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Hii, I am currently using RIPA buffer for the extraction of proteins from neuronal cells. But, getting very faint bands on the blot. Initially, I was doubtful about reagents and the protocol...
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In my lab,we are trying to construct a control plasmid. So we have to remove the insert gene which has two restriction ends:one is XhoI and other one is Hind III.So after double digestion we want...
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