摘要
本研究初步建立了检测AEV抗体的单抗捕捉ELISA 方法。AEV腹水单抗(腹水效价为1 ∶1×106)最佳稀释度为1∶200,AEV抗原工作浓度为16.08 μg/mL,血清稀释度为1∶1 00, 兔抗鸡酶标抗体工作浓度为1∶500。经阻断试验、交叉试验、重复试验,以及与进口试剂 盒 进行平行检测40份血清,总符合率为92.5%,表明该方法特异性强、重复性好、敏感性高, 是一种有应用前景的方法。
: The procedure of capture ELISA for detection of AEV an tibodies were e stablished with the monoclonal antibodies against AEV, and the best concentratio ns of the monoclonal antibodies, the AEV and HRP-Rabbit antichichen were 1/200 , 16.08 μg/mL, and 1/500 respectively.The good stability of capture ELISA were v er ified by inhibited tests, cross tests , reproducible tests,parallel tests with E LISA kit from America (IDEXX).
出处
《动物医学进展》
CSCD
2002年第1期72-75,共4页
Progress In Veterinary Medicine
基金
山东省农科院青年基金支持项目