Team:Newcastle/Labwork/9 October 2009
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* Prepared our biobricks to send for sequencing. Measured the concentration of the midipreps for our work. | * Prepared our biobricks to send for sequencing. Measured the concentration of the midipreps for our work. | ||
* Diluted the primers for pSB1AT3 | * Diluted the primers for pSB1AT3 | ||
- | * Digest yesterday's Mini prep results | + | * Digest yesterday's Mini prep results |
+ | * Gel extraction for cotC PCR fragment after digestion, 4 sample's from Jen's promoter library experiment. | ||
== Conclusion == | == Conclusion == |
Revision as of 02:17, 21 October 2009
Formal Lab Session - 9th October 2009
Introduction
- Prepared our biobricks to send for sequencing. Measured the concentration of the midipreps for our work.
- Diluted the primers for pSB1AT3
- Digest yesterday's Mini prep results
- Gel extraction for cotC PCR fragment after digestion, 4 sample's from Jen's promoter library experiment.
Conclusion
- The colonies form cotC transformation are right colonies.
- We picked some colonies for kinA transformation growed on LB+Amp plate, after mini prep and digestion, the result of digestion told us that the colonies growed on LB+Amp plate are right colonies. Even they should not grow on LB+Amp plates.
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News
Events
- 20 – 21 June 2009 - Europe workshop (London)
- 23 – 24 June 2009 - UK iGEM meetup (Edinburgh)
- 23 October Practice Presentation (Newcastle)
- 23 October T-shirts are ready
- 27 October Practice Presentation (Sunderland)
- 27 October Poster is ready
- 30 October – 2 November 2009 - Jamboree (Boston)
Social Net
- Newcastle iGEM Twitter
- [http://www.facebook.com/home.php#/group.php?gid=131709337641 Newcastle on Facebook]
- [http://www.youtube.com/user/newcastle2009igem Newcastle Youtube Channel]