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首页> 外文期刊>Spectrochimica acta, Part A. Molecular and biomolecular spectroscopy >Micro-determination of nucleic acids with a simple probe manganese chloride based on the fine enhanced resonance light scattering
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Micro-determination of nucleic acids with a simple probe manganese chloride based on the fine enhanced resonance light scattering

机译:基于精细的增强共振光散射,使用简单的氯化锰探针对核酸进行微测定

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Manganese chloride can form large particles with nucleic acids by electrostatic forces, which results in strong enhancement of resonance light scattering (RLS) signals. Based on this phenomenon, a novel and very simple assay of DNA was established. The work conditions have been investigated including the concentration of probe, the acidity of solution, the effect of ionic strength and the selectivity. In acidic solution, the enhanced RLS intensity at 389.5 nm was proportional to the concentration of nucleic acids in the range 0.05-10.0 mu g ml(-1) for both ctDNA and fsDNA and 1.0-10.0 mu g ml(-1) for yRNA. The limits of detection (LOD, 3 sigma) were 0.17, 0.13 and 0.53 ng ml(-1) for ctDNA, fsDNA and yRNA, respectively. Synthetic samples were determined satisfactorily. (C) 2006 Elsevier B.V. All rights reserved.
机译:氯化锰可以通过静电力与核酸形成大颗粒,从而大大增强了共振光散射(RLS)信号。基于这种现象,建立了一种新颖且非常简单的DNA检测方法。研究了工作条件,包括探针浓度,溶液的酸度,离子强度的影响和选择性。在酸性溶液中,在389.5 nm处增强的RLS强度与ctDNA和fsDNA的0.05-10.0μg ml(-1)和yRNA的1.0-10.0μg ml(-1)范围内的核酸浓度成正比。 。 ctDNA,fsDNA和yRNA的检出限(LOD,3 sigma)分别为0.17、0.13和0.53 ng ml(-1)。合成样品的测定令人满意。 (C)2006 Elsevier B.V.保留所有权利。

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