摘要
以国内刚刚研制出的PRRSV单克隆抗体为基础,建立了检测PPRS病病毒抗体的单克隆抗体捕获抗原的ELISA法。其单抗包被浓度为1.16μg/mL,粗提病毒反应浓度为16.50μg/mL,血清稀释度为1:40。经与中和试验以及进口ELISA试剂盒比较,证明该法敏感性高,特异性良好.是一种有应用前景的方法。
With monoclonal antibodies (McAb)against PRRSV,a capture ELISA for detecting serum antibodies against PRRSV was developed for the first time. The concentration of coating McAb was 1. 16μg/ml,the reaction concentration of the roughly extracted PRRSV was 16.50μg/ml,and the optimal dilutionrate 0f serum was 1: 40. Compared with the SNT and the ELISA kit from America(Herd Chek,IDEXX),theresult shows that this methord is more sensitive than the others and has a good specificity. It suggests thatthis method will be useful for detecting antibodies against PRRSV in swine sera.
出处
《中国动物检疫》
CAS
2000年第4期24-26,共3页
China Animal Health Inspection