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

菌落PCR产物直接测序方法的建立及在水稻基因测序中的应用
引用本文:毛伟华.菌落PCR产物直接测序方法的建立及在水稻基因测序中的应用[J].中国水稻科学,2005,19(5):463-466.
作者姓名:毛伟华
作者单位:浙江大学分析测试中心,浙江,杭州,310029
基金项目:浙江省分析测试基金资助项目(04185).
摘    要: 建立了以菌落PCR 产物作为DNA 测序模板进行快速测序的技术方法。研究结果表明,采用菌落PCR技术,以载体插入位点两端序列互补的通用引物(如M13正反向引物)为引物,在控制菌落PCR反应条件的情况下,不仅可用于筛选和鉴定阳性克隆,而且菌落PCR 产物还可作为DNA 测序模板,结果准确可靠。与常规质粒测序方法比较,该法快速、简便,但对具有PolyT、PolyA过多的序列进行测序时,该法测序效率较低。

关 键 词:菌落PCR  质粒  测序  实验技术  水稻
文章编号:1001-7216(2005)05-0463-04
收稿时间:2005-03-15
修稿时间:2005-03-152005-05-07

Establishment of Direct Sequencing Method with Colony PCR Products and Its Application in Rice Gene Sequencing
MAO Wei-hua.Establishment of Direct Sequencing Method with Colony PCR Products and Its Application in Rice Gene Sequencing[J].Chinese Journal of Rice Science,2005,19(5):463-466.
Authors:MAO Wei-hua
Abstract:A method for direct sequencing using colony PCR products was established. Under controlled conditions, colony PCR could be used to screen and identify positive clone, and its products could be used as sequencing templates directly. The sequencing result was reliable. Compared with conventional plasmid DNA sequencing method, colony PCR products sequencing method was faster and simpler. However, when the products were used to sequence the DNA with long PolyT and PolyA, the sequencing efficiency was low.
Keywords:colony PCR  piasmid  sequencing  methodology  rice
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《中国水稻科学》浏览原始摘要信息
点击此处可从《中国水稻科学》下载免费的PDF全文
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