Journal
RSC CHEMICAL BIOLOGY
Volume 2, Issue 4, Pages 1201-1205Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1cb00076d
Keywords
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Funding
- National Natural Science Foundation of China (NSFC) [21822704, 21778040, 91940304, 22037004, 91753201, 21721005, 21778041]
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A one-pot fluorescence-based assay was developed to quantitatively detect A3A activity by combining cytosine deamination and uracil excision. The fluorescent turn-on effect at 520 nm can be used to evaluate A3A activity and screen inhibitors.
We reported a one-pot fluorescence-based assay to quantitively detect A3A activity combined with cytosine deamination and uracil excision. After deamination by A3A and USER enzyme treatment, the fluorescent turn-on effect at 520 nm was observed, which can be used to evaluate the A3A activity and screen inhibitors.
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