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伪狂犬病病毒主要抗原表位基因KgE的表达及纯化
引用本文:周松峰,吴健敏,关忠宜,廖文军,白安斌.伪狂犬病病毒主要抗原表位基因KgE的表达及纯化[J].动物医学进展,2011,32(11):6-9.
作者姓名:周松峰  吴健敏  关忠宜  廖文军  白安斌
作者单位:1. 广西大学动物科学技术学院,广西南宁530005;广西兽医研究所,广西南宁530001
2. 广西兽医研究所,广西南宁,530001
基金项目:农业科技跨越计划项目(2009跨21); 广西自然科学基金项目(2011GXNSFA018086)
摘    要:从伪狂犬病病毒(PRV)基因组中克隆出KgE抗原表位基因,并将其插入到原核表达载体pETTrx中,构建了原核表达质粒pET-Trx-KgE,将pET-Trx-KgE转化至BL21 (DE3) plysS中,在IPTG诱导下进行表达.SDS-PAGE分析表明,KgE基因在BL21( DE3) plysS中获得高效表达,表...

关 键 词:伪狂犬病病毒  KgE基因  原核表达

Expression and Purification of Pseudorabies Virus Main Antigen Epitope Gene KgE
ZHOU Song-feng,WU Jian-min,GUAN Zhong-yi,LIAO Wen-jun,BAI An-bin.Expression and Purification of Pseudorabies Virus Main Antigen Epitope Gene KgE[J].Progress In Veterinary Medicine,2011,32(11):6-9.
Authors:ZHOU Song-feng  WU Jian-min  GUAN Zhong-yi  LIAO Wen-jun  BAI An-bin
Institution:ZHOU Song-feng1,2,WU Jian-min2,GUAN Zhong-yi2,LIAO Wen-jun2,BAI An-bin2 (1.College of Animal Sciences and Technology,Guangxi Univeristy,Nanning,Guangxi,530005,China,2.Guangxi Veterinary Research Institute,530001,China)
Abstract:The main antigen epitope gene KgE was cloned from pig pseudorabies virus genome by conventional PCR method and inserted into the prokaryotic expression vector pET-trx,constructed recombinant plasmid pET-Trx-KgE and then transformed into competent cell BL21.The target protein was expressed with IPDG induction and obtained a high level expression by SDS-PAGE analysis,it took possession of whole bacterial proteins about 32.8% and presented as inclusion bodies mainly with weight 36 ku.The purity of expressed pr...
Keywords:Pseudorabies virus  KgE gene  prokaryotic expression  
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