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10.4269/ajtmh.21-0150

http://scihub22266oqcxt.onion/10.4269/ajtmh.21-0150
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suck abstract from ncbi


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pmid34129521      Am+J+Trop+Med+Hyg 2021 ; 105 (2): 375-377
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  • Colorimetric Reverse Transcription-Loop-Mediated Isothermal Amplification Assay for Rapid Detection of SARS-CoV-2 #MMPMID34129521
  • Lai MY; Tang SN; Lau YL
  • Am J Trop Med Hyg 2021[Jun]; 105 (2): 375-377 PMID34129521show ga
  • Coronavirus disease 2019 (COVID-19), which is caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has been spreading rapidly all over the world. In the absence of effective treatments or a vaccine, there is an urgent need to develop a more rapid and simple detection technology of COVID-19. We describe a WarmStart colorimetric reverse transcription-loop-mediated isothermal amplification (RT-LAMP) assay for the detection of SARS-CoV-2. The detection limit for this assay was 1 copy/microL SARS-CoV-2. To test the clinical sensitivity and specificity of the assay, 37 positive and 20 negative samples were used. The WarmStart colorimetric RT-LAMP had 100% sensitivity and specificity. End products were detected by direct observation, thereby eliminating the need for post-amplification processing steps. WarmStart colorimetric RT-LAMP provides an opportunity to facilitate virus detection in resource-limited settings without a sophisticated diagnostic infrastructure.
  • |COVID-19 Nucleic Acid Testing/*methods/standards[MESH]
  • |COVID-19/*diagnosis/virology[MESH]
  • |Colorimetry/*methods/standards[MESH]
  • |Humans[MESH]
  • |Molecular Diagnostic Techniques/*methods/standards[MESH]
  • |Nasopharynx/virology[MESH]
  • |Nucleic Acid Amplification Techniques/*methods/standards[MESH]
  • |RNA, Viral/genetics[MESH]
  • |SARS-CoV-2/*genetics/isolation & purification[MESH]


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