Team:Evry/Interlab Study/08-30-2014
From 2014.igem.org
(Difference between revisions)
(3 intermediate revisions not shown) | |||
Line 9: | Line 9: | ||
</p> | </p> | ||
- | |||
<br/> | <br/> | ||
+ | <h2>Other constructions of the Anderson library of constitutive promoters</h2> | ||
<br/> | <br/> | ||
- | |||
- | |||
- | |||
- | |||
- | |||
- | |||
- | |||
- | |||
Transformation plates observation. | Transformation plates observation. | ||
<div class="center"> | <div class="center"> | ||
Line 43: | Line 35: | ||
+ | <br/> | ||
<span class="cd-date">Aug 30</span> | <span class="cd-date">Aug 30</span> | ||
</div> | </div> | ||
</div> | </div> | ||
</html> | </html> |
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