PCR Analysis of Tail DNA

Revision as of 16:31, 5 June 2009 by Swat (Talk | contribs)

Revision as of 16:31, 5 June 2009 by Swat (Talk | contribs)

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: .4ul

Reverse Primer: .4ul

dNTPs: .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