Difference between revisions of "Davidson Missouri W/Davidson Protocols"
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'''Web Tools We Use''' | '''Web Tools We Use''' | ||
| + | #[http://gcat.davidson.edu/iGEM08/tools.html All Sites In One Place] | ||
#[http://gcat.davidson.edu/iGEM08/gelwebsite/gelwebsite.html Optimize your Gel] | #[http://gcat.davidson.edu/iGEM08/gelwebsite/gelwebsite.html Optimize your Gel] | ||
#[http://gcat.davidson.edu/iGEM07/genesplitter.html Gene Splitting Web Site] | #[http://gcat.davidson.edu/iGEM07/genesplitter.html Gene Splitting Web Site] | ||
Revision as of 16:09, 11 July 2008
- How to Keep a Lab Notebook
- Common molecular reagents
- Standard Assembly
- BioBrick Ends
- Compatibility of Plasmids
- Building dsDNA with Oligos
- Setting up PCR mixtures
- PCR and Mg2+ concentration
- Clean and Concentrate DNA (after PCR, before digestion)
- Pouring an agarose gel
- Calculate MWs
- Digest DNA with restriction enzymes
- Double Digest Guide
- Ethanol Precipitate DNA (short protocol)
- 1kb MW markers
- Shrimp Alkaline Phosphatase
- Qiagen QIAquick Gel Purification
- Qiagen QIAquick Column Regeneration Protocol
- ElectroElute Gel Purification
- Ligation Protocol
- Heat Shock Transformation OR Short version of Heat Shock
- Zippy Transformation
- Colony PCR to Screen for Successful Ligations
- Promega miniprep
- Choices for Transformation: Heat Shock vs. Zyppy
- Choices for Mini-Preps: Promega vs. Zyppy
- Making dsDNA Using Primer Dimers
Web Tools We Use
