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作 者:谢立[1] 黄德庄[1] 贺立香[1] 罗朝霞[1] 周育森[2]
机构地区:[1]北京市卫生局肝炎研究所 [2]军事医学科学院微生物流行病研究所,北京100071
出 处:《中国病毒学》2005年第4期444-446,共3页Virologica Sinica
摘 要:Amplified HDV fragment by RT-PCR was cloned into T vector and PQE_{31} plasmid, which established a prokaryotic expression vector in E coli M_{15} The recombinant protein was purified by Ni-NTA column affinity chromatography, and identified by Western blot and ELISA: HDV antigen was expressed efficiently and had a well antigenicity character. It can be used in HDV clinical diagnosis and epidemiology survey.Amplified HDV fragment by RT-PCR was cloned into T vector and PQE31 plasmid, which established a prokaryotic expression vector in E coli M15 The recombinant protein was purilied by Ni-NTA column affinity chromatography,and identified by Western blot and ELISA:HDV antigen was expressed efficiently and had a well antigenicity character. It can be used in HDV clinical diagnosis and epidemiology survey.
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