首页 | 本学科首页   官方微博 | 高级检索  
     检索      

长距离RT-PCR非特异性扩增的鉴定与排除
引用本文:唐青海,乔宪凤,何维明,郑新民,华文君,刘西梅,陈果亮,马秋明.长距离RT-PCR非特异性扩增的鉴定与排除[J].安徽农业科学,2007,35(15):4448-4450.
作者姓名:唐青海  乔宪凤  何维明  郑新民  华文君  刘西梅  陈果亮  马秋明
作者单位:西北农林科技大学动物科技学院,陕西杨凌,712100;湖北省畜牧兽医研究所,湖北武汉,430064;扬州大学兽医学院农业部畜禽传染病重点实验室,江苏扬州,225009
基金项目:湖北省自然科学基金项目(2005ABA195)
摘    要:根据已经测定的乙脑病毒WHe株全基因组序列(GenBank EF107527),设计1对引物扩增基因组全长cDNA和2对特异性的鉴定引物。经RT-PCR技术扩增后,得到约9 kb的产物,经过反复实验,鉴定为外源性污染核酸扩增产物,并加以有效的排除,初步的研究表明该产物可能是由外源性污染核酸自身反向部分互补扩增所致。

关 键 词:RT-PCR  乙脑病毒  非特异性扩增
文章编号:0517-6611(2007)15-04448-03
修稿时间:2006-12-18

Identification of Non-specific Amplification with Long RT-PCR
TANG Qing-hai,et al.Identification of Non-specific Amplification with Long RT-PCR[J].Journal of Anhui Agricultural Sciences,2007,35(15):4448-4450.
Authors:TANG Qing-hai  
Abstract:Two primers used to amplify the full length of Japanese encephalitis virus(JEV) WHe strain and another two pairs of primers used for identification were designed according to the complete genome of JEV-WHe strain(GenBank number,EF107527).A 9 kb cDNA fragment was produced with the long RT-PCR,and it was identified as a non-specific amplification.The research showed that this products was amplified from unknown DNA or RNA templates.
Keywords:RT-PCR  Japanese encephalitis virus  Non-specific amplification
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号