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- W2349025035 abstract "Aim: To express matrix attachment region(MAR) binding protein(MBP) of Dunaliella salina in the prokaryotic expression system.Methods:The MBP gene was amplified by RT-PCR using a pair of primers designed according to the cDNA sequence of MBP gene with specific restriction enzyme sites,followed ligated into the vector pET28(+) to construct a recombinant vector pET-MBP,then transformed into E.coli BL21(DE3) to express the fusion protein with the presence of IPTG.Western blotting was performed to determine the expression of the fusion protein.The protein was purified by Ni2+ affinity chromatography.Results: The results showed that RT-PCR products were about 1 600 bp long,the fusion protein was about 75 000 measured by SDS-PAGE.The fusion proteins accounted for more than 70% of the total protein.Conclusion:The prokaryotic expression vector has been constructed successfully." @default.
- W2349025035 created "2016-06-24" @default.
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- W2349025035 date "2008-01-01" @default.
- W2349025035 modified "2023-09-26" @default.
- W2349025035 title "Cloning and prokaryotic expression of matrix attachment region binding protein gene of Dunaliella salina" @default.
- W2349025035 hasPublicationYear "2008" @default.
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