The rbcL regions were amplified in a 20L reaction mixture which included 1× Taq reaction buffer (UBI Life Sciences), 3mM MgCl2, 0.2mM dNTPs, 0.4M each primer, 0.63U Taq (UBI Life Sciences), and approximately 2 ng DNA.
TherbcL regions were amplified in a 20L reaction mixture whichincluded 1× Taq reaction buffer (UBI Life Sciences), 3mM MgCl2,0.2mM dNTPs, 0.4M each primer, 0.63U Taq (UBI Life Sciences),and approximately 2 ng DNA.