Difference between revisions of "PCR Analysis of Tail DNA"
From Bridges Lab Protocols
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see [[Preparing an Agarose Gel]] for details on preparing a DNA gel | see [[Preparing an Agarose Gel]] for details on preparing a DNA gel | ||
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Revision as of 14:43, 28 May 2012
see Genotyping Details for strain specific details
Materials
Protocol
Use the following Volumes per Reaction:
- Buffer: 4 uL of 5X Go-Taq buffer ("Molecular Biology Stuff" box in freezer)
- Forward Primer: 0.4ul
- Reverse Primer: 0.4ul
- dNTPs: 0.4uL of 2 mM ("Molecular Biology Stuff" box in freezer)
- Sterile water: 13.6 uL
- Polymerase Go-Taq: 1 uL (6th floor in Genotype Yellow Box in freezer)
- Template: 1 uL
Run PCR Program (approx 2 hours). Use Cycler 1 on 6th Floor
- Login: Sergey, Just press enter to Login
- Under Genotype folder, pick Ingles program for Ingles genotyping
- Under Genotype folder, pick regpcr program for PLT genotyping
Make sure to press enter 2x once to confirm Tubes and second time to start PCR
see Preparing an Agarose Gel for details on preparing a DNA gel
