Author: Gun-Soo Park; Keunbon Ku; Seung-Hwa Beak; Seong Jun Kim; Seung Il Kim; Bum-Tae Kim; Jin-Soo Maeng
Title: Development of Reverse Transcription Loop-mediated Isothermal Amplification (RT-LAMP) Assays Targeting SARS-CoV-2 Document date: 2020_3_12
ID: 1qn5y4gc_26
Snippet: The Limit of Detection (LoD) of optimized RT-LAMP assays were assessed through 5 to 1000 RNA copies/reaction in triplicate. Among four primer sets subjected to reaction optimization, "S_1-2-2" and "N_21" sets showed relatively poor sensitivity. For "Nsp3_1-61" and "Nsp3_2-24" primer sets, we additionally evaluated LoD with 2-fold SuperScript IV Reverse Transcriptase (20U/reaction). LoD and Tt_av were improved by increasing reverse transcriptase a.....
Document: The Limit of Detection (LoD) of optimized RT-LAMP assays were assessed through 5 to 1000 RNA copies/reaction in triplicate. Among four primer sets subjected to reaction optimization, "S_1-2-2" and "N_21" sets showed relatively poor sensitivity. For "Nsp3_1-61" and "Nsp3_2-24" primer sets, we additionally evaluated LoD with 2-fold SuperScript IV Reverse Transcriptase (20U/reaction). LoD and Tt_av were improved by increasing reverse transcriptase amount. (Table 2, Supplementary Figure 2) As a result, both "Nsp3_1-61" and "Nsp3_2-24" RT-LAMP assays could detect as low RNA concentration as 100 copies per reaction.
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