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- W2389183778 abstract "To produce recombinant human MBD4 protein, the ORF of MBD4 cDNA was inserted into pGEX-6P1 expression vector fused in frame with an upstream GST gene. The expression plasmid was transformed into E.coli BL21(DE3) strain and protein expression was induced by IPTG. The GST-MBD4 fusion protein was purified from cell lysates using glutathione Sepharose 4B affinity chromatography. The GST tag was removed from fusion protein by site-specific Prescision protease cleavage. MBD4 protein was purified through Mono Q anion exchange to more than 94% homogeneity. The purified protein has both methylated DNA binding and DNA glycosylase activity." @default.
- W2389183778 created "2016-06-24" @default.
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- W2389183778 date "2006-01-01" @default.
- W2389183778 modified "2023-09-28" @default.
- W2389183778 title "Purification and Characterization of Recombinant Human MBD4 Protein Expressed in E.coli" @default.
- W2389183778 hasPublicationYear "2006" @default.
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