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猪CD86 mRNA定量检测方法的建立
引用本文:周双海,杨汉春,郭鑫,陈艳红,查振林.猪CD86 mRNA定量检测方法的建立[J].北京农学院学报,2006,21(2):33-35.
作者姓名:周双海  杨汉春  郭鑫  陈艳红  查振林
作者单位:中国农业大学,动物医学院,北京,100094;北京农学院,动物科学技术系,北京,102206;中国农业大学,动物医学院,北京,100094
基金项目:教育部跨世纪优秀人才培养计划
摘    要:用RT-PCR技术从猪肺泡巨噬细胞中扩增和克隆了猪CD86基因部分片段,经测序鉴定后,用反向PCR技术构建了CD86的缺失竞争cDNA分子。通过竞争PCR方法,建立了CD86标准竞争曲线,并得到其直线回归方程。本方法操作简单,特异性和敏感性高,可用于猪CD86 mRNA水平的定量检测。

关 键 词:  CD86  竞争PCR
文章编号:1002-3186(2006)02-0033-03
收稿时间:2005-10-10
修稿时间:2005-12-30

Development of Quantitative Detection of Porcine CD86 mRNA
ZHOU Shuang-hai,YANG Han-chun,GUO Xin,CHEN Yan-hong,ZHA Zhen-lin.Development of Quantitative Detection of Porcine CD86 mRNA[J].Journal of Beijing Agricultural College,2006,21(2):33-35.
Authors:ZHOU Shuang-hai  YANG Han-chun  GUO Xin  CHEN Yan-hong  ZHA Zhen-lin
Institution:1. College of Veterinary Medicine, China Agricultural University, Beijing 100094,China; 2. Department of Animal Science and Veterinary Medicine, Beijing Agricultural College, Beijing 102206, China
Abstract:Porcine CD86 was amplified by RT-PCR from porcine alveolar macrophages and cloned.Following sequencing,competitive depletion clones for the cDNA molecules was generated by reverse PCR.Then,the linear regression equation was obtained after construction of the standard competitive curves by quantitative competitive PCR assay.This study provided a simple,high specific and sensitive method for defecting porcine CD86 mRNA level.
Keywords:porcine  CD86  competitive PCR
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