Melbourne/Protocols for Standard Methods
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| - | [[Melbourne|<Back to team home page>]] [[ | + | [[Melbourne|<Back to team home page>]] [[Melbourne/Protocol Name:T|<Template>]] |
=Protocol:= | =Protocol:= | ||
| - | *[[ | + | *[[Melbourne/Ligation Protocol|Ligation]] |
| - | *[[ | + | *[[Melbourne/Transformation Protocol|Transformation]] |
| - | *Loading DNA Gel | + | **[[Melbourne/Transformation Protocol shorter|shorter time transformation]] |
| - | * | + | **[[Melbourne/Transformation Protocol re-transformation|re-transformation]] |
| + | *[[Melbourne/Growing up cells|Growing up cells]] | ||
| + | *[[Melbourne/Miniprep protocol|Miniprep protocol]] | ||
| + | *[[Alkaline Lysis Miniprep protocol]] | ||
| + | *[[Melbourne/Diagnostic Digest|Diagnostic Digest]] | ||
| + | *[[Melbourne/Preparing an agarose gel|Preparing an agarose gel]] | ||
| + | *[[Melbourne/Loading a DNA gel|Loading and running a DNA Gel]] | ||
| + | *[[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/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
