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DNA hybridization assays using temperature gradient focusing and peptide nucleic acids

机译:使用温度梯度聚焦和肽核酸的DNA杂交测定

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摘要

Two types of DNA hybridization assays are demonstrated with temperature gradient focusing (TGF) and peptide nucleic acids (PNAs). In TGF, the application of a controlled temperature gradient along the length of a microchannel filled with an appropriate temperature-dependent buffer results in the formation of a gradient in both the electric field and electrophoretic velocity. Ionic species move in this gradient and concentrate at a unique point where the total velocity sums to zero. The first assay is a mixing assay in which PNA is allowed to flow through spatially focused DNA targets within a capillary. The second assay detects single base pair mutations (SBPM) by monitoring the fluorescence intensity of PNA/DNA duplexes as a function of temperature within the capillary. The SBPM analysis can be performed in less than 5 min with 100-fold more dilute analyte compared to conventional UV melting measurements.
机译:用温度梯度聚焦(TGF)和肽核酸(PNA)证明了两种类型的DNA杂交测定。在TGF中,沿着填充有适当温度依赖性缓冲液的微通道的长度施加受控的温度梯度会导致电场和电泳速度均形成梯度。离子种类以该梯度移动并集中在总速度总和为零的唯一点。第一种测定是混合测定,其中允许PNA穿过毛细管内的空间聚焦DNA靶。第二种检测方法是通过监测PNA / DNA双链体的荧光强度与毛细管内温度的函数关系来检测单碱基对突变(SBPM)。与传统的UV熔融测量相比,SBPM分析可以在不到5分钟的时间内用100倍的稀分析物进行。

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