I came across few protocols that suggest dissolving protein in SDS and few in PBS. Just wanted to know the basis..
Hi there,
SDS is a detergent which is denaturing for proteins whereas PBS is a buffer which has no nefast effect on its own on the protein structure.
If the protein pellet comes from inclusion bodies you wont be able to dissolve it in pbs, need a denaturant
Oh! Bunches of thanks for the kind response... So I can store in SDS..
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