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作 者:蔡方舟 陈倩 佟巍 李丹 王卫 CAI Fangzhou;CHEN Qian;TONG Wei;LI Dan;WANG Wei(Institute of Laboratory Animal Sciences,Chinese Academy of Medical Sciences(CAMS),Comparative Medicine Center,Peking Union Medical College(PUMC),Beijing Key Laboratory for Animal Models of Emerging and Reemerging Infectious Diseases,NHC Key Laboratory of Human Disease Comparative Medicine,Beijing 100021,China)
机构地区:[1]中国医学科学院医学实验动物研究所北京协和医学院比较医学中心新发再发传染病动物模型研究北京市重点实验室国家卫生健康委员会人类疾病比较医学重点实验室
出 处:《中国比较医学杂志》2019年第11期85-90,共6页Chinese Journal of Comparative Medicine
基 金:中央级公益性科研院所基本科研业务费课题(2018JT35001);国家传染病重大专项课题(2017ZX10304402-001)
摘 要:目的 建立小鼠抗狂犬病毒Ig G抗体ELISA检测方法,用于狂犬病小鼠模型的检测和分析。方法通过正交实验确定样品最佳稀释度和二抗最佳浓度等工作条件;并对该方法的特异性、灵敏性、稳定性等进行分析;与商品化试剂盒一同用于小鼠样品的检测,确定该ELISA方法的符合率。结果 该ELISA方法的样品最佳稀释度是1∶100,二抗最佳浓度是40 ng/m L,阳性临界值为0. 121。该ELISA方法与小鼠常见病毒阳性血清无交叉反应;检测浓度下限为129μg/m L;样本三次重复的变异系数小于10%。与商品化试剂盒的符合率为100%。结论成功建立小鼠抗狂犬病毒Ig G抗体ELISA检测方法,可应用于狂犬病小鼠模型的分析以及疫苗效价的评估工作中。Objective To establish an ELISA assay for the detection of mouse IgG antibody to rabies virus. Methods Orthogonal experiments were used to determine the optimal dilution of the sample and optimal concentration of the secondary antibody. The stability, specificity and sensitivity test of the assay was determined. The assay result of these samples were compared with those of a commercial kit. Results The optimal dilution of the sample was 1∶100, the optimal concentration of the secondary antibody was 40 ng/ mL, and the cutoff value was 0. 121. There was no crossover with the common mouse viruses, and the minimum detection sensitivity was 129 μg/ mL, and the coefficient variation of the three replicates of the sample was less than 10%. The coincidence rate with the commercial kit was 100%. Conclusions An ELISA assay for the detection of a mouse IgG antibody to rabies virus was successfully established, which can be used for detection and analysis of rabies mouse models.
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