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10.1016/j.cca.2020.04.023

http://scihub22266oqcxt.onion/10.1016/j.cca.2020.04.023
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32335089!7179514!32335089
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suck abstract from ncbi


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pmid32335089      Clin+Chim+Acta 2020 ; 507 (ä): 139-142
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  • Highly sensitive detection of SARS-CoV-2 RNA by multiplex rRT-PCR for molecular diagnosis of COVID-19 by clinical laboratories #MMPMID32335089
  • Ishige T; Murata S; Taniguchi T; Miyabe A; Kitamura K; Kawasaki K; Nishimura M; Igari H; Matsushita K
  • Clin Chim Acta 2020[Aug]; 507 (ä): 139-142 PMID32335089show ga
  • BACKGROUND: The detection of SARS-CoV-2 RNA by real-time reverse transcription-polymerase chain reaction (rRT-PCR) is used to confirm the clinical diagnosis of COVID-19 by molecular diagnostic laboratories. We developed a multiplex rRT-PCR methodology for the detection of SARS-CoV-2 RNA. METHODS: Three genes were used for multiplex rRT-PCR: the Sarbecovirus specific E gene, the SARS-CoV-2 specific N gene, and the human ABL1 gene as an internal control. RESULTS: Good correlation of C(q) values was observed between the simplex and multiplex rRT-PCR methodologies. Low copies (<25 copies/reaction) of SARS-CoV-2 RNA were detected by the novel multiplex rRT-PCR method. CONCLUSION: The proposed multiplex rRT-PCR methodology will enable highly sensitive detection of SARS-CoV-2 RNA, reducing reagent use and cost, and time required by clinical laboratory technicians.
  • |*Multiplex Polymerase Chain Reaction[MESH]
  • |*Reverse Transcriptase Polymerase Chain Reaction/methods/standards[MESH]
  • |Betacoronavirus/*genetics/isolation & purification[MESH]
  • |COVID-19[MESH]
  • |COVID-19 Testing[MESH]
  • |COVID-19 Vaccines[MESH]
  • |Clinical Laboratory Techniques/*methods/standards[MESH]
  • |Coronavirus Infections/*diagnosis/*genetics[MESH]
  • |Humans[MESH]
  • |Pandemics[MESH]
  • |Pneumonia, Viral/*diagnosis/genetics[MESH]
  • |RNA, Viral/*genetics/isolation & purification[MESH]
  • |Real-Time Polymerase Chain Reaction/methods/standards[MESH]
  • |Reproducibility of Results[MESH]
  • |SARS-CoV-2[MESH]


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