A digital PCR-based protocol to detect and quantify RNA editing events at hotspots
Summary: APOBEC3A, CRISPR programmable RNA base editors, or other enzymes can edit RNA transcripts at specific locations or hotspots. Precise quantification of these RNA-editing events is crucial to determine the activity and efficiency of these enzymes in cells. We have developed a quick method to...
Main Authors: | Sunwoo Oh, Rémi Buisson |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2022-03-01
|
Series: | STAR Protocols |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2666166722000284 |
Similar Items
-
Protocol for precision editing of endogenous Chlamydomonas reinhardtii genes with CRISPR-Cas
by: Adrian Pascal Nievergelt, et al.
Published: (2024-03-01) -
A user-friendly and streamlined protocol for CRISPR/Cas9 genome editing in budding yeast
by: Daniele Novarina, et al.
Published: (2022-06-01) -
Optimized protocols for efficient gene editing in mouse hepatocytes in vivo using CRISPR-Cas9 technology
by: Yanhao Chen, et al.
Published: (2022-03-01) -
Protocol for targeted modification of the rice genome using base editing
by: Meixia Wang, et al.
Published: (2022-12-01) -
Genome editing in Penicillium funiculosum using in vitro assembled CRISPR-Cas9 ribonucleoprotein complexes
by: Tulika Sinha, et al.
Published: (2022-09-01)