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应用逆转录套式PCR检测猪流行性腹泻病毒
引用本文:王金良,谢金文,唐娜,祖立闯,李娇,汪洋,沈志强.应用逆转录套式PCR检测猪流行性腹泻病毒[J].中国畜牧兽医,2012,39(9):86-88.
作者姓名:王金良  谢金文  唐娜  祖立闯  李娇  汪洋  沈志强
作者单位:1. 山东省滨州畜牧兽医研究院,山东滨州 256600;
2. 山东绿都生物科技有限公司,山东滨州 256600
基金项目:山东省自然科学基金资助项目
摘    要:根据已发表的猪流行性腹泻病毒(PEDV)N基因核苷酸序列,设计合成2对引物,其中外引物扩增片段长度为297 bp,内引物扩增片段长度为212 bp,在优化RT-PCR反应条件的基础上,建立了检测PEDV的套式RT-PCR检测方法,该方法较普通RT-PCR更加灵敏、可靠,能有效降低假阳性和污染,可用于PEDV的快速诊断和流行病学调查。

关 键 词:猪流行性腹泻病毒  N基因  套式RT-PCR  检测  
收稿时间:2012-03-21

Detection of Porcine Epidemic Diarrhea Virus by RT-nested PCR
WANG Jin-liang , XIE Jin-wen , TANG Na , ZU Li-chuang , LI Jiao , WANG Yang , SHEN Zhi-qiang.Detection of Porcine Epidemic Diarrhea Virus by RT-nested PCR[J].China Animal Husbandry & Veterinary Medicine,2012,39(9):86-88.
Authors:WANG Jin-liang  XIE Jin-wen  TANG Na  ZU Li-chuang  LI Jiao  WANG Yang  SHEN Zhi-qiang
Institution:1. Shandong Binzhou Academy of Animal Science and Veterinary Medicine, Binzhou 256600, China;
2. Shandong Lvdu Biological Technology Co., Ltd., Binzhou 256600, China
Abstract:Based on the published nucleotide sequence of porcine epidemic diarrhea virus N gene,two pairs of primers were designed and synthesized,which outer primers amplified fragment length was 297 bp,and inner primers amplified fragment length was 212 bp.RT-nested PCR methods had been established through optimization of the RT-PCR reaction conditions,this method was more sensitive and reliable than ordinary RT-PCR,and could effectively reduce the false positive and pollution.It could be used for rapid diagnosis and epidemiological investigation of the PEDV.
Keywords:PEDV  N gene  RT-nested PCR  detection
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