Brilliant cresyl blue as a new red region fluorescent probe for determination of nucleic acids

被引:23
|
作者
Zheng, H
Chen, XL
Zhu, CQ
Li, DH
Chen, QY
Xu, JG [1 ]
机构
[1] Xiamen Univ, Dept Chem, Key Lab Analyt Sci MOE, Xiamen 361005, Peoples R China
[2] Anhui Normal Univ, Dept Chem, Wuhu 241000, Peoples R China
基金
中国国家自然科学基金;
关键词
red region fluorescence; nucleic acids; fluorometric method; brilliant cresyl blue (BCB);
D O I
10.1016/S0026-265X(00)00015-1
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A fluorescence quenching method was developed for determination of microamounts of nucleic acids by using brilliant cresyl blue (BCB) as a new red region fluorescent probe. In aqueous hexylmethylene tetramine solution, BCB showed maximum excitation and emission wavelengths at 626 and 670 nm, respectively, and the fluorescence of BCB could be greatly quenched by DNA (or RNA). Under optimal conditions, the calibration graphs are linear over the range of 0.02-0.80 mu g/ml for SM DNA and 0.25-1.5 mu g/ml for yeast RNA. The corresponding detection limits are 7 ng/ml for SM DNA and 25 ng/ml for yeast RNA, respectively. SM DNA can be determinated in the presence of 40% (w/w) RNA, and the relative standard deviation of six measurements is 2.5% for 500 ng/ml SM DNA. The result of the determination of golden staphylococcus DNA by this method was satisfactory. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:263 / 269
页数:7
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