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鸡传染性贫血病毒vp3基因的原核表达及其免疫学活性分析
引用本文:陆桂丽,王笑梅,高玉龙,高宏雷,祁小乐,王晓燕. 鸡传染性贫血病毒vp3基因的原核表达及其免疫学活性分析[J]. 中国预防兽医学报, 2006, 28(6): 650-652
作者姓名:陆桂丽  王笑梅  高玉龙  高宏雷  祁小乐  王晓燕
作者单位:1. 中国农业科学院哈尔滨兽医研究所,兽医生物技术国家重点实验室,黑龙江,哈尔滨,150001;新疆农业大学,动物医学院,新疆,乌鲁木齐,830052
2. 中国农业科学院哈尔滨兽医研究所,兽医生物技术国家重点实验室,黑龙江,哈尔滨,150001
摘    要:将鸡传染性贫血病毒(CIAV)Vp3基因克隆入表达载体pET-28a中,然后转化大肠杆菌DH5α,经IPTG诱导,vp3基因以融合蛋白的形式高效表达。SDS-PAGE分析显示,表达的重组蛋白分子量约为18Ku。Westernblot分析表明,该蛋白可与CIAV阳性血清特异性反应。

关 键 词:鸡传染性贫血病毒  vp3基因  原核表达
文章编号:1008-0589(2006)06-0650-03
收稿时间:2005-10-09
修稿时间:2005-10-09

Expression of chicken infectious anemia virus vp3 gene in Escherichia coli and analysis of immunological activity
LU Gui-li,WANG Xiao-mei,GAO Yu-long,GAO Hong-lei,QI Xiao-le,WANG Xiao-yan. Expression of chicken infectious anemia virus vp3 gene in Escherichia coli and analysis of immunological activity[J]. Chinese Journal of Preventive Veterinary Medicine, 2006, 28(6): 650-652
Authors:LU Gui-li  WANG Xiao-mei  GAO Yu-long  GAO Hong-lei  QI Xiao-le  WANG Xiao-yan
Abstract:Chicken infectious anemia virus vp3 gene was cloned into an expression vector pET-28a.The resulting recombinant plasmid was named pET-28a-vp3.A His-tagged recombinant protein was expressed with high efficiency in E.coli transformed by pET-28a-vp3 after induction with IPTG.The fusion protein has an apparent molecular weight of about 18 Ku as indicated by SDS-PAGE analysis,and showed specific reaction with positive serum of CIAV in Western blot.
Keywords:chicken infectious anemia virus  vp3 gene  prokaryotic expression
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