Imperial College/1 September 2008
From 2008.igem.org
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| 1 || 1050 || 0.054 || 0.003 || Y || | | 1 || 1050 || 0.054 || 0.003 || Y || | ||
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- | | 2 || 1145 || 0.062 || 0.008 || Y || 10<sup>4-6</sup> | + | | 2 || 1145 || 0.062 || 0.008 || Y || 10<sup>4-6</sup>x |
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| 4 || 1340 || 0.531 || 0.066 || N || | | 4 || 1340 || 0.531 || 0.066 || N || | ||
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- | | 8 || 1745 || 1.390 || 0.232 || Y || 10<sup>6-8</sup> | + | | 8 || 1745 || 1.390 || 0.232 || Y || 10<sup>6-8</sup>x |
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- | | 24 || 1000 || 1.762 || 0.305 || Y || 10<sup>5-9</sup> | + | | 24 || 1000 || 1.762 || 0.305 || Y || 10<sup>5-9</sup>x |
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Revision as of 13:33, 2 September 2008
Wet LabWe carried out a PCR experiment in an attempt to clone genes (such as EpsE, AmyE integration sites etc.) from vectors. However, due to problems with the image viewer, we did not manage to take an image of the gel by the end of the day. Cloning
Growth CurveThe illuminator's software is not sensitive enough to detect colonies accurately to count them. We have decided to count colonies manually instead. Results from the growth curve trial are shown below:
DebriefingToday we had an extensive debreifing session, the notes below summaries the key points:
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