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. 2016 Jan 31;32(1):81–87. doi: 10.5487/TR.2016.32.1.081

Table 4.

The oligonucleotide primer pairs used for SYBR green real-time PCR amplifications

No Primer pairs Gene Primer sequence (5′-3′) Annealing temperature
1 Tub1-F
Tub1-R
tub1 GTC CGG TGC TGG TAA CAA CT
GGA GGT GGA GTT TCC AAT GA
65
2 Ver1
Ver2
aflM GCC GCA CGC GGA GAA AGT GGT
GGG GAT ATA CTC CCG CGA CAC AGC C
65
3 aflR 660
aflR 1249
aflR CGC GCT CCC AGT CCC CTT CAT T
CTT GTT CCC CGA GAT GAC CA
59
4 nor1
nor2
aflD ACC GCT ACG CCG GCA CTC TCG GCA C
GTT GGC CGC CAG CTT CGA CAC TCC G
65

The oligonucleotide primer pairs were used to target the specific fungal genes: Tub1-F and Tub1-R for tub1; Ver1 and Ver2 for aflM (versicolorin A); aflR 660 and aflR 1249 for aflR; nor1 and nor2 (norsolorinic acid) for aflD.