Team:Paris-Saclay/Project/Notebook/Week 4

From 2012.igem.org

(Difference between revisions)
Line 28: Line 28:
<a href="https://2012.igem.org/Team:Paris-Saclay/Project/Abstract">
<a href="https://2012.igem.org/Team:Paris-Saclay/Project/Abstract">
<div class="child-tile"><p class="child-tile">GEMOTE Project</p></div>
<div class="child-tile"><p class="child-tile">GEMOTE Project</p></div>
-
             <img src="http://www.igem-paris-saclay.u-psud.fr/wordpress/wp-content/uploads/2012/07/Aud.jpg" alt="" />
+
             <img src="https://static.igem.org/mediawiki/2012/7/7c/Project-1.png" alt="" />
</a>
</a>
         </div>
         </div>
<div>
<div>
<a href="https://2012.igem.org/Team:Paris-Saclay/Project/Abstract">
<a href="https://2012.igem.org/Team:Paris-Saclay/Project/Abstract">
-
<img src="http://www.ecole-adn.fr/uploads/2011/09/Probiotics-300x300.jpg" alt="" />
+
<img src="https://static.igem.org/mediawiki/2012/d/d1/Project2.jpg" alt="" />
<div class="child-tile"><p class="child-tile">GEMOTE Project</p></div>
<div class="child-tile"><p class="child-tile">GEMOTE Project</p></div>
</a>
</a>

Revision as of 22:23, 26 September 2012

Follow us !

Week 4

  • We place an order for the primers
  • DNA (biobricks) Resuspension using iGEM protocol
  • Transformation of each biobricks by thermal shock to have a large quantity of DNA
  • Staggering of the transformed bacteria on a selective medium to select bacteria which received the plasmid
  • We put some colonies, for each biobricks, on liquid culture to be able to make a Miniprep
  • Miniprep to purify each biobrick (ready to use)
  • Groove for two colonies because they did not grown on the liquid culture