Exeter/29 July 2013

From 2013.igem.org

(Difference between revisions)
(Liquid cultures)
(Digest)
Line 1: Line 1:
-
== Digest ==
 
-
We followed advice from a PhD student and did:
 
-
 
-
* Positive controls of:
 
-
 
-
- RFP cut with E and S
 
-
 
-
- RFP cut with X and P
 
-
 
-
 
-
* Negative control of:
 
-
 
-
- Just water
 
-
 
-
 
-
The buffer and BSA were vortexed before use to make sure they were completely defrosted.
 
-
 
-
We got fresh purite water each time we needed it.
 
-
 
-
We incubated at 37°C for 30 minutes and at 80°C for 20 minutes.
 

Revision as of 11:43, 6 August 2013