Team:Newcastle/Labwork/22 September 2009
From 2009.igem.org
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Today again we redid the digests of the sac miniprep however again there was no DNA present. | Today again we redid the digests of the sac miniprep however again there was no DNA present. | ||
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+ | ==<u> Chassis team </u>== | ||
+ | |||
+ | ===Introduction=== | ||
+ | |||
+ | |||
+ | |||
+ | <br> | ||
+ | |||
+ | ===Experiment procedure=== | ||
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+ | ==== 1 ==== | ||
+ | ==== 2==== | ||
+ | |||
+ | ==== 3 ==== | ||
+ | |||
+ | |||
+ | ===Conclusion=== | ||
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+ | |||
+ | <br> | ||
+ | [[Image:|400px|center]] | ||
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+ | ===Futher plan=== | ||
{{:Team:Newcastle/Project/Labwork/CalTemplate}} | {{:Team:Newcastle/Project/Labwork/CalTemplate}} |
Revision as of 12:41, 20 October 2009
Formal Lab Session - 22nd September 2009
Stochastic switch team
Today we transformed E.coli JM109 cels with the overnight ligation product from yesterday using the promega protocol. We used the following controls:
- Tube 1: Backbone + insert + ligase (proper ligation)
- Tube 2: Backbone + ligase (control for background ligation level)
- Tube 3: Backbone + insert (control for ligase effectiveness)
These were left in the incubator for an hour and then plated out (2 plates per tube 200ul and 50ul) onto Amp + Tet LB plated and put in the 37C incubator overnight.
Today again we redid the digests of the sac miniprep however again there was no DNA present.
Chassis team
Introduction
Experiment procedure
1
2
3
Conclusion
[[Image:|400px|center]]
Futher plan
|
|
|
|
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]