猪繁殖与呼吸综合征病毒糖蛋白2a的原核表达及多克隆抗体制备OA
Prokaryotic expression of glycoprotein 2a of PRRSV and preparation of its polyclonal antibody
为制备抗PRRSV 糖蛋白 2a(Glycoprotein 2a,GP2a)的多克隆抗体,以高致病型XH-GD毒株基因组为模板,通过原核系统表达重组GP2a蛋白.将纯化的重组蛋白免疫兔,获得兔源多克隆抗体,并检测其效价与特异性.结果显示,所得多克隆抗体效价为 1∶12 800,且可与真核表达的Flag-GP2a蛋白发生特异性反应,表明原核表达的GP2a蛋白免疫原性良好,所获抗体效价较高、特异性强,为后续研究GP2a功能奠定了相关基础.
To generate polyclonal antibodies against Glycoprotein 2a(GP2a)of Porcine Reproductive and Respiratory Syndrome Virus(PRRSV),the recombinant GP2a protein was expressed in a prokaryotic system using the genome of the highly pathogenic XH-GD strain as a template.The purified recombinant GP2a was used to immunize rabbits to produce rabbit polyclonal antibodies.The antiserum was subsequently evaluated for its titer and specificity.The results showed that the obtained polyclonal antibodies had a titer of 1∶12,800 and could specifically react with eukaryotic-expressed Flag-GP2a.This indicates that the prokaryotically expressed recombinant GP2a protein possesses good immunogenicity,and the resulting antibodies exhibit high titer and desirable specificity.These findings lay a material foundation for further investigation into the function of PRRSV GP2a.
丘智恒;辛宁;霍展棠;刘栩沂;马春全;陈耀
佛山大学动物科技学院,广东 佛山 528225佛山大学动物科技学院,广东 佛山 528225佛山大学动物科技学院,广东 佛山 528225佛山大学动物科技学院,广东 佛山 528225佛山大学动物科技学院,广东 佛山 528225佛山大学动物科技学院,广东 佛山 528225
农业科技
PRRSV糖蛋白 2a原核表达多克隆抗体
PRRSVGP2aprokaryotic expressionpolyclonal antibody
《佛山科学技术学院学报(自然科学版)》 2026 (1)
8-14,7
广东省基础与应用基础研究项目(2019A1515110056)
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