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猪伪狂犬病PCR诊断方法的建立
引用本文:陈钟鸣,张定东.猪伪狂犬病PCR诊断方法的建立[J].动物医学进展,2006,27(2):83-85.
作者姓名:陈钟鸣  张定东
作者单位:金陵科技学院动物科学系,江苏南京,210038;金陵科技学院动物科学系,江苏南京,210038
摘    要:根据伪狂犬病病毒(PRV)gB基因的序列,设计并合成了一对引物,以闽A株细胞培养毒为模板,筛选最佳反应条件,建立了检测PRV的PCR方法,应用本方法对分离的病毒进行基因扩增,获得了217bp的特异性DNA片段,证明了对分离病毒检测的特异性和敏感性,为伪狂犬病的快速诊断提供了条件。

关 键 词:多聚酶链式反应  伪狂犬病病毒
文章编号:1007-5038(2006)02-0083-03
收稿时间:2005-10-17
修稿时间:2005年10月17

The Establishment of PCR Diagnositic Technique of Porcine Pseudorabies
CHEN Zhong-ming,ZHANG Ding-dong.The Establishment of PCR Diagnositic Technique of Porcine Pseudorabies[J].Progress In Veterinary Medicine,2006,27(2):83-85.
Authors:CHEN Zhong-ming  ZHANG Ding-dong
Institution:Departraent of Animal Science, Jinling Institute of Technology, Nanj ing, Jiangsu, 210038, China
Abstract:One pair of pri mers that amplifiedthe gBgene of Pseudorabies virus(PRV) was designed and syn-thesized,PCRtechnique detectingthe DNAof PRV was established after selectingthe best reaction condi-tions.This technique was applied to specifically amplify the 217 bp DNAfragment of the PRV.The re-sults showed that the establishment of PRV PCRtechnique provided a more sensitive,specific and reliablemethod for pseudorabies diagnosis.
Keywords:PCR  Pseudorabies virus
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