清脆的
反式激活crRNA
环介导等温扩增
计算生物学
核酸酶
生物
核酸
检测点注意事项
DNA
基因组编辑
遗传学
免疫学
基因
作者
Xin Li,Zhisheng Dang,Wenqiang Tang,Haoji Zhang,Jian‐Wei Shao,Rui Jiang,Xu Zhang,Fuqiang Huang
出处
期刊:Biosensors
[MDPI AG]
日期:2024-03-14
卷期号:14 (3): 145-145
被引量:2
摘要
The rapid and accurate identification of parasites is crucial for prompt therapeutic intervention in parasitosis and effective epidemiological surveillance. For accurate and effective clinical diagnosis, it is imperative to develop a nucleic-acid-based diagnostic tool that combines the sensitivity and specificity of nucleic acid amplification tests (NAATs) with the speed, cost-effectiveness, and convenience of isothermal amplification methods. A new nucleic acid detection method, utilizing the clustered regularly interspaced short palindromic repeats (CRISPR)-associated (Cas) nuclease, holds promise in point-of-care testing (POCT). CRISPR/Cas12a is presently employed for the detection of
科研通智能强力驱动
Strongly Powered by AbleSci AI