Team:EPF Lausanne/Calendar/24 July 2013

From 2013.igem.org

(Difference between revisions)
Line 1: Line 1:
{{Template:EPFL2013Header}}
{{Template:EPFL2013Header}}
'''Cell surface Display'''
'''Cell surface Display'''
 +
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 amplifay ''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'''
'''General'''

Revision as of 14:21, 3 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 amplifay 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.