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首页> 外文期刊>Mikrochimica Acta: An International Journal for Physical and Chemical Methods of Analysis >Double signal enhancement strategy based on rolling circle amplification and photoinduced electron transfer for ultrasensitive fluorometric detection of methylated DNA
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Double signal enhancement strategy based on rolling circle amplification and photoinduced electron transfer for ultrasensitive fluorometric detection of methylated DNA

机译:基于滚动圆扩增的双信号增强策略和光致电子转移,用于甲基化DNA的超细荧光检测

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摘要

The authors describe a novel assay for the detection of methylated DNA site. Rolling circle amplification and CdSe/ZnS quantum dots with high fluorescence efficiency are applied in this method. The CdSe/ZnS quantum dots act as electron donors, and hemin and oxygen (derived from hydrogen peroxide act as acceptors in photoinduced electron transfer. The assay, best performed at excitation/emission peaks of 450/620 nm, is sensitive and specific. Fluorometric response is linear in the 1 pM to 100 nM DNA concentration range, and the lowest detectable concentration of methylated DNA is 142 fM (S/N = 3). The method is capable of recognizing 0.01% methylated DNA in a mixture of methylated/unmethylated DNA.
机译:作者描述了用于检测甲基化DNA位点的新型测定。 在该方法中应用滚动圆扩增和具有高荧光效率的量子点。 CDSE / ZnS量子点作为电子给体,血红素和氧气(来自过氧化氢作为受光电电子转移中的受体。在450/620nm的激发/发射峰时的最佳测定是敏感和特异性的。荧光 响应在1pP至100nm DNA浓度范围内是线性的,并且最低可检测的甲基化DNA浓度为142 fm(s / n = 3)。该方法能够在甲基化/未甲基化的混合物中识别0.01%甲基化DNA 脱氧核糖核酸。

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