Team:EPF-Lausanne/Last News

From 2009.igem.org

(Difference between revisions)
Line 5: Line 5:
[[Image:Lov.png|lov]]
[[Image:Lov.png|lov]]
[[Image:Lov2.png|lov2]]
[[Image:Lov2.png|lov2]]
 +
<SCRIPT LANGUAGE="JavaScript">
 +
<!-- Begin
 +
loadImage1 = new Image();
 +
loadImage1.src = "https://static.igem.org/mediawiki/2009/1/11/Lov2.png";
 +
staticImage1 = new Image();
 +
staticImage1.src = "https://static.igem.org/mediawiki/2009/4/42/Lov.png";
 +
 +
// End -->
 +
</script>
 +
 +
<!-- STEP TWO: Insert this code into the BODY of your HTML document  -->
 +
 +
<span onmouseover="image1.src=loadImage1.src;" onmouseout="image1.src=staticImage1.src;">
 +
<img name="image1" src="https://static.igem.org/mediawiki/2009/4/42/Lov.png" border=0></span>
<html><center>
<html><center>

Revision as of 12:41, 29 July 2009

Contents

lov lov2 <SCRIPT LANGUAGE="JavaScript"> </script>


<img name="image1" src="Lov.png" border=0>

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