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- W2357830263 abstract "Based on the analysis of the amino acid sequences of envelope protein E of duck Tembusu virus( DTMUV) strain( JS804) by bioinformatics software,eight peptides with good antigenicity were linked cloned into T vector,then the gene( named TEM) was accurately cloned into plasmid p ET32 a. The correct recombinant plasmid p ET32a-TEM was transferred into competent Escherichia coli BL21 cells and the recombinant protein was induced and expressed with isopropyl thiogalactoside( IPTG). SDS-PAGE showed that the fusion protein was 38 000 in size and existed in the form of insoluble inclusion body. Western blotting analysis and mouse immunological results revealed the good specificity of the fusion protein. The successful expression of mass-peptide will lay the foundations for the development of serological diagnosis and effective bioengineering vaccines for duck Tembusu virus detection." @default.
- W2357830263 created "2016-06-24" @default.
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- W2357830263 date "2015-01-01" @default.
- W2357830263 modified "2023-09-28" @default.
- W2357830263 title "Coexpression and antigenicity of epitopes on duck Tembusu virus envelope protein E" @default.
- W2357830263 hasPublicationYear "2015" @default.
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