首页> 外国专利> METHOD FOR DISCRIMINATION OF NONHUMAN ANIMAL INFECTED WITH PARAHYDROPHOBIA VIRUS AND KIT FOR SAID METHOD

METHOD FOR DISCRIMINATION OF NONHUMAN ANIMAL INFECTED WITH PARAHYDROPHOBIA VIRUS AND KIT FOR SAID METHOD

机译:鉴别副嗜血杆菌病毒和试剂盒的非人类动物鉴别方法。

摘要

PROBLEM TO BE SOLVED: To identify an animal infected with Pseudo Rabies Virus(PRV) by subjecting a morbid animal to vaccination of PRV lacking glycoprotein gI or gp63. SOLUTION: pPR28 is consumed by PVuII and a cut piece, containing E.coli replication start point and bla gene, is recirculated to produce a plasmid comprising 4.9kbPvuII/BamH17 PVR fragment containing DNA arrangement for gI thus obtaining plasmid pPR28-1. BamH17 is subjected to subcloning, consumed, labeled and arranged. DNA arrangements for glycoprotein gp63 and gI are presented on arrangement tables (arrangement number 2 and 3). An animal infected actively with PRV can be detected using this DNA. Presence of PRV can be detected by wiping nose or throat using a cotton swab for the purpose of sampling and subjecting the sample to a standard hybridization of DNA/DNA.
机译:要解决的问题:通过使病态的动物接种缺乏糖蛋白gI或gp63的PRV,来鉴定感染了伪狂犬病病毒(PRV)的动物。解决方案:pPR28被PVuII消耗,包含大肠杆菌复制起点和bla基因的切割片段被再循环以产生包含4.9kbPvuII / BamH17 PVR片段的质粒,该片段含有gI的DNA排列,从而获得了质粒pPR28-1。 BamH17进行亚克隆,消耗,标记和排列。糖蛋白gp63和gI的DNA排列在排列表中(排列编号2和3)。可以使用该DNA检测出被PRV活跃感染的动物。可以通过棉签擦拭鼻子或喉咙来检测PRV的存在,以进行采样并将样品进行标准的DNA / DNA杂交。

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