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首页> 外文期刊>Microchimica Acta >The Fluorescent Reaction Between Quinaldine Red and Nucleic Acids and its Application to Fluorescent Assay of DNA and RNA
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The Fluorescent Reaction Between Quinaldine Red and Nucleic Acids and its Application to Fluorescent Assay of DNA and RNA

机译:喹诺丁红与核酸之间的荧光反应及其在DNA和RNA荧光测定中的应用

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摘要

The reaction between quinaldine red (QR) and nucleic acids was studied. The free QR alone has no fluorescence in solution. However, it becomes fluorescent after binding to nucleic acids, giving maximum emission at 607 nm with maximum excitation at 557 nm. Maximum fluorescence intensity is produced in the pH range of 3.2–3.6. Based on the fluorescent reactions, a novel fluorometric method was developed for rapid determination of nucleic acids using QR as the fluorescent probe. Under optimal conditions, the calibration graphs were linear in the range of 0–30.0 µg mL−1 for CT DNA and 0–20.0 µg mL−1 for yeast RNA. The limits of detection were 38 ng mL−1 for CT DNA and 142 ng mL−1 for yeast RNA. Four synthetic samples were determined with satisfaction.
机译:研究了奎尼丁红(QR)与核酸之间的反应。仅游离QR溶液中无荧光。但是,它在与核酸结合后变成荧光,在607 nm处发出最大发射,在557 nm处产生最大激发。在3.2-3.6的pH范围内产生最大的荧光强度。基于荧光反应,开发了一种新颖的荧光法,可将QR作为荧光探针快速测定核酸。在最佳条件下,CT DNA和酵母RNA的校正图在0–30.0 µg mL-1 范围内呈线性。 CT DNA的检出限为38 ng mL-1 ,酵母RNA的检出限为142 ng mL-1 。满意地确定了四个合成样品。

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  • 来源
    《Microchimica Acta》 |2003年第1期|33-37|共5页
  • 作者单位

    Department of Chemistry Nankai University Tianjin 300071 P.R. China;

    Department of Chemistry Nankai University Tianjin 300071 P.R. China;

    Department of Chemistry Nankai University Tianjin 300071 P.R. China;

    Department of Chemistry Nankai University Tianjin 300071 P.R. China;

    College of Chemistry and Life Science Guangxi Normal University Guilin 541004 P.R. China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Key words: Quinaldine red; DNA; RNA; determination.;

    机译:关键字:奎奴尔丁红;脱氧核糖核酸;RNA;判定。;

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