A novel fluorescence amplification strategy combining cascade primer exchange reaction with CRISPR/Cas12a system for ultrasensitive detection of RNase H activity-Reference-Cited by-同舟云学术

A novel fluorescence amplification strategy combining cascade primer exchange reaction with CRISPR/Cas12a system for ultrasensitive detection of RNase H activity

Published:2022-06 Issue: Volume:206 Page:114135
ISSN:0956-5663
Container-title:Biosensors and Bioelectronics
language:en
Short-container-title:Biosensors and Bioelectronics

Author:

Xie Zuowei,Chen Siyi,Zhang Wenxiu,Zhao Shuhui,Zhao Zixin,Wang Xingyu,Huang Yuqi,Yi Gang

Funder

Chongqing Municipal Education Commission

Publisher

Elsevier BV

Subject

Electrochemistry,Biomedical Engineering,General Medicine,Biophysics,Biotechnology

Reference40 articles.

1. Chemoenzymatic total synthesis of potent HIV RNase H inhibitor (−)-1,3,4,5-tetragalloylapiitol

2. Terminal deoxynucleotidyl transferase induced activators to unlock the trans-cleavage of CRISPR/Cpf 1 (TdT-IU- CRISPR/Cpf 1): An ultrasensitive biosensor for Dam MTase activity detection

3. CRISPR-Cas12a target binding unleashes indiscriminate single-stranded DNase activity

4. Exploring the Trans‐Cleavage Activity of CRISPR‐Cas12a (cpf1) for the Development of a Universal Electrochemical Biosensor

5. Selective inhibition of RNase H by dextran.

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