“…The final volume of the PCR reaction was 25 μL and contained 12.5 μL of 2×Power Taq PCR MasterMix (a premix and ready to use solution, including 0.1 Units/μl Taq DNA Polymerase, 500 μm dNTP Mixture each (dATP, dCTP, dGTP, dTTP), 20 mM Tris-HCl pH 8.3, 100MmKCl, 3 mMMgCl 2 , stabilizer and enhancer), 1 μL of each primer (10 μM), 1 μL genomic DNA extract and 9.5 μL deionised water. The PCR thermal cycles for the amplification of the gene regions were as described in Su et al (2015). PCR products were purified using minicolumns, purification resin and buffer according to the manufacturer's protocols (Amershamproduct code: 27-9602-01).…”