Morozkin Evgeniy S, Laktionov Pavel P, Rykova Elena Y, Vlassov Valentin V
Institute of Bioorganic Chemistry, Siberian Division, Russian Academy of Sciences, 8 Lavrentier Ave., 630090 Novosibirsk, Russia.
Anal Biochem. 2003 Nov 1;322(1):48-50. doi: 10.1016/j.ab.2003.07.009.
A fluorescence-based method for quantitative determination of RNA and DNA in probes containing both nucleic acids has been developed. The total concentration of nucleic acids is determined using SYBR Green II dye under conditions providing independent binding of the fluorophore with DNA and RNA. The concentration of DNA is specifically measured using the Hoechst 33258 dye and the RNA concentration is calculated from these data. The procedure allows for accurate determination of DNA concentration in the range 10-1000 ng/ml in the presence of 200-fold excess of RNA and determination of RNA concentrations in the range 10-1000 ng/ml in the presence of large excess of DNA. An absence of the treatment of mixed samples with RNase-free DNase I provides rapid, reproducible, and accurate RNA quantification.
已开发出一种基于荧光的方法,用于定量测定同时含有核酸的探针中的RNA和DNA。在荧光团与DNA和RNA独立结合的条件下,使用SYBR Green II染料测定核酸的总浓度。使用Hoechst 33258染料特异性测量DNA浓度,并根据这些数据计算RNA浓度。该方法能够在存在200倍过量RNA的情况下,准确测定浓度范围为10-1000 ng/ml的DNA浓度;在存在大量过量DNA的情况下,准确测定浓度范围为10-1000 ng/ml的RNA浓度。无需用无RNase的DNase I处理混合样品,即可实现快速、可重复且准确的RNA定量。