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作 者:王琴琴 刘博 支德娟[1] 王东升 Wang Qinqin;Liu Bo;Zhi Dejuan;Wang Dongsheng(School of Pharmacy,Lanzhou University,Lanzhou 730000,China)
出 处:《兰州大学学报(医学版)》2023年第1期20-24,31,共6页Journal of Lanzhou University(Medical Sciences)
基 金:甘肃省自然科学基金资助项目(20JR10RA619);国家级大学生创新创业训练计划项目(202110730220)。
摘 要:目的 建立并应用A型肉毒毒素(BoNT/A)含量的ELISA检测方法。方法 采用免疫学技术,制备并纯化了兔源性抗BoNT/A切割突触小体相关蛋白SNAP-25后暴露出的八肽序列SNAP-25 (190-197)特异性抗体,建立BoNT/A含量的ELISA检测方法,且进行方法学验证,完成相关样品检测。结果 成功制备并纯化获得八肽兔多克隆抗体,建立的BoNT/A含量ELISA检测方法具有良好的灵敏度、特异性、重复性、适用性等优点。结论 成功建立了BoNT/A含量的ELISA检测方法,可用于相关样品的BoNT/A含量检测。Objective To establish and apply a detection method of ELISA for the content of botulinum toxin type A(BoNT/A).Methods An antibody against octapeptide(190-197)of synaptosomal-associated protein of 25 kDa(SNAP-25)produced by cleavage with BoNT/A was prepared and purified from rabbit serum.Then,ELISA for the content detection of BoNT/A was built,validated and used to measure the related samples.Results The antibody of octapeptide was successfully obtained and purified from rabbits,and the ELISA of the content detection method for BoNT/A,which was developed in this paper,was sensitive,specific,repeatable and applicable.Conclusion An ELISA of the content detection method for BoNT/A was successfully developed,and can be used to measure the content of BoNT/A in related samples.
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