The PCR products were analyzed by electrophoresis in agarose gels stained with ethidium bromide.
扩增产物用琼脂糖凝胶电泳, 溴化乙锭染色检测。
KI quenching and competitive binding between MnSchiff base and ethidium bromide for DNA were studied.
其紫外可见光谱亦有明显的减色效应和微紫移。
Owing to these properties, a continuous kinetic assay for RNAcleaving deoxyribozymes could exploit ethidium bromide as an extrinsic fluorescent probe.
大量存在的荧光团还可能影响脱氧核酶催化反应的动力学。
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