产品性状

Null,without related properties.

质量标准

PCR Suitability
dNTP Mix was tested at a final concentration of 200 μM in a reaction mixture containing10 mM Trizma?-HCl, pH 8.3 at 25 °C, 50 mM KCl, 1.5 mM MgCl2,
0.001% (w/v) gelatin, primers defining an approximately 500 base pair region of λ DNA at 1.0 μM each, λ DNA template at 1 ng/100 μl, and Taq DNA polymerase at 2.5 units/100 μl. The reaction underwent 25 cycles of 94 °C to denature the double stranded DNA, 55 °C to anneal the DNA segments, and 72 °C to extend the DNA segments. A single band of approximately 500 base pairs was visualized following electrophoresis of the reaction product in a 1.5% agarose gel.