Randomized PAM depeletion of NmeCas9. Randomized PAM depeletion of NmeCas9
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https://www.ncbi.nlm.nih.gov/bioproject/PRJNA423256
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We report the PAMs of NmeCas9 using a cell-free TXTL-based cleavage assay. By adding randomized PAM library and NmeCas9-gRNA in vitro, functional PAM sequences were cleaved, while non-functional PAMs remained. By amplifying the non-cleaved DNA, we use next-generation sequencing to analyze the depletion of functional PAMs of NmeCas9. Overall design: Pam determination assay for NmeCas9
本研究基于无细胞转录翻译偶联(Transcription-translation coupled, TXTL)裂解检测实验,报道了NmeCas9的原间隔序列邻近基序(Protospacer Adjacent Motif, PAM)。通过体外添加随机化PAM文库与NmeCas9-向导RNA(guide RNA, gRNA)复合物,具备功能的PAM序列会被切割,而非功能PAM则得以保留。通过扩增未被切割的DNA,我们利用下一代测序(Next-Generation Sequencing, NGS)分析NmeCas9功能PAM的耗竭情况。实验整体设计:NmeCas9的PAM鉴定检测实验
创建时间:
2017-12-20



