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Updated: Oct 8, 2025

Field-Deployable Candidatus Liberibacter asiaticus Detection Using Recombinase Polymerase Amplification Combined with CRISPR-Cas12a
Published on: December 23, 2022
CRISPR/Cas12a collateral cleavage activity for an ultrasensitive assay of RNase H
Hansol Kim1, Seoyoung Lee1, Jinhwan Lee1
1Department of Chemical and Biomolecular Engineering (BK 21+ program), Korea Advanced Institute of Science and Technology (KAIST), Daehak-ro 291, Yuseong-gu, Daejeon 34141, Republic of Korea. hgpark@kaist.ac.kr.
Abstract:
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.
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