化学
反式激活crRNA
环介导等温扩增
核酸
DNA
分子生物学
计算生物学
生物化学
基因组编辑
清脆的
基因
生物
作者
Qinlong Zeng,Miaojin Zhou,Weiheng Deng,Qian Gao,Zhuo Li,Lingqian Wu,Desheng Liang
标识
DOI:10.1016/j.aca.2024.342693
摘要
CRISPR-Cas12a based one-step assays are widely used for nucleic acid detection, particularly for pathogen detection. However, the detection capability of the one-step assay is reduced because the Cas12a protein competes with the isothermal amplification enzymes for the target DNA and cleaves it. Therefore, the key to improving the sensitivity of the one-step assay is to address the imbalance between isothermal amplification and CRISPR detection. In previous study, we developed a Cas12a one-step assay using single-stranded DNA (ssDNA)-modified crRNA (mD-crRNA) and applied this method for the detection of pathogenic DNA.
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