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. 2020 Aug 13;7:521. doi: 10.3389/fmed.2020.00521

Table 1.

Specifications and PCR conditions of the four commercial kits used for SARS-CoV-2 RNA detection.

Kit name, manufacturer PCR equipment Target genes/No. tubes Internal control Volume of RNA eluates per test (μL) No. amplification cycles Running time of PCR Cutoff Ct
Allplex 2019-nCoV, Seegene CFX96 E, RdRp, N/one Bacteriophage MS2, spiked into sample 8 45 110 min <40
PowerChek 2019-nCoV Real-time PCR, Kogene Biotech CFX96, ABI7500, Gentier96 E, RdRp/two Recombinant DNA plasmid spiked into PCR mixture 5 40 120 min ≤35
Real-Q 2019-nCoV Detection, BioSewoom CFX96, ABI7500 E, RdRp/one Human RNase P, intrinsic 5 40 110 min Target gene: <38, Internal control: ≤35
StandardM nCoV Real-Time Detection, SD Biosensor CFX96, ABI7500, LC480 E, RdRp/one Pseudovirus particle, spiking of 5 μL into sample or 0.5 μL into PCR mixture 10 45, including 5 pre-amplifications 90 min Target gene: ≤36*, Internal control: ≤32*

SARS-CoV-2, severe acute respiratory syndrome coronavirus 2; Ct, cycle threshold.

*

Pre-amplification was not counted for Ct.