重组酶聚合酶扩增
PCR的应用
聚合酶
计算机科学
计算生物学
聚合酶链反应
生物
DNA
数字聚合酶链反应
遗传学
基因
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI