Team:Panama/7 June 2011

From 2011.igem.org

(Difference between revisions)
(Created page with "we prepared:  500ml LB medium  Autoclaving LB medium  Glycerol 30% for preservation  Check the medium with plasmids, colonies grows well; negative control doesn’t ...")
 
Line 1: Line 1:
-
we prepared:
+
We prepared:
 +
 
 500ml LB medium
 500ml LB medium
 +
 Autoclaving LB medium
 Autoclaving LB medium
-
 Glycerol 30% for preservation  
+
 
 +
 Glycerol 30% for preservation
 +
 Check the medium with plasmids, colonies grows well; negative control doesn’t grow after 22h on incubation.
 Check the medium with plasmids, colonies grows well; negative control doesn’t grow after 22h on incubation.
 +
 We inoculate bacterias with plasmids P+R, R+T and with Rh in liquid LB + Amp. Incubate at 37oC in shaker.
 We inoculate bacterias with plasmids P+R, R+T and with Rh in liquid LB + Amp. Incubate at 37oC in shaker.

Latest revision as of 04:24, 29 September 2011

We prepared:

 500ml LB medium

 Autoclaving LB medium

 Glycerol 30% for preservation

 Check the medium with plasmids, colonies grows well; negative control doesn’t grow after 22h on incubation.

 We inoculate bacterias with plasmids P+R, R+T and with Rh in liquid LB + Amp. Incubate at 37oC in shaker.