“…For the extraction of DNA, hexadecyltrimethylammonium bromide CTAB protocol was used as described by [21] and then quantified [17]. A total of 9 polymorphic and informative microsatellite primers developed for Parkia panurensis (Parpan 3, Parpan 4, Parpan 5, Parpan 9, Parpan11, Parpan13, Parpan14, Parpan15, and Parpan 21) (Table 1) were validated in heterologous amplification [22] and were used in the study. These microsatellite loci were amplified by polymerase chain reaction (PCR) using a Veriti thermal cycler (Applied Biosystems, Foster City, CA, USA) with a total volume of 10 µL per reaction (containing 10 ng of genomic DNA, 1× buffer, 210 µM of each dNTP, 1.5 mM MgCl 2 , 0.16 µM forward primer and M13 (FAM or NED) broth [23], 0.32 µM reverse primer, 1.05 U Taq DNA polymerase (Invitrogen, Carlsbad, CA, USA), and 3.49 µL ultrapure water.…”