DT-2||Plusgrow medium (+Amp) |
|} | |} | ||
* incubate 37°C 10hour | * incubate 37°C 10hour | ||
</div> | </div> |
Latest revision as of 03:46, 28 September 2013
Contents |
Aug 28
Electrophoresis
Miniprep
DNA | concentration[µg/mL] | 260/280 | 260/230 |
---|---|---|---|
8/27 Plux | 173.8 | 1.95 | 1.45 |
Ligation
state | Vector | Inserter | ||
---|---|---|---|---|
experiment | 8/17 DT-1 | 3.0 | 8.0 |
- Samples were evaporeted used evaporator into about 3 µL.
sample | MilliQ | Ligation High | total |
---|---|---|---|
3 | 4 | 3.5 | 10.5 |
- incubate one hour at 16 °C
Gel Extraction
Lane | DNA |
---|---|
1 | 100bpladder |
3 | SasA(8/27 Genome PCR production) |
5 | RpaA(8/27 Genome PCR production) |
7 | RpaB(8/27 Genome PCR production) |
9 | PkaiBC(8/27 Genome PCR production) |
Name | concentration[µg/mL] | 260/280 | 260/230 |
---|---|---|---|
RpaA | 15.4 | 1.88 | 0.03 |
SasA | 21.6 | 1.66 | 0.79 |
PkaiBC | 16.3 | 1.79 | 0.68 |
RpaB | 26.7 | 1.77 | 0.82 |
Colony PCR
Sample | base pair |
---|---|
8/21 RBS-lysis2-(3) | 772 |
8/21 RBS-lysis2-(4) | 772 |
8/21 RBS-lysis2-(5) | 772 |
8/21 RBS-lysis2-(6) | 772 |
PreDenature | Denature | Annealing | Extension | cycle |
---|---|---|---|---|
94°C | 94°C | 55°C | 68°C | -- |
5min | 30s | 30s | 48s | 30cycles |
Restriction Enzyme Digestion
8/22 RBS-lysis1-(1) | EcoRI | SpeI | BufferB | BSA | MilliQ | total | |
---|---|---|---|---|---|---|---|
2 cuts | 9µL | 0.5µL | 0.5µL | 3µL | 0.3µL | 16.7µL | 30µL |
NC | 1µL | 0µL | 0µL | 1µL | 0.1µL | 7.9µL | 10µL |
8/17 RBS-GFP-DT-(2) | XbaI | PstI | BufferD | BSA | MilliQ | total | |
---|---|---|---|---|---|---|---|
2 cuts | 4µL | 0.5µL | 0.5µL | 3µL | 0.3µL | 21.7µL | 30µL |
NC | 0.5µL | 0µL | 0µL | 1µL | 0.1µL | 8.4µL | 10µL |
8/20 Pcon-RBS-GFP-DT-(1) | EcoRI | SpeI | BufferB | BSA | MilliQ | total | |
---|---|---|---|---|---|---|---|
2 cuts | 3µL | 0.5µL | 0.5µL | 3µL | 0.3µL | 22.7µL | 30µL |
NC | 0.3µL | 0µL | 0µL | 1µL | 0.1µL | 8.6µL | 10µL |
8/20 Pcon-RBS-luxR-DT-(1) | EcoRI | XbaI | BufferD | BSA | MilliQ | total | |
---|---|---|---|---|---|---|---|
2 cuts | 2µL | 0.5µL | 0.5µL | 3µL | 0.3µL | 23.7µL | 30µL |
NC | 0.3µL | 0µL | 0µL | 1µL | 0.1µL | 8.6µL | 10µL |
8/28 Plux | SpeI | PstI | BufferD | BSA | MilliQ | total | |
---|---|---|---|---|---|---|---|
2 cuts | 6µL | 0.5µL | 0.5µL | 3µL | 0.3µL | 19.7µL | 30µL |
NC | 1µL | 0µL | 0µL | 1µL | 0.1µL | 7.9µL | 10µL |
8/20 RBS-tetR-DT-(1) | XbaI | PstI | BufferD | BSA | MilliQ | total | |
---|---|---|---|---|---|---|---|
2 cuts | 5µL | 0.5µL | 0.5µL | 3µL | 0.3µL | 20.7µL | 30µL |
NC | 0.5µL | 0µL | 0µL | 1µL | 0.1µL | 8.4µL | 10µL |
- incubated 37°C 1hour
Electrophoresis
Lane | Sample | Enzyme1 | Enzyme2 |
---|---|---|---|
1 | 8/22 RBS-lysis1-(1) | EcoRI | SpeI |
2 | 8/22 RBS-lysis1-(1) | -- | -- |
3 | 8/17 RBS-GFP-DT-(2) | XbaI | PstI |
4 | 8/17 RBS-GFP-DT-(2) | -- | -- |
5 | 8/20 Pcon-RBS-GFP-DT-(1) | EcoRI | SpeI |
6 | 8/20 Pcon-RBS-GFP-DT-(1) | -- | -- |
7 | 100bp ladder | -- | -- |
8 | 8/20 Pcon-RBS-luxR-DT-(1) | EcoRI | XbaI |
9 | 8/20 Pcon-RBS-luxR-DT-(1) | -- | -- |
10 | 8/28 Plux | SpeI | PstI |
11 | 8/28 Plux | -- | -- |
12 | 8/20 RBS-tetR-DT | XbaI | PstI |
13 | 8/20 RBS-tetR-DT | -- | -- |
Gel Extraction
Lane | DNA | Enzyme |
---|---|---|
1 | 100bp ladder | -- |
2 | 8/20 RBS-lysis1-(1) | EcoRI & SpeI |
3 | ||
4 | -- | -- |
5 | 8/28 RBS-GFP-DT-(2) | XbaI & PstI |
6 |
Lane | DNA | Enzyme |
---|---|---|
1 | 100bp ladder | -- |
2 | 8/28 Plux | SpeI & PstI |
3 | ||
4 | -- | -- |
5 | 8/20 RBS-tetR-DT-(1) | XbaI & PstI |
6 |
Name | concentration[µg/mL] | 260/280 | 260/230 |
---|---|---|---|
Pcon-RBS-GFP-DT (EcoRI&SpeI) | 7.1 | 1.88 | 0.07 |
Pcon-RBS-luxR-DT (EcoRI&XbaI) | 15.3 | 1.93 | 0.70 |
Plux (SpeI&PstI) | 4.5 | 1.79 | 0.31 |
RBS-GFP-DT (XbaI&PstI) | 6.0 | 2.16 | 0.03 |
RBS-tetR-DT (XbaI&PstI) | 7.6 | 1.91 | 0.38 |
Colony PCR
Sample | base pair |
---|---|
8/27 pT181 attenuator-DT-1 | 738 |
8/27 pT181 attenuator-DT-2 | 738 |
8/27 pT181 attenuator-DT-3 | 738 |
8/27 TetR-aptamer 12_1R-DT-1 | 521 |
8/27 TetR-aptamer 12_1R-DT-2 | 521 |
8/27 pT181 antisense-DT-1 | 542 |
PreDenature | Denature | Annealing | Extension | cycle |
---|---|---|---|---|
94°C | 94°C | 55°C | 68°C | -- |
5min | 30s | 30s | 30s | 30cycles |
Sample | base pair |
---|---|
8/27 Pλ-luxI-1 | -- |
8/27 Pλ-luxI | -- |
PreDenature | Denature | Annealing | Extension | cycle |
---|---|---|---|---|
94°C | 94°C | 55°C | 68°C | -- |
5min | 30s | 30s | 30min | 3cycles |
Colony PCR
No name
Sample | base pair |
---|---|
8/21 RBS-lysis2-9 | 772 |
8/21 RBS-lysis2-10 | 772 |
8/21 RBS-lysis2-11 | 772 |
8/21 RBS-lysis2-12 | 772 |
8/21 RBS-lysis2-13 | 772 |
8/21 RBS-lysis2-14 | 772 |
PreDenature | Denature | Annealing | Extension | cycle |
---|---|---|---|---|
94°C | 94°C | 55°C | 68°C | -- |
5min | 30s | 30s | 48s | 30cycles |
Liquid Culture
Sample | medium |
---|---|
8/16 Master Plate(CP)-6 DT | Plusgrow medium(+CP) |
J23100 Master Plate-1 | Plusgrow medium(+Amp) |
Plac Master Plate-1 | Plusgrow medium(+CP) |
Ligation
state | Vector | Inserter | ||
---|---|---|---|---|
experiment | 8/27 DT (EcoRI & XbaI) | 2.9 | 8/28 RBS-lysis1 (EcoRI & SpeI) | 9.5 |
experiment | 8/28 Plux (SpeI & PstI) | 2.3 | 8/28 RBS-GFP-DT (XbaI & PstI) | 18 |
experiment | 8/28 Pcon-RBS-luxR-DT (EcoRI & XbaI) | 3.3 | 8/28 Pcon^RBS-GFP-DT-(1) (EcoRI & SpeI) | 28 |
experiment | 8/27 DT (EcoRI & XbaI) | 2.7 | 8/24 Spinach (EcoRI & SpeI) | 2.4 |
- Samples were evaporeted used evaporator into about 1 µL.
sample | MilliQ | Ligation High | total |
---|---|---|---|
1 | 3 | 4 | 9 |
- incubate overnight at 4 °C
Liquid Culture
Sample | medium |
---|---|
8/26 Pλ-RBS-luxI-DT-1 | Plusgrow medium (+Amp) |
8/26 Pλ-RBS-luxI-DT-2 | Plusgrow medium (+Amp) |
- incubate 37°C 10hour