| In this paper,a primer was designed and synthesized based on the sequence of the nucleocapsid(H)protein genes of peste des petits ruminants virus(PPRV),which is added BamH I sites for amplifiting the Full-length fragment of the H gene from recombinant plasmids named p TOP-H using PCR.The fragment was cloned into pGM-T vector and transformed into E.coli TOP10,DNA sequence was determined.Then the cloned fragment was subcloned into prokaryotic expression vector pET-32a(+),and the recombinant expression plasmids were expressed in E.coli BL21(DE3) with inducement.The size of the recombinant fusion protein was 80ku(H) analysised by SDS-PAGE.The western-blotting results indicated that the expressed protein can be recognized by the PPRV positive serum. |