Team:EPF Lausanne/Calendar/6 September 2013

From 2013.igem.org

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(Created page with "{{Template:EPFL2013Header}} Sensing <BR> '''PCR of the effector Backbones and the effector insert MMP2 and MMP9 without GFP'' <BR> I did a 50ul PCR reaction of the Backbone and...")
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Sensing <BR>
Sensing <BR>
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'''PCR of the effector Backbones and the effector insert MMP2 and MMP9 without GFP'' <BR>
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'''PCR of the effector Backbones and the effector insert MMP2 and MMP9 without GFP''' <BR>
I did a 50ul PCR reaction of the Backbone and insert of the effector constructs. I again used a program where the first ten cylces are 10C° bellow the norma annealing temperature. The Gel electrophoresis showed that there was some sort of contamination, proably in the Primer Mixes. So I did the primer mixes again.
I did a 50ul PCR reaction of the Backbone and insert of the effector constructs. I again used a program where the first ten cylces are 10C° bellow the norma annealing temperature. The Gel electrophoresis showed that there was some sort of contamination, proably in the Primer Mixes. So I did the primer mixes again.

Revision as of 18:54, 30 September 2013

Taxi.Coli: Smart Drug Delivery iGEM EPFL

Header

Sensing

PCR of the effector Backbones and the effector insert MMP2 and MMP9 without GFP
I did a 50ul PCR reaction of the Backbone and insert of the effector constructs. I again used a program where the first ten cylces are 10C° bellow the norma annealing temperature. The Gel electrophoresis showed that there was some sort of contamination, proably in the Primer Mixes. So I did the primer mixes again.