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作 者:尚继军[1] 项金忠[1] 谢云[1] 张国强 冯素英 张鹏飞[1]
出 处:《中国生物制品学杂志》1997年第4期196-199,共4页Chinese Journal of Biologicals
摘 要:从乙肝阳性人血清中克隆HBV含前s区表面抗原基因(PreSZ+S),将其插入到杆状病毒转移质粒PVL1393中,并与昆虫病毒ACNPVDNA共转染Sf9昆虫细胞,筛选出重组病毒。用乙肝放免(RIA)试剂盒及EIAPreS2-Ag检测试剂盒检测重组病毒感染的Sf9细胞,表明细胞中有HBsAg及PreS2-Ag存在。将重组病毒感染的细胞免疫小鼠,在小鼠血清中能检测到anti-HBsAg及anti-PreS2抗体。HBV DNA was extracted from HBsAg positive serum and used for the amplication of the whole gene coding HBV surface antigen middle protein by PCR. The gene was inserted into a baculovirus transfer vector pVL1393 and cotransfected into Sf9 insect cells with wild AcNPV DNA,then recombinant virus was screened out. By using RIA and EIA kits, HBsAg and PreS2-Ag were detected out in Sf9 cells infected with the recombinant virus,and the corresponding antibodies of them were also detected out in the serum of mice imunized with the cells.
分 类 号:R512.620.3[医药卫生—内科学] R392.11[医药卫生—临床医学]
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