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间接ELISA检测羊伪狂犬病抗体的研究
引用本文:崔保安,杨明凡,李瑞芳,张素梅,王学斌,王莉. 间接ELISA检测羊伪狂犬病抗体的研究[J]. 畜牧与兽医, 2003, 35(1): 10-12
作者姓名:崔保安  杨明凡  李瑞芳  张素梅  王学斌  王莉
作者单位:河南农业大学牧医工程学院,河南,郑州,450002
摘    要:利用差速离心纯化MDBK细胞增殖伪狂犬病毒 (PRV)为抗原 ,建立间接ELISA检测伪狂犬病抗体方法。选用抗原最佳包被浓度为 1∶80 0(4μg/mL) ,酶标兔抗山羊IgG最佳稀释浓度为 1∶80 0 ,作用时间为 60min,封闭物采用 4 %明胶 ,抗原抗体最佳作用时间为 60min。根据建立的最佳反应条件检测伪狂犬病毒油乳剂灭活苗、氢氧化铝凝胶灭活苗、基因缺失油乳剂灭活苗接种山羊后的抗体消长规律。试验表明间接ELISA检测PRV抗体具有快速、敏感、特异等特点 ,适合于大量样品的检测 ,也便于畜群免疫效果的检测和免疫程序的制定

关 键 词:伪狂犬病  间接ELISA  
文章编号:0529-5130(2003)01-0010-03

Indirect ELISA for detection of antibody to PRV inactirated vaccine
CUI Bao an,YANG Ming fan,LI Rui fang,ZHANG Su mei,WANG Xue bin,WANG Li. Indirect ELISA for detection of antibody to PRV inactirated vaccine[J]. Animal Husbandry & Veterinary Medicine, 2003, 35(1): 10-12
Authors:CUI Bao an  YANG Ming fan  LI Rui fang  ZHANG Su mei  WANG Xue bin  WANG Li
Abstract:An indirect ELISA was established for detection of antibody against PRV in goat sera, employing the antigen which was the sediment through different centrifugal speed and was used to monitor the antibody dynamic regularity of goats after being immunited with inactivated vaccine. The well of an ELISA plate were coated with 0 4 μg antigen. The working titer of conjugate was 1∶800 dilution and the working time is 60 min. 4% was chosen for blocking agent. The time for antigen and antibody inter working was chosen to be 60 min. The result showed that indirect ELISA appeared correspondence in its specificity, sensitivity and repeatability test, and relatively practical for antibody surveillance of PRV.
Keywords:pseudorabies  indirect ELISA  goat
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