PCR mixtures shall contain buffer (500 mM KCl, 100 mM Tris/HCl [pH 9,0 at 25 °C] and 1 % Triton® X-100), 2,5 mM MgCl2, 0,2 mM dNTP mix, 1 μM forward and reverse primers, 0,02 units μl– 1 Taq DNA polymerase, and 10 to100 ng of extracted DNA.
PCR-mengsels bevatten buffer (500 mM KCl, 100 mM Tris/HCl [pH 9,0 bij 25 °C] en 1 % Triton® X-100), 2,5 mM MgCl2, 0,2 mM dNTP-mengsel, 1 μM forward en reverse primers, 0,02 eenheden μl– 1 Taq DNA polymerase, en 10 tot 100 ng geëxtraheerd DNA.