Team:EPF Lausanne/Calendar/30 July 2013

From 2013.igem.org

(Difference between revisions)
Line 3: Line 3:
''Streptavidin'' <BR>
''Streptavidin'' <BR>
-
Inoculation of the pET21a Streptavidin Dead we received in 3ml LB + Amp, we incubated them for 8h to make a glycerol Stock. <BR>
+
-Inoculation of the pET21a Streptavidin Dead we received in 3ml LB + Amp, we incubated them for 8h to make a glycerol Stock. <BR>
-
Inoculation of the pET21a Streptavidin Dead we received in 3ml LB + Amp, overnight (16hrs) to make a miniprep the day after.  
+
-Inoculation of the pET21a Streptavidin Dead we received in 3ml LB + Amp, overnight (16hrs) to make a miniprep the day after.  
-
<br> We did the ''final PCR'' of ''pINP_construct'' with the following optimal condititons: volume 50µl, 76°C, 5% DMSO.
+
<br> -We did the ''final PCR'' of ''pINP_construct'' with the following optimal condititons: volume 50µl, 76°C, 5% DMSO.
-
<br> We did a 0.8% electrophoresis gel to verify the PCR product.  
+
<br> -We did a 0.8% electrophoresis gel to verify the PCR product.  
{{Template:EPFL2013Footer}}
{{Template:EPFL2013Footer}}

Revision as of 14:35, 3 October 2013

Taxi.Coli: Smart Drug Delivery iGEM EPFL

Header

Cell Surface Display

Streptavidin
-Inoculation of the pET21a Streptavidin Dead we received in 3ml LB + Amp, we incubated them for 8h to make a glycerol Stock.
-Inoculation of the pET21a Streptavidin Dead we received in 3ml LB + Amp, overnight (16hrs) to make a miniprep the day after.
-We did the final PCR of pINP_construct with the following optimal condititons: volume 50µl, 76°C, 5% DMSO.
-We did a 0.8% electrophoresis gel to verify the PCR product.