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. 2018 Apr 13;9:706. doi: 10.3389/fmicb.2018.00706

Table 2.

PCR primers and probes used in this study.

Name Description Sequence (5′–3′) Product size (bp)
509CF Forward primer – dPCR S509T assay GTCCCTCTTCTCCCATGCAAT 73
509CR Reverse primer – dPCR S509T assay TGCCGAAACGGATTACTCAAG 73
S509 Probe dPCR probe S509 Calorange560-AGTATGTTTTCTCGGCCAA-BHQ1 NA
T509 Probe dPCR probe T509 FAM-AGTATGTTTACTCGGCCAA-BHQ1 NA
136AF Forward primer – dPCR Y136F assay ATGCCGAAGAAATTTATACG 150
136AR Reverse primer – dPCR Y136 assay GAACTGTGCAAATATCAGAG 150
Y136 Probe dPCR probe Y136 FAM-AGGACAGTCAAACACTACA-BHQ1 NA
F136 Probe dPCR probe F136 Calorange560-AGGACAGTCATACACTACA-BHQ1 NA
Bgh51_1F Cyp51 gene sequencing primer TAGACTTCCATTTTCCGTCCT 736
Bgh51_1R Cyp51 gene sequencing primer GGGTGTGTGAAGCAGTGTATATCGT 736
Bgh51_2F Cyp51 gene sequencing primer TATCGATGCAGTAATGGCTGA 700
Bgh51_2R Cyp51 gene sequencing primer AGTGTCCCAACGATGTGGAT 700
Bgh51_3F Cyp51 gene sequencing primer AGTAAAGAATCCAATGCCCGT 528
Bgh51_3R Cyp51 gene sequencing primer CATCAATTGGCAGGTAGTGA 528
BghCYP509F Amplicon sequencing forward primer CCACCATGGTTCGCAGTTTC 280
BghCYP509R Amplicon sequencing reverse primer TGGTAGCTACGGTCCAGTCA 280

Nucleotides shown in bold are locked nucleic acids (LNA). BHQ1, Black hole quencher 1.