The coronavirus disease 2019 (COVID-19) pandemic now has >2,000,000 confirmed cases worldwide. COVID-19 is currently diagnosed using quantitative RT-PCR methods, but the capacity of quantitative RT-PCR methods is limited by their requirement of high-level facilities and instruments. We developed and evaluated reverse transcription loop-mediated isothermal amplification (RT-LAMP) assays to detect genomic RNA of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative virus of COVID-19. RT-LAMP assays reported in this study can detect as low as 100 copies of SARS-CoV-2 RNA. Cross-reactivity of RT-LAMP assays to other human coronaviruses was not observed. A colorimetric detection method was adapted for this RT-LAMP assay to enable higher throughput.
Development of Reverse Transcription Loop-Mediated Isothermal Amplification Assays Targeting Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2).
针对严重急性呼吸综合征冠状病毒 2 (SARS-CoV-2) 的逆转录环介导等温扩增检测方法的开发
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作者:Park Gun-Soo, Ku Keunbon, Baek Seung-Hwa, Kim Seong-Jun, Kim Seung Il, Kim Bum-Tae, Maeng Jin-Soo
| 期刊: | Journal of Molecular Diagnostics | 影响因子: | 3.400 |
| 时间: | 2020 | 起止号: | 2020 Jun;22(6):729-735 |
| doi: | 10.1016/j.jmoldx.2020.03.006 | 疾病类型: | 新冠 |
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