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10.1038/s41467-021-21121-7

http://scihub22266oqcxt.onion/10.1038/s41467-021-21121-7
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33547323!7864991!33547323
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suck abstract from ncbi


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pmid33547323      Nat+Commun 2021 ; 12 (1): 802
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  • Rapid electrochemical detection of coronavirus SARS-CoV-2 #MMPMID33547323
  • Chaibun T; Puenpa J; Ngamdee T; Boonapatcharoen N; Athamanolap P; O'Mullane AP; Vongpunsawad S; Poovorawan Y; Lee SY; Lertanantawong B
  • Nat Commun 2021[Feb]; 12 (1): 802 PMID33547323show ga
  • Coronavirus disease 2019 (COVID-19) is a highly contagious disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Diagnosis of COVID-19 depends on quantitative reverse transcription PCR (qRT-PCR), which is time-consuming and requires expensive instrumentation. Here, we report an ultrasensitive electrochemical biosensor based on isothermal rolling circle amplification (RCA) for rapid detection of SARS-CoV-2. The assay involves the hybridization of the RCA amplicons with probes that were functionalized with redox active labels that are detectable by an electrochemical biosensor. The one-step sandwich hybridization assay could detect as low as 1 copy/muL of N and S genes, in less than 2 h. Sensor evaluation with 106 clinical samples, including 41 SARS-CoV-2 positive and 9 samples positive for other respiratory viruses, gave a 100% concordance result with qRT-PCR, with complete correlation between the biosensor current signals and quantitation cycle (Cq) values. In summary, this biosensor could be used as an on-site, real-time diagnostic test for COVID-19.
  • |Biosensing Techniques/*methods[MESH]
  • |COVID-19/*diagnosis/virology[MESH]
  • |Electrochemical Techniques/*methods[MESH]
  • |Humans[MESH]
  • |Nucleic Acid Amplification Techniques/methods[MESH]
  • |RNA, Viral/genetics[MESH]
  • |SARS-CoV-2/genetics/*isolation & purification/physiology[MESH]


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