Melbourne/Protocols for Standard Methods

From 2007.igem.org

< Melbourne(Difference between revisions)
(Protocol:)
 
(5 intermediate revisions not shown)
Line 4: Line 4:
*[[Melbourne/Transformation Protocol|Transformation]]
*[[Melbourne/Transformation Protocol|Transformation]]
**[[Melbourne/Transformation Protocol shorter|shorter time transformation]]
**[[Melbourne/Transformation Protocol shorter|shorter time transformation]]
 +
**[[Melbourne/Transformation Protocol re-transformation|re-transformation]]
*[[Melbourne/Growing up cells|Growing up cells]]
*[[Melbourne/Growing up cells|Growing up cells]]
*[[Melbourne/Miniprep protocol|Miniprep protocol]]
*[[Melbourne/Miniprep protocol|Miniprep protocol]]
Line 11: Line 12:
*[[Melbourne/Loading a DNA gel|Loading and running a DNA Gel]]
*[[Melbourne/Loading a DNA gel|Loading and running a DNA Gel]]
*[[Melbourne/Site directed mutagenesis|Site directed mutagenesis]]
*[[Melbourne/Site directed mutagenesis|Site directed mutagenesis]]
-
*Loading Protein Gel (SDS PAGE)
+
*[[Melbourne/SDS PAGE|SDS PAGE]]
 +
*[[Melbourne/Preparing a poly-acrylamide gel|Preparing a polyacrylamide gel]]
 +
*[[Melbourne/Preparing Protein Samples for SDS PAGEl|Preparing Protein Samples for SDS PAGE]]
 +
*[[Melbourne/DNA concentration measurement|DNA concentration measurement]]
 +
*[[Melbourne/Making glycerol Stocksl|Making Glycerol Stocks]]
 +
*[[Melbourne/Colony PCRl|Colony PCR]]

Latest revision as of 10:03, 8 October 2007

<Back to team home page> <Template>

Protocol: