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Hello everybody, I have been expressing proteins that contain disulfide bridges and I usually use pET32 which cantains Trx as chaperone and Rosetta gami as strain. This system works for some...
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I treated Ni-NTA column with 10% APS because I purified a protein using a buffer containing DTT and it tourned brown. After APS treatment I wash the column with water and then I stripped it with...
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