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Base excision repair initiated rolling circle amplification-based fluorescent assay for screening uracil-DNA glycosylase activity using Endo IV-assisted cleavage of AP probes
The Analyst Pub Date : 2018-07-03 , DOI: 10.1039/c8an00716k Jingfeng Wang 1, 2, 3, 4 , Yu Wang 1, 2, 3, 4 , Su Liu 2, 3, 4, 5 , Haiwang Wang 1, 2, 3, 4 , Xue Zhang 1, 2, 3, 4 , Xiaolei Song 2, 3, 4, 5 , Jiadong Huang 1, 2, 3, 4, 6
中文翻译:
碱基切除修复启动基于滚环扩增的荧光测定,使用 Endo IV 辅助 AP 探针切割筛选尿嘧啶-DNA 糖基化酶活性
更新日期:2018-07-03
The Analyst Pub Date : 2018-07-03 , DOI: 10.1039/c8an00716k Jingfeng Wang 1, 2, 3, 4 , Yu Wang 1, 2, 3, 4 , Su Liu 2, 3, 4, 5 , Haiwang Wang 1, 2, 3, 4 , Xue Zhang 1, 2, 3, 4 , Xiaolei Song 2, 3, 4, 5 , Jiadong Huang 1, 2, 3, 4, 6
Affiliation
A simple, robust and cost effective biosensing platform for the ultrasensitive detection of UDG activity was established based on base excision repair-initiated primer generation for RCA with Endo IV-assisted signal amplification.
中文翻译:
碱基切除修复启动基于滚环扩增的荧光测定,使用 Endo IV 辅助 AP 探针切割筛选尿嘧啶-DNA 糖基化酶活性
基于碱基切除修复启动的 RCA 引物生成和 Endo IV 辅助信号放大,建立了一个简单、稳健且具有成本效益的生物传感平台,用于超灵敏检测 UDG 活性。