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作 者:毛倩倩[1] 周灵[2,3] 唐青海[1] 卜宾 唐存多[1] 焦铸锦[1] 姚伦广[1] 阚云超[1] 杨建伟[1] 崔尚金[3]
机构地区:[1]南阳师范学院,南阳市兽医生物工程技术研究中心,河南省伏牛山昆虫生物学重点实验室,昆虫生物反应器河南省工程实验室,南阳473061 [2]吉林农业大学动物科学技术学院,长春130118 [3]中国农业科学院北京畜牧兽医研究所,北京100193
出 处:《中国畜牧兽医》2016年第7期1659-1666,共8页China Animal Husbandry & Veterinary Medicine
基 金:河南省重点科技攻关项目(142102110101);河南省高等学校重点科研项目(16A230023);南阳师范学院引进人才专项项目(70640)
摘 要:试验旨在制备犬细小病毒(canine parvovirus,CPV)VP2蛋白多克隆抗体。构建pET28a-CPV-VP2重组表达质粒转化大肠杆菌BL21(DE3)感受态细胞,经IPTG诱导,SDS-PAGE鉴定融合蛋白的表达,纯化目的蛋白与佐剂混合、乳化制备后作为免疫原,免疫家兔制备VP2蛋白多克隆抗体;采用免疫过氧化物酶单层细胞染色法(immunoperoxidase monolayer assay,IPMA)检测抗体的免疫活性、抗体滴度、病毒滴度及中和活性。结果表明,重组VP2蛋白(rVP2)以包涵体形式存在,分子质量约为72ku;所制备的多克隆抗体滴度为1 600倍,病毒滴度为107 TCID50/mL,中和效价为1∶2 884,该抗体与体外培养的CPV呈特异性反应,CPV VP2蛋白的多克隆抗体免疫活性和特异性良好,且中和活性高,为CPV基因工程疫苗的研究和临床治疗奠定了基础。This study was aimed to prepare canine parvovirus (CPV)VP2 protein polyclonal anti-body.The recombinant expression vector pET28a-CPV-VP2 was constructed and transfromed into E.coli BL21 (DE3),the expression of recombinant proteins was induced by IPTG from which the fusion protein was identified by SDS-PAGE.The target protein was purified and emulsify with ad-j uvant,the prepared immunogen was inoculated into rabbit by subcutaneous inj ections to prepare of VP2 protein specific polyclonal antibody.The immuno-activity,titers,neutralization titers of the prepared polyclonal antibody were determined by immunoperoxidase monolayer assay (IPMA).The results showed that the expressed recombinant protein VP2 (rVP2)existed in the form of inclusion body with a molecular weight of 72 ku.The prepared polyclonal antibody titer was 1 600 dilution,the virus titer was 107 TCID50/mL,the neutralizing titer was 1∶2 884.The antibodies showed specific reaction with CPV.In conclusion,rVP2 specific polyclonal antibody showed wonderful immunocompetence,specificity and neutralizing activity,providing foundation for the development of genetic vaccine and clinical therapeutic method.
分 类 号:S852.655[农业科学—基础兽医学]
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