重组酶聚合酶扩增
环介导等温扩增
PCR的应用
多重位移放大
聚合酶
计算机科学
纳米技术
计算生物学
重组酶
聚合酶链反应
生物
DNA
数字聚合酶链反应
材料科学
遗传学
重组
基因
DNA提取
作者
Iván Lobato,Ciara K. O’Sullivan
标识
DOI:10.1016/j.trac.2017.10.015
摘要
Recombinase polymerase amplification (RPA) is a highly sensitive and selective isothermal amplification technique, operating at 37-42°C, with minimal sample preparation and capable of amplifying as low as 1-10 DNA target copies in less than 20 min. It has been used to amplify diverse targets, including RNA, miRNA, ssDNA and dsDNA from a wide variety of organisms and samples. An ever increasing number of publications detailing the use of RPA are appearing and amplification has been carried out in solution phase, solid phase as well as in a bridge amplification format. Furthermore, RPA has been successfully integrated with different detection strategies, from end-point lateral flow strips to real-time fluorescent detection amongst others. This review focuses on the different methodologies and advances related to RPA technology, as well as highlighting some of the advantages and drawbacks of the technique.
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