Team:EPF Lausanne/Calendar/25 August 2013

From 2013.igem.org

(Difference between revisions)
 
(6 intermediate revisions not shown)
Line 1: Line 1:
{{Template:EPFL2013Header}}
{{Template:EPFL2013Header}}
 +
<font size = "4"> Cell Surface Display </font>
 +
<br>Planning next experiments.
 +
<br><br>
-
<font size = "4"> Sensing </font> <BR>
+
<font size = "4"> Sensing-Effector </font> <BR>
-
''PCR of Cad Backbone (1.2-B)'' <BR>
+
''PCR of Cad Backbone'' <BR>
-We tried to amplify the Backbone for the Cad-GFP construct. But it did not work. Since the restriction digest implied that the plasmid was correct, the problem must have been with the primer temperatures. So we decided to design new primers and try another PCR with the old ones but also adding DMSO.  
-We tried to amplify the Backbone for the Cad-GFP construct. But it did not work. Since the restriction digest implied that the plasmid was correct, the problem must have been with the primer temperatures. So we decided to design new primers and try another PCR with the old ones but also adding DMSO.  

Latest revision as of 09:49, 4 October 2013

Taxi.Coli: Smart Drug Delivery iGEM EPFL

Header

Cell Surface Display
Planning next experiments.

Sensing-Effector

PCR of Cad Backbone
-We tried to amplify the Backbone for the Cad-GFP construct. But it did not work. Since the restriction digest implied that the plasmid was correct, the problem must have been with the primer temperatures. So we decided to design new primers and try another PCR with the old ones but also adding DMSO.