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Rapid and Specific Detection of Active SARS-CoV-2 With CRISPR/Cas12a

Front Microbiol. 2022-01; 
Xinyi Liu , Yanhua Li , Xin Wang , Yifan Song , Lina Wu , Benyuan Yu , Xiaodong Ma , Peixiang Ma, Ming Liu , Xingxu Huang , Xinjie Wang
Products/Services Used Details Operation
Gene Synthesis The primers used to amplify SARS-CoV-2 (GenBank: MN908947) subgenomic sequences were designed and synthesized by GenScript (Nanjing, China). Get A Quote
Custom DNA/RNA Oligos Get A Quote

摘要

Rapid and sensitive nucleic acid detection of SARS-CoV-2 has contributed to the clinical diagnosis and control of COVID-19. Although detection of virus genomic RNA (gRNA) has been commonly used in clinical diagnosis, SARS-CoV-2 gRNA detection could not discriminate between active infectious virus with remnant viral RNA. In contrast to genomic RNA, subgenomic RNAs (sgRNAs) are only produced when the virus is actively replicating and transcription, detection of sgRNA could be an indication to evaluate infectivity. CRISPR/Cas-based nucleic acid detection methods have been considered potential diagnostic tools due to their intrinsic sensitivity, specificity and simplicity. In this study, to specifically detect acti... More

關鍵詞

COVID-19; CRISPR-based detection; CRISPR/Cas12a; SARS-CoV-2; virus subgenome.
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