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PRRSV JL/07/SW毒株GP5重组蛋白间接ELISA检测方法的建立
引用本文:高恩鹏,丁壮,高原,孟轲音,宣华,王贵平.PRRSV JL/07/SW毒株GP5重组蛋白间接ELISA检测方法的建立[J].吉林工程技术师范学院学报,2009,25(4):72-74.
作者姓名:高恩鹏  丁壮  高原  孟轲音  宣华  王贵平
作者单位:1. 内蒙古民族大学,动物科技学院,内蒙古,通辽,028000
2. 吉林大学,畜牧兽医学院,吉林,长春,130062
3. 军事医学科学院,军事兽医研究所,吉林,长春,130062
4. 广东省农科院兽医研究所,广东,广州,510000
摘    要:本研究将以纯化的重组GP5蛋白作为包被抗原,建立了诊断PRRS的间接ELISA方法。实验确定了最佳抗原包被浓度为2.30μ/mL,PRRSV阳性血清稀释度为1:100。用间接ELISA方法检测猪瘟、猪细小病毒、猪戊肝病毒阳性血清无交叉反应,证明有很好的特异性。

关 键 词:重组质粒  重组GP5蛋白  间接ELISA

Establishment of GP5-ELISA Diagnosis Method for JL/07/SW Strain of Reproductive and Respiratory Syndrome Virus
GAO En-peng,DING Zhuang,GAO Yuan,MENG Ke-yin,XUAN Hua,WANG Gui-ping.Establishment of GP5-ELISA Diagnosis Method for JL/07/SW Strain of Reproductive and Respiratory Syndrome Virus[J].Journal of Jilin Teachers Institute of Engineering and Technology(Natural Sciences Edition),2009,25(4):72-74.
Authors:GAO En-peng  DING Zhuang  GAO Yuan  MENG Ke-yin  XUAN Hua  WANG Gui-ping
Institution:GAO En - peng, DING Zhuang, GAO Yuan , MENG Ke - yin, XUAN Hua, WANG Gui - ping ( 1. College of Animal Science and Technology, Inner Mongolia University for Nationalities, TongLiao 028000, China ; 2. College of Animal Science and Veterinary Medicine, JiILin University, Changchun Jilin 130062,China; 3. Veterinary Institute, Academy of Military Medical Science, Changchun Jilin 130062, China; 4. Cuangdong Veterinary Research Institute, Guangzhou Gnangdong 510000, China )
Abstract:Using recombined fusion GP5 protein as coating antigen set up a method of indirect enzyme - linked immtmosorbent assay (ELISA) to diagnose PRRSV. The experiment made sure of the optimal primordial covering concentration was 2.30 μg/mL. The optimal dilution of serum examinod was 1: 100. To check out among PPI(poreine parvovims infection) ; CSF(Classical swine fever )and HEV(hybrid electric vehicle) positive serum, which weren't have no cross reaction by indirect ELISA method, it improved that this method had strong specificity.
Keywords:recombinant plasmid  recombinant GP5 protein  Indirect ELISA
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