Team:Groningen/Labwork/13 September 2013
From 2013.igem.org
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<br>Plates containing several combination of signal sequences together with S3 or S9 showed colonies. | <br>Plates containing several combination of signal sequences together with S3 or S9 showed colonies. | ||
<br>Colony PCR was performed (NEB Mater Mix) on 2 colonies per plate using VF2 and VR primers (annealing temperature 64°C). | <br>Colony PCR was performed (NEB Mater Mix) on 2 colonies per plate using VF2 and VR primers (annealing temperature 64°C). | ||
- | <br><img src="" width="50%" > | + | <br><img src="https://static.igem.org/mediawiki/2013/4/4d/ColonyPCR-SignalSeq_1.jpg" width="50%" > |
- | <br><img src="" width="50%" > | + | <br><img src="https://static.igem.org/mediawiki/2013/b/b4/ColonyPCR-SignalSeq_2.jpg" width="50%" > |
<h2>Inne</h2> | <h2>Inne</h2> |
Revision as of 13:02, 14 September 2013
Claudio
The plates pSB1C3-S16-3-5 and pSB1C3-S16-9-11 showed around thousands of colonies.Colony PCR was performed (NEB Mater Mix) on 4 colonies per plate using VF2 and VR primers (annealing temperature 64°C).
Colony C from pSB1C3-S16-3-5 and colony D from pSB1C3-S16-9-11 were positive candidate and were inoculated in LB + Cm.
Plates containing several combination of signal sequences together with S3 or S9 showed colonies.
Colony PCR was performed (NEB Mater Mix) on 2 colonies per plate using VF2 and VR primers (annealing temperature 64°C).
Inne
Ran 2 gels with colony pcr samples.Gel 1:
Ladder | s16-3-5 A | s16-3-5 B | s16-3-5 C | s16-3-5 D | s16-9-11 A | s16-9-11 B | s16-9-11 C | s16-9-11 D | Positive control |
Gel 2
Ladder | 1 A | 1 B | empty | empty | 2 A | 2 B | 3 A | 3 B | 4 A | 4 B |
Ladder | 5 A | 5 B | 6 A | 6 B | 7 A | 7 B | 8 A | 8 B | empty | empty |