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Following protease treatment, the histones were dialyzed against buffer D (20 mM sodium acetate pH 5.2, 200 mM NaCl, 5 mM β-mercaptoethanol, 1 mM EDTA, and 6 M urea), and the untagged histone was further purified by Resource S cation exchange column chromatography (Cytiva) using buffer D containing a linear gradient of NaCl from 200 to 900 mM