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猪胸膜肺炎放线杆菌间接ELISA检测方法的建立 被引量:2

Establishment of Indirect ELISA for Porcine Actinobacillus pleuropneumoniae
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摘要 用纯化的重组蛋白抗原作为ELISA包被抗原,通过对抗原包被浓度、血清稀释倍数、酶标二抗稀释倍数、抗原和血清反应时间、血清和酶标二抗反应时间、显色剂作用时间和中止液滴加量的优化,建立了检测胸膜肺炎放线杆菌抗体的间接ELISA方法。特异性实验证明该ELISA方法特异性较强。将建立的ELISA方法与IDEXX公司的标准试剂盒进行了比较,二者的符合率较高,说明建立的ELISA方法比较敏感,为ELISA检测方法的商品化奠定了基础。 Using the purified protein antigen as the coating antigen of ELISA, the optimal conditions of the ELISA including the protein concentration for coating, dilution of serum and conjugate, reaction time of antigen and serum, that of serum and conjugate, reaction time of developer, quantum of stop solution were all determined. Indirect ELISA method detecting App antibody was established at last. The specific character of ELISA method was relative strong by specific test. The coincidence of the established ELISA method and the standard kit of IDEXX were relative high, which indicated that the established ELISA method was rather sensitive. This test has established a foundation for commercialization of detection method of ELISA.
出处 《中国兽药杂志》 2008年第7期1-4,共4页 Chinese Journal of Veterinary Drug
基金 上海市科委科研项目资助 课题编号:027205026
关键词 胸膜肺炎放线杆菌 APXIV 间接ELISA Actinobacillus pleuropneumoniae ApxlV indirect ELISA
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参考文献9

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