“…Amplification was carried out in 50 l of PCR mix, which included 10 l of genomic DNA, 25 l of 2x My Taq HS Red Mix (Bioline), 0.5 M of each primer, 0.2 g of bovine serum albumin (BSA), and sterile water. DNA amplification was carried out in an Applied Biosystem ProFlex PCR system using a program consisting of 5 minutes of denaturation at 94°C, 35 cycles of 94°C for 30 seconds, 55 °C for 30 seconds, 72 °C for 60 seconds, and a final extension at 72 °C for 7 minutes, as in a previous study [32]. The ITS DNA amplicon was observed by electrophoresis on agarose gel using 1x TBE buffer at 110 volts for approximately 45 minutes.…”