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. 2022 Mar 24;34(2):118–124. doi: 10.5021/ad.2022.34.2.118

Table 1. Primers used in the real-time qPCR assay.

Name Sequence (5’-3’) Characterization
ITS1 F TGC GTT CTT CAT CGA TGC GA Pan-fungal primer (Forward)
ITS4 R TAA GCG CAA GTC ATC AGC TTG CGT Pan-fungal primer (Reverse)
ITS1 F TAA GCG CAA GTC ATC AGC TTG CGT T Pan-Candida primer (Forward)
5.8S1R TGC GTT CTT CAT CGA TGC GA Pan-Candida primer (Reverse)
ITS1 F2 SSC CCC ATT CTT GTC TAC MTY AC Trichophyton detection (Forward)
ITS R2 AAC GCT CAG ACT GAC AGC TCT TC Trichophyton detection (Reverse)
MC F CCT AAG CGG TGG GTG GTT ACT Microsporum detection (Forward)
MC R TGA AAG AAC ATA CCG TCT GAG CG Microsporum detection (Reverse)

The primer sequences shown in this table were previously published10,11,12. ITS: internal transcribed spacer, MC F: Microsporum canis forward, MC R: M. canis reverse.