清脆的
核酸
放大器
核酸检测
多路复用
计算生物学
聚合酶链反应
PCR的应用
多重位移放大
多重聚合酶链反应
生物
生物信息学
生物化学
DNA提取
基因
作者
Siwenjie Qian,Yanju Chen,Xin Xu,Chengbin Peng,Xiaofu Wang,Hui Wu,Yang Liu,Xiao‐Ping Zhong,Junfeng Xu,Jian Wu
标识
DOI:10.1016/j.ab.2022.114593
摘要
Amplification technologies such as polymerase chain reaction (PCR) play an important role in nucleic acid detection. However, they require bulky and sophisticated thermal cycling instrument, as well as are prone to get false-positive results due to amplicon contamination. Currently, CRISPR/Cas system has become an increasingly popular diagnostic tool for nucleic acid with the discovery of its trans-cleavage activity which can degrade single-stranded DNA or RNA at a very high turnover rate. This inherent signal amplification capability allows CRISPR/Cas system to detect unamplified nucleic acids. Here, we reviewed the recent advances of CRISPR-based amplification-free methods for nucleic acid detection. With the assistance of various signal enhancement strategies, the detection sensitivity could be comparable to that of amplification-based methods. We then presented the pros and cons of these methods. And the subsistent challenges including sample preparation, off-target effect, sequences limit, quantitative and multiplex detection were further discussed in this review. It is probable for CRISPR-powered detection methods to pave the road for rapid, cheap, highly sensitive and specific on-site detection without amplification.
科研通智能强力驱动
Strongly Powered by AbleSci AI