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乙型肝炎病毒前S2基因克隆及真核表达载体的构建
引用本文:魏中南,夏剑波.乙型肝炎病毒前S2基因克隆及真核表达载体的构建[J].微循环学杂志,2011,21(1):19-20,80,84.
作者姓名:魏中南  夏剑波
作者单位:湖北省妇幼保健院检验科,武汉,430070
摘    要:目的:克隆乙型肝炎病毒前S2基因,构建其真核表达质粒.方法:以乙型肝炎患者血清HBV DNA为模板,设计引物扩增全长前S2基因,再将目的基因插入到真核载体pcDNA3.1(+)中,经PCR、酶切和DNA测序确认.结果:从患者血清抽提的DNA中扩增得到约860bp大小的目的片段,经回收、纯化、酶切后转化大肠杆菌DH5α,...

关 键 词:乙型肝炎病毒  前S2基因  克隆  真核表达

Cloning of Hepatitis B Virus PreS2 Gene and Construction of Eukaryotic Expression Vector
Wei Zhongnan,Xia Jianbo.Cloning of Hepatitis B Virus PreS2 Gene and Construction of Eukaryotic Expression Vector[J].Chinese Journal of Microcirculation,2011,21(1):19-20,80,84.
Authors:Wei Zhongnan  Xia Jianbo
Institution:Wei Zhongnan,Xia Jianbo/Department of Clinical Laboratory,Hubei Maternal and Child Health Hospital,Wuhan 430070
Abstract:Objective:To clone HBV preS2 gene and construct an eukaryotic expressive vector pcDNA-S2.Method:HBV preS2 gene was amplified by PCR from serum of a chronic HBV carrier,and cloned into the eukaryotic vector pcDNA3.1(+),then authenticated by PCR,digestive enzymes and sequencing.Results:A 860bp fragment of the preS2 gene was successfully amplified by PCR from the serum,and inserted into the eukaryotic vector pcDNA3.1(+). The positive clone was identified by PCR,enzyme digestion and DNA sequencing.Conclusion:Eu...
Keywords:Hepatitis B virus  PreS2 gene  Clone  Eukaryotic expression  
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