Team:EPF Lausanne/Calendar/17 September 2013

From 2013.igem.org

(Difference between revisions)
 
(2 intermediate revisions not shown)
Line 1: Line 1:
{{Template:EPFL2013Header}}
{{Template:EPFL2013Header}}
-
<font size = "4"> Sensing </font> <BR>
+
<font size = "4"> Cell surface display</font> <BR>
 +
New strategy:
 +
-Dpni digestion of the PCR product, that didn't look perfect on the gel, but might still be worth a try, especially since the time is running out, because the semester starts today.
 +
- Gibson assembly second try of the INP-YFP-Streptavidin construct and the INP-Streptavidin-YFP construct.
 +
<font size = "4"> Sensing-Effector </font> <BR>
-
''Innoculation and glycerol stock'' <BR>
+
''Inoculation and glycerol stock'' <BR>
-
-In the morning I innoculated the bacteria that were grown over night (with the hya-promoter, the cad-prmoter and the constitutive promoter). In the evening I then used this liquid cultures to do a glycerol stock of each construct as well as a MiniPrep of the remaining culture in order to have a plasmid stock.
+
-In the morning I inoculated the bacteria that were grown over night (with the hya-promoter, the cad-prmoter and the constitutive promoter). In the evening I then used this liquid cultures to do a glycerol stock of each construct as well as a MiniPrep of the remaining culture in order to have a plasmid stock.
{{Template:EPFL2013Footer}}
{{Template:EPFL2013Footer}}

Latest revision as of 22:49, 4 October 2013

Taxi.Coli: Smart Drug Delivery iGEM EPFL

Header

Cell surface display
New strategy: -Dpni digestion of the PCR product, that didn't look perfect on the gel, but might still be worth a try, especially since the time is running out, because the semester starts today. - Gibson assembly second try of the INP-YFP-Streptavidin construct and the INP-Streptavidin-YFP construct. Sensing-Effector

Inoculation and glycerol stock
-In the morning I inoculated the bacteria that were grown over night (with the hya-promoter, the cad-prmoter and the constitutive promoter). In the evening I then used this liquid cultures to do a glycerol stock of each construct as well as a MiniPrep of the remaining culture in order to have a plasmid stock.