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I'm purifying a protein which is homotetrameric in nature and each subunit is catalytically active. However, I am a bit uncertain about the molecular weight which I should consider upon...
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Guys, I have a pET vector 30a+ and my gene of interest has been inserted between XhoI and KpnI sites. Nearest to it is only an S-tag present. How can I purify my protein and remove the s-tag from...
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