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>
-
<h2>Contruction n°1: PSB1C3 with I20260</h2>
 
<br/>
<br/>
 +
<h2>Other constructions of the Anderson library of constitutive promoters</h2>
<br/>
<br/>
-
<br/><h2>Contruction n°2: PSB1C3 with J23101-E1010</h2>
 
-
<br/>
 
-
 
-
<br/>
 
-
<br/><h2> Contruction n°3: PSB1C3 with K823012-E1010</h2>
 
-
<br/>
 
-
 
-
<h2>Constructions with other promoters</h2>
 
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

Picture


Other constructions of the Anderson library of constitutive promoters


Transformation plates observation.
IMAGE
Colony number according to plasmid including promoters.
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