Team:Evry/Interlab Study/08-30-2014
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+ | <h2>Other constructions of the Anderson library of constitutive promoters</h2> | ||
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- | < | + | Transformation plates observation. |
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+ | <a href="https://static.igem.org/mediawiki/2014/f/fa/Transfo29_08.jpg" class="image"> | ||
+ | <img alt="IMAGE" src="https://static.igem.org/mediawiki/2014/f/fa/Transfo29_08.jpg" width="250px;" class="thumbimage"/> | ||
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+ | <a href="https://static.igem.org/mediawiki/2014/f/fa/Transfo29_08.jpg" class="internal" title="Enlarge"> | ||
+ | <img src="/wiki/skins/common/images/magnify-clip.png" width="15" height="11" alt="Symbol"/> | ||
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+ | <center> Colony number according to plasmid including promoters.</center> | ||
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+ | PCR colony were performed on 8 colonies per transformation plate. PCR products were loaded on 1% agarose gel and gel ran one 45 minutes. There were nothing on gel, reason is probably a mix and temperature problem. | ||
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<span class="cd-date">Aug 30</span> | <span class="cd-date">Aug 30</span> | ||
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Latest revision as of 01:52, 20 September 2014
Other constructions of the Anderson library of constitutive promoters
Transformation plates observation. PCR colony were performed on 8 colonies per transformation plate. PCR products were loaded on 1% agarose gel and gel ran one 45 minutes. There were nothing on gel, reason is probably a mix and temperature problem.
Aug 30