This week we electrophoresis of DNAs obtained from the PCR to last week. We prepare Cuba's 20 x 40, the gel (acrylamide, ethylene glycol, tristaurina EDTA buffer, free water, ammonium persulfate and fear), then sow the samples (DNAs results of the 3 types of different DNA extraction, 2 normal heteroduplex between patient and normal) and let it run 24 hours. Next week I will reveal and analyze the results.
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