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- W2374310551 abstract "Objective: To express the recombinant C-terminal of fibrin protein in Escherichia coli,and to investigate the antigenicity.Method: The DNA encoding C-terminal of fibrin protein of egg drop syndrome virus(EDSV) was amplified by PCR,and then cloned into constitutive and secretary plasmid pUC18ompAcat to construct pUC18ompA-EDS.The recombinant plasmid was introduced into E.coli BL21(DE3) to construct engineering bacteria.Result: Recombinant protein could be expressed in engineering bacteria,and partial recom-binant protein was secreted into periplasmic space and culture medium.The recombinant C-terminal of fibrin protein purified by Ni2+-NTA affinity chromatography could react with antiserum of chicken infected with EDSV.Conclusion: The recombinant protein had obvious antigenicity.This study will offer some reference to the production of gene engineering vaccine against EDSV." @default.
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- W2374310551 date "2010-01-01" @default.
- W2374310551 modified "2023-09-26" @default.
- W2374310551 title "Secretary Expression and Antigenicity Analysis of C-terminal of Fibrin Protein on Egg Drop Syndrome Virus" @default.
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