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猪脑心肌炎病毒GXLC株VP1基因的原核表达及鉴定
引用本文:李向涛,施开创,陈宏备,郑敏,钟诚,李军.猪脑心肌炎病毒GXLC株VP1基因的原核表达及鉴定[J].动物医学进展,2011,32(2):6-9.
作者姓名:李向涛  施开创  陈宏备  郑敏  钟诚  李军
作者单位:广西大学动物科学技术学院;广西动物疫病预防控制中心;
基金项目:广西科学基金项目(桂科青0728047); 广西科技创新能力与条件建设基金项目(08-05-01D)
摘    要:根据猪脑心肌炎病毒(EMCV)GXLC株的基因组序列设计一对特异性引物,应用RT-PCR方法扩增EMCV VPl基因目的片段,将其克隆至原核表达载体pET-32a(+),构建了EMCV VPl基因重组表达质粒pET-32a-VP1.将pET-32a-VP1转化BL21(DE3)株感受态细胞,并用IPTG进行诱导表达.结...

关 键 词:脑心肌炎病毒  VP1基因  原核表达  抗原性  

Prokaryotic Expression and Identification of VP1 Gene of Encephalomyocarditis Virus GXLC Strain from Swine
LI Xiang-tao,SHI Kai-chuang,CHEN Hong-bei,ZHENG Min,ZHONG Cheng,LI Jun.Prokaryotic Expression and Identification of VP1 Gene of Encephalomyocarditis Virus GXLC Strain from Swine[J].Progress In Veterinary Medicine,2011,32(2):6-9.
Authors:LI Xiang-tao  SHI Kai-chuang  CHEN Hong-bei  ZHENG Min  ZHONG Cheng  LI Jun
Institution:LI Xiang-tao1,SHI Kai-chuang2,CHEN Hong-bei1,ZHENG Min2,ZHONG Cheng1,LI Jun2(1.College of Animal Science and Technology,Guangxi University,Nanning,Guangxi,530005,China,2.Guangxi Center for Animal Disease Control and Prevention,530001,China)
Abstract:One pair of primers were designed according to the genomic sequence of porcine encephalomyocarditis virus(EMCV)GXLC strain,and the VP1 gene was amplified by RT-PCR.The target fragment was cloned into prokaryotic expression vector pET-32a(+) to construct a recombinant expression vector pET-32a-VP1.Then,the pET-32a-VP1 plasmid was transformed into E.coli BL21(DE3)strain and induced by IPTG to produce recombinant VP1 protein.The results of SDS-PAGE analysis showed that the recombinant VP1 protein was efficient...
Keywords:Encephalomyocarditis virus  VP1 gene  prokaryotic expression  antigenicity  swine  
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