Suppr超能文献

一种基于聚合酶链式反应(PCR)的快速检测鸡内源性病毒元件ev3的方法。

A rapid PCR-based test for the endogenous viral element ev3 of chickens.

作者信息

Benkel B F, Perreault J, Gagnon C, Conklin K

机构信息

Agriculture and AgriFood Canada, Centre for Food and Animal Research, Ottawa, Ontario.

出版信息

Anim Genet. 1995 Jun;26(3):189-91. doi: 10.1111/j.1365-2052.1995.tb03161.x.

Abstract

A short fragment of chicken genomic DNA encompassing the insertion site of the endogenous avian leucosis viral element ev3 was isolated using the inverse polymerase chain reaction (inverse PCR) technique. The nucleotide sequence of the unoccupied site was used to design PCR primers that can be used to unambiguously determine the genetic status of any chicken, with respect to ev3. Screening of a small number of individuals from exotic breeds of chickens suggested that the frequency of ev3 is highly variable. The ev3 integration site shows a high degree of sequence homology with the macrophage-specific tyrosine kinase gene, bmk, in mice.

摘要

利用反向聚合酶链反应(Inverse PCR)技术分离出一段包含内源性禽白血病病毒元件ev3插入位点的鸡基因组DNA短片段。利用未被占据位点的核苷酸序列设计PCR引物,可用于明确确定任何鸡相对于ev3的遗传状态。对少数外来品种鸡个体的筛选表明,ev3的频率高度可变。ev3整合位点与小鼠巨噬细胞特异性酪氨酸激酶基因bmk具有高度的序列同源性。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验