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伪狂犬病病毒UL36蛋白单克隆抗体的制备和鉴定

陈玲超 孔宁 于海 单同领 童光志 郑浩 王兴娅 李俊波 李佳佳 王晨 李松楠 王安铖 孟鑫 童武

中国兽医科学2024,Vol.54Issue(3):373-378,6.
中国兽医科学2024,Vol.54Issue(3):373-378,6.DOI:10.16656/j.issn.1673-4696.2024.0038

伪狂犬病病毒UL36蛋白单克隆抗体的制备和鉴定

Preparation and identification of monoclonal antibody against pseudorabies virus UL36 protein

陈玲超 1孔宁 1于海 1单同领 1童光志 1郑浩 1王兴娅 2李俊波 3李佳佳 4王晨 1李松楠 1王安铖 2孟鑫 3童武1

作者信息

  • 1. 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||安徽农业大学生命科学院,安徽合肥 230036
  • 3. 中国农业科学院上海兽医研究所,上海 200241||东北林业大学野生动物学院,黑龙江哈尔滨 150040
  • 4. 中国农业科学院上海兽医研究所,上海 200241||安徽农业大学动物科技学院,安徽合肥 230036
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摘要

Abstract

VP1/2,a tegument protein encoded by the pseudorabies virus UL36 gene,plays an important role in the assembly of virions.In this study,UL36 gene was mainly used as the research object,the truncated UL36 gene was cloned into pCold I vector to construct the recombination prokaryotic expression plasmid pCold I-UL36.After induced expression,the recombinant protein expressed in inclusion body form was denatured,affinity chromatography and renaturation to obtain high purity protein.Then,BALB/c mice were immunized with purified protein.A hybridoma cell strain named UL36-6,stably secreting antibodies against UL36 was obtained by cell fusion and indirect ELISA screening.The identification of antibody subtype showed that it was IgG1 and κ.The ascites antibody had high neutralization titer and purity.The Western-blot and indirect immunofluorescence test results showed that the monoclonal antibody had good specificity.In conclusion,we successfully prepared a monoclonal antibody against PRV UL36 protein in the present study which will lay a foundation for further study of the biological function of UL36 protein.

关键词

伪狂犬病病毒/UL36基因/VP1/2/单克隆抗体

Key words

pseudorabies virus/UL36gene/VP1/2/monoclonal antibody

分类

农业科技

引用本文复制引用

陈玲超,孔宁,于海,单同领,童光志,郑浩,王兴娅,李俊波,李佳佳,王晨,李松楠,王安铖,孟鑫,童武..伪狂犬病病毒UL36蛋白单克隆抗体的制备和鉴定[J].中国兽医科学,2024,54(3):373-378,6.

基金项目

上海市科技创新行动计划项目(20392002500) (20392002500)

中国兽医科学

OA北大核心CSTPCD

1673-4696

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