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水貂肠炎病毒VP2基因的原核表达及多克隆抗体的制备

卞赛赛 梁琳 高窦 周灵 李沛然 杨双双 雷程红 崔尚金 刘维全

中国兽医科学2017,Vol.47Issue(5):597-602,6.
中国兽医科学2017,Vol.47Issue(5):597-602,6.DOI:10.16656/j.issn.1673-4696.2017.05.011

水貂肠炎病毒VP2基因的原核表达及多克隆抗体的制备

Prokaryotic expression of VP2 gene of mink enteritis virus and preparation of anti-serum

卞赛赛 1梁琳 2高窦 3周灵 2李沛然 1杨双双 2雷程红 3崔尚金 2刘维全3

作者信息

  • 1. 新疆农业大学动物医学学院,新疆乌鲁木齐830052
  • 2. 中国农业科学院北京畜牧兽医研究所,北京100193
  • 3. 中国农业大学生物学院,北京100193
  • 折叠

摘要

Abstract

The study aims to express the capsid protein VP2 of mink parvovirus in Escherichia coli(E.coli) and prepare its anti-serum.At first,according to the sequence of VP2 gene,two specific primers were designed.The recombinant plasmid pB-MEV-L with full length MEV genome was used as template in PCR amplification.After insertion of VP2 gene into prokaryotic expression vector pET-32a,the recombinant plasmid pET-MEV-VP2 was constructed successfully.Then transformation of pET-MEV-VP2 into E.coli BL21(DE3) and high expression was induced by IPTG.After 4 times immunization with the purified VP2 protein,the antiserum titer for ELISA was 1:1 024.The result of immunofluorescence assay showed that the rabbit antiserum had a good combined activity.All the results laid a solid foundation for further study of the biological characteristics of MEV.

关键词

水貂肠炎病毒/VP2/原核表达/抗血清

Key words

mink enteritis virus/VP2/prokaryotic expression/antiserum

分类

农业科技

引用本文复制引用

卞赛赛,梁琳,高窦,周灵,李沛然,杨双双,雷程红,崔尚金,刘维全..水貂肠炎病毒VP2基因的原核表达及多克隆抗体的制备[J].中国兽医科学,2017,47(5):597-602,6.

基金项目

国家高技术研究发展计划(863)项目(2011AA10A213) (863)

中国农业科学院创新工程项目(ASTIP-IAS15) (ASTIP-IAS15)

中国兽医科学

OA北大核心CSCDCSTPCD

1673-4696

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