Melbourne/Protocols for Standard Methods
From 2007.igem.org
< Melbourne(Difference between revisions)
(→Protocol:) |
|||
| (3 intermediate revisions not shown) | |||
| Line 12: | 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]] | ||
| - | * | + | *[[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/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:
- Ligation
- Transformation
- Growing up cells
- Miniprep protocol
- Alkaline Lysis Miniprep protocol
- Diagnostic Digest
- Preparing an agarose gel
- Loading and running a DNA Gel
- Site directed mutagenesis
- SDS PAGE
- Preparing a polyacrylamide gel
- Preparing Protein Samples for SDS PAGE
- DNA concentration measurement
- Making Glycerol Stocks
- Colony PCR
