Xiang Hai-yan, Chen Xiao-ming, Zhou Di-wu
Printed Circuit Board Factory, Zhuzhou Electric Locomotive Institute, Zhuzhou 412001, China.
Guang Pu Xue Yu Guang Pu Fen Xi. 2002 Dec;22(6):1051-3.
The method is based on the enhancement effect of the resonance light-scattering (RLS) of pararosaniline by DNA. In the pH rang of 0.5-1.5, the enhanced intensity of pararosaniline RLS at 355 nm is proportional to the concentration of DNA in the rang of 0.20-15 micrograms.mL-1. The detection limit is 36 ng.mL-1. This method is simple, rapid and has been applied satisfactorily to the determination of DNA in mixed samples.
该方法基于DNA对副品红共振光散射(RLS)的增强作用。在0.5 - 1.5的pH范围内,355nm处副品红RLS的增强强度与0.20 - 15微克·毫升⁻¹范围内的DNA浓度成正比。检测限为36纳克·毫升⁻¹。该方法简单、快速,已成功应用于混合样品中DNA的测定。