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- W2350297908 abstract "To investigate the prokaryotic expression and explore the possibilities as a vaccine candidate antigens of HutB from V.alginolyticus HY9901,the hutB gene was cloned by PCR,and then followed by digestion,connection,the prokaryotic expression vector pET-HutB was constructed through directional inserting into pET-28a(+),then transformed into Escherichia coli BL21(DE3) with IPTG induction.After verification of SDS-PAGE the inducted expression and purification conditions was optimized further.The results showed that:The optimization condition of inducible expression for HutB protein in E.coli was optimazed at 37℃ for 3 hours,with 0.4mmol/L IPTG.The best elution concentration of imidazole was 300mmol/L,and the expressed protein existed in the form of inclusion body.The recombinant HutB fusion protein could be combined with mouse anti-His-Tag antibody." @default.
- W2350297908 created "2016-06-24" @default.
- W2350297908 creator A5090549816 @default.
- W2350297908 date "2014-01-01" @default.
- W2350297908 modified "2023-09-23" @default.
- W2350297908 title "Prokaryotic Expression and Purification of the Recombinant Hemin-Binding Protein(HutB) of Vibrio alginolyticus Strain HY9901" @default.
- W2350297908 hasPublicationYear "2014" @default.
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