HIGHLIGHTS
SUMMARY
Genomic analyses by quantitative realtime polymerase_chain_reaction (RT-qPCR) for the detection of 3 viral genes were performed in duplicate for each collected sample, before and after the in_vitro-assays. For each infected face mask, the authors obtained several samples (in duplicate): 1) a control sample without ozone treatment for RT-qPCR assessment, 2) a sample post-ozone treatment for RT-qPCR, and 3) a sample post-ozone treatment for in_vitro assays. Mask samples were selected as appropriate for in_vitro contamination experiments when showing median Ct values (24>Ct>30) assessed by RT-qPCR (positive . . .
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