Team:EPF-Lausanne/Last News

From 2009.igem.org

(Difference between revisions)
Line 3: Line 3:
</div><div CLASS="epfl09">
</div><div CLASS="epfl09">
-
<html>
+
 
<a href="" onMouseOver="document.MyImage.src='https://static.igem.org/mediawiki/2009/1/11/Lov2.png';" onMouseOut="document.MyImage.src='https://static.igem.org/mediawiki/2009/4/42/Lov.png';">
<a href="" onMouseOver="document.MyImage.src='https://static.igem.org/mediawiki/2009/1/11/Lov2.png';" onMouseOut="document.MyImage.src='https://static.igem.org/mediawiki/2009/4/42/Lov.png';">
<img src="https://static.igem.org/mediawiki/2009/4/42/Lov.png" name="MyImage"></a>  
<img src="https://static.igem.org/mediawiki/2009/4/42/Lov.png" name="MyImage"></a>  
-
</html>
+
 

Revision as of 13:16, 29 July 2009

Contents


<a href="" onMouseOver="document.MyImage.src='https://static.igem.org/mediawiki/2009/1/11/Lov2.png';" onMouseOut="document.MyImage.src='https://static.igem.org/mediawiki/2009/4/42/Lov.png';"> <img src="Lov.png" name="MyImage"></a>



Last News




Keep track with what we did so far

(12.07.09)

This first week of wetlab we have done the following things
  • Transformed the plasmids with the LovTAP gene, generously sent by Dr. Sosnick's lab from Chicago universtiy, into competent E.Coli
  • Designed the cloning strategy for cloning the LovTAP gene from its original vector to a iGEM vector+add an inducible promoter (LacI) (+RBS +term.)
  • Ordered and received the primers needed for the PCR of LovTAP
  • Designed the cloning strategy for inclusion of the LovTAP BioBrick with different reporting cassettes
  • Transformed all the BioBricks that will be needed for the cloning strategies (c.f. notebook for more information about these parts) into competent E.Coli
  • Fused the two BioBricks "LacI" and "RBS"
  • Digested the LovTAP PCR products and RBS part