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猪细小病毒SH-1株VP2和NS1基因的克隆与原核表达
引用本文:张春玲,张婉华,臧克伟,邹勇,李春华,蒋凤英,何锡忠,王英.猪细小病毒SH-1株VP2和NS1基因的克隆与原核表达[J].中国动物检疫,2007,24(9):23-25.
作者姓名:张春玲  张婉华  臧克伟  邹勇  李春华  蒋凤英  何锡忠  王英
作者单位:1. 上海农科院畜牧兽医研究所,201106
2. 山东农业大学,山东泰安,271018
摘    要:通过PCR技术,从感染了猪细小病毒的ST细胞中扩增出猪细小病毒的VP2基因和NS1基因,并将其亚克隆至原核表达载体中,分别构建了重组表达载体pET32c/VP2和pET30a/NS1,经IPTG诱导,使pET32c/VP2和pET30a/NS1在受体菌BL21(DE3)中得到高效表达。经Western-blot检测具有生物学活性,为猪细小病毒野毒与疫苗毒的鉴别诊断奠定基础。

关 键 词:猪细小病毒  表达
文章编号:1005-944X(2007)09-0023-03

Molecular Cloning and Prokaryotic Expression of VP2 and NS1 Gene of Porcine Parvovirus SH Strain
ZHANG chunling,ZHANG wanhu,ZANG kewei,ZOU yong,LI chuhu,JIANG fengying,HE xizhong,WANG ying.Molecular Cloning and Prokaryotic Expression of VP2 and NS1 Gene of Porcine Parvovirus SH Strain[J].China Journal Of Animal Quarantine,2007,24(9):23-25.
Authors:ZHANG chunling  ZHANG wanhu  ZANG kewei  ZOU yong  LI chuhu  JIANG fengying  HE xizhong  WANG ying
Institution:1.Animal Husbandry and Veterinary Researy Institute, shanghai Academy of Agricultural Sciences, Shanghai 201106; 2.College of Veterinary Medicine,shangdong Agricultural University, Taian 271018
Abstract:In this study , the open reading frame of PPV VP2 and NS1 were amplified by PCR method from the PPV infected ST cells. Then the products were cloned in prokaryotic vector and pET32c/VP2 and pET30a/NS1expressed were construed respectively .The plasmids were introduced into E. coli BL21. After induction by IPTG , the high expression were found in products of pET32c/VP2 and pET30a/NS1 . Biological activity of the recombinant protein were detected by Western-blot , which can be applied in differential diagnosis of PPV infections.
Keywords:VP2  NS1
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