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A型塞内卡病毒VP1蛋白的原核表达及多克隆抗体制备

秦文珍 于海 单同领 童光志 兰道亮 孔宁 李挺 赵欣 董苏洁 翟焕杰 叶晨倩 叶曼青 童武 郑浩

中国动物传染病学报2024,Vol.32Issue(2):195-200,6.
中国动物传染病学报2024,Vol.32Issue(2):195-200,6.

A型塞内卡病毒VP1蛋白的原核表达及多克隆抗体制备

Prokaryotic Expression of VP1 Protein of Senecavirus A and Preparation of Its Polyclonal Antibodies

秦文珍 1于海 2单同领 2童光志 2兰道亮 3孔宁 2李挺 1赵欣 1董苏洁 2翟焕杰 2叶晨倩 2叶曼青 2童武 2郑浩2

作者信息

  • 1. 西南民族大学畜牧兽医学院,成都 610041||中国农业科学院上海兽医研究所,上海 200241
  • 2. 中国农业科学院上海兽医研究所,上海 200241
  • 3. 西南民族大学畜牧兽医学院,成都 610041
  • 折叠

摘要

Abstract

Senecavirus A(SVA)is an emerging swine pathogen that can cause vesicular lesions in sows and acute death of piglets.In this study,the VP1 gene of SVA was cloned into the prokaryotic expression vectors pCold-Ⅰ and pCold-TF and then the recombinant plasmids VP1-pCold-Ⅰ and VP1-pCold-TF were verified and transformed into E.coli BL21(DE3)to induce the expression of recombinant protein.The results showed that VP1-pCold-Ⅰ existed in the precipitates(inclusion bodies)and VP1-pCold-TF was a soluble protein.The purified proteins were used to immunize BALB/c mice.The polyclonal antibodies were obtained after immunization four times and detected in Western blotting and indirect immunofluorescence assay(IFA).The prepared polyclonal antibodies had good tiers in Western blot and IFA,which provided a tool for relevant basic and applied research.

关键词

A型塞内卡病毒/VP1/原核表达/多克隆抗体

Key words

Senecavirus A/VP1/prokaryotic expression/polyclonal antibody

分类

农业科技

引用本文复制引用

秦文珍,于海,单同领,童光志,兰道亮,孔宁,李挺,赵欣,董苏洁,翟焕杰,叶晨倩,叶曼青,童武,郑浩..A型塞内卡病毒VP1蛋白的原核表达及多克隆抗体制备[J].中国动物传染病学报,2024,32(2):195-200,6.

基金项目

西南民族大学中央高校基本科研业务费专项资金项目(2020YYXS70) (2020YYXS70)

中国动物传染病学报

OA北大核心CSTPCD

1674-6422

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