Suppr超能文献

长程反向PCR(LR-IPCR):扩展反向PCR的有效范围。

Long range-inverse PCR (LR-IPCR): extending the useful range of inverse PCR.

作者信息

Benkel B F, Fong Y

机构信息

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

出版信息

Genet Anal. 1996 Nov;13(5):123-7. doi: 10.1016/s1050-3862(96)00161-1.

Abstract

The inverse PCR technique (IPCR) has proven to be very useful for the amplification of uncharacterized stretches of DNA upstream or downstream of regions that have already been cloned and sequenced. In practice, however, chromosome walking using standard IPCR is often a slow, repetitive process because only small DNA fragments are effectively amplified. The development of long and accurate PCR methodology has greatly expanded the range of DNA fragment sizes that is amenable to amplification by conventional PCR. We reasoned that combining long range PCR with IPCR would also extend the useful range of the IPCR technique. In this paper we demonstrate the utility of the hybrid, long range-inverse PCR (LR-IPCR) technique by generating clones containing long stretches of DNA flanking endogenous chicken proviral elements.

摘要

反向PCR技术(IPCR)已被证明对于扩增已克隆和测序区域上游或下游未表征的DNA片段非常有用。然而在实际操作中,使用标准IPCR进行染色体步移往往是一个缓慢、重复的过程,因为只有小的DNA片段能被有效扩增。长片段且准确的PCR方法的发展极大地扩展了适合常规PCR扩增的DNA片段大小范围。我们推测将长片段PCR与IPCR相结合也会扩展IPCR技术的适用范围。在本文中,我们通过生成包含内源性鸡前病毒元件侧翼长片段DNA的克隆,证明了长片段-反向PCR(LR-IPCR)杂交技术的实用性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验