CRISPR/Cas12a collateral cleavage activity for an ultrasensitive assay of RNase H

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We herein describe an ultrasensitive RNase H assay by utilizing CRISPR/Cas12a collateral cleavage activity. Based on this unique design principle, the RNase H activity was successfully determined down to 0.00024 U mL(-1), which is quite superior to those of alternative approaches.
Publisher
ROYAL SOC CHEMISTRY
Issue Date
2022-02
Language
English
Article Type
Article
Citation

CHEMICAL COMMUNICATIONS, v.58, no.16, pp.2654 - 2657

ISSN
1359-7345
DOI
10.1039/d1cc06026k
URI
http://hdl.handle.net/10203/292402
Appears in Collection
CBE-Journal Papers(저널논문)
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