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鸡贫血病毒DNA的PCR扩增及其分子克隆 被引量:7

Amplification and Cloning of the Genomic DNA of Chicken Anemia Virus
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摘要 用PCR方法扩增了国内分离的鸡贫血病毒(CAV)SJ1株的含VP2、VP3以及部分VP1的1500bpDNA片段。经限制性内切酶酶切分析,该片段与Cux-1株的酶谱相似。同时,以pUC119质粒载体克隆了这一DNA片段。 The genomic DNA of chicken anemia virus (CAV) SJ1 strain, which was isolated from Shandong province in China, was amplified by PCR with the primers flanking a 1 500 bp DNA fragment containing the VP2, VP3 and part of VP1 genes corresponding to the nucleotide sequence of Cux 1. Endonuclease analysis of the PCR amplified DNA with the enzymes AccⅠ, BglⅡ, PvuⅡ, PstⅠ and SacⅠ showed that the restriction fragment of SJ1 strain was similar to that deduced from the nucleotide sequence from Cux 1 strain. In addition, the DNA fragment was cloned into the plasmid vector of pUC119.
出处 《中国兽医学报》 CAS CSCD 北大核心 1997年第5期417-419,共3页 Chinese Journal of Veterinary Science
基金 "九五"农业部畜牧业重点科研计划资助
关键词 鸡贫血病毒 聚合酶链反应 基因克隆 chicken anemia virus PCR gene cloning
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参考文献2

  • 1周方红,中国畜禽传染病,1996年,5卷,21页
  • 2崔现兰,中国畜禽传染病,1992年,6卷,3页

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