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Today we ran a sample of our recently (10/20) extracted DNA on an agarose gel in order to ensure the presence of sufficient DNA of at least satisfactory quality. Unfortunately, it appears that the gel preparation was not of optimal quality, but despite this, it appears that we have DNA. We also made a plan for next time and how we are going to adjust the PCR for optimized results. Namely, we will refine the gradient slightly from 42º-61º to 42º-59º.