Team:EPF Lausanne/Calendar/24 July 2013

From 2013.igem.org

(Difference between revisions)
 
(6 intermediate revisions not shown)
Line 1: Line 1:
{{Template:EPFL2013Header}}
{{Template:EPFL2013Header}}
-
'''Cell surface Display'''
+
<font size = "4">Cell Surface Display</font> <BR>
 +
Our Primers arrived today. <BR>
-
''Primers arrived:'' we did a PCR (see protocols) to amplifay ''pINP_construct'' to first remove the EYFP sequence and by the same way add overhangs for the Gibson reaction.
+
''PCR'' <BR>
-
We thus dis a 0.8% Gel electrophoresis to verify the PCR product. The PCR needed to be optimised.
+
We did a PCR (see protocols) to amplify ''pINP_construct'' to first remove the EYFP sequence and by the same way add overhangs for the Gibson reaction.
-
 
+
We thus did a 0.8% Gel electrophoresis to verify the PCR product. The PCR needed to be optimised.
-
'''General'''
+
<BR><BR>
 +
<font size = "4">General</font>
Competent cells try 2.  
Competent cells try 2.  
 +
{{Template:EPFL2013Footer}}
{{Template:EPFL2013Footer}}

Latest revision as of 21:23, 4 October 2013

Taxi.Coli: Smart Drug Delivery iGEM EPFL

Header

Cell Surface Display
Our Primers arrived today.

PCR
We did a PCR (see protocols) to amplify pINP_construct to first remove the EYFP sequence and by the same way add overhangs for the Gibson reaction. We thus did a 0.8% Gel electrophoresis to verify the PCR product. The PCR needed to be optimised.

General

Competent cells try 2.