“…The amplification reactions were carried out with the following protocol: 50 μl reaction volume containing 2 µl of DNA template, 2 µl of each forward and reverse primers, 25 µl of 2 × Bench Top TM Taq Master Mix (mixture of Taq DNA Polymerase (recombinant): 0.05 units/µl, MgCl 2 : 4 mM and dNTPs (dATP, dCTP, dGTP, dTTP): 0.4 mM) and 19 µl of double-distilled water (ddH 2 O) (sterilised water) using the thermal cycle programme in
Norphanphoun et al (2017). Purification and sequencing of
PCR products with the same primers mentioned above were carried out at Life Biotechnology Co., Shanghai, China.…”