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I tried a pH of Tris 8.8 pH but after TEV cleavage, I find there is less cleavage and not much desired protein. Which buffer should be used so that no changes in between would be done to prevent...
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Am getting a chaperone at around 63 kD . I have my construct in pETM41. Am purifying with amylose resin and getting a chaperone after affinity. Will HIC after first step clean my protein?
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