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Capillary electrophoresis with laser-induced fluorescence detection for fast and reliable apolipoprotein E genotyping

机译:毛细管电泳和激光诱导荧光检测,用于快速可靠的载脂蛋白E基因分型

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摘要

The use of capillary electrophoresis (CE) with laser-induced fluorescence (LIF) detection for the rapid determination of apolipoprotein E (apoE) genotypes was studied. High resolution and sensitive detection of the concerned DNA restriction fragments was achieved using CE buffers with hydroxypropylmethylcellulose (HPMC) as sieving polymer and ethidium bromide (EB) as fluorescent intercalating agent. In order to achieve adequate resolutions in short analysis times, parameters such as concentration of HPMC and EB, separation voltage, and length and coating of the capillary were evaluated. Using a separation buffer with 0.8% (w/w) HPMC and 7 μM EB, characteristic DNA-fragment profiles could be obtained for all common apoE genotypes at an overall rate of ten samples per hour. The method allows direct injection of untreated PCR samples and the use of standard fused-silica capillaries which are effectively coated following a short, one-step rinse procedure. With a simple computerized algorithm based on migration-time ratios for pattern assignment, highly reliable apoE genotyping was achieved. Overall, in terms of speed, ease of use and objectivity the presented method provides a significant improvement over previously reported CE-based procedures for apoE genotyping.
机译:研究了毛细管电泳(CE)和激光诱导荧光(LIF)检测技术在快速测定载脂蛋白E(apoE)基因型中的应用。使用CE缓冲液(羟丙基甲基纤维素(HPMC)作为筛分聚合物,溴化乙锭(EB)作为荧光嵌入剂)可实现对相关DNA限制性片段的高分辨率和灵敏检测。为了在短的分析时间内获得足够的分辨率,评估了诸如HPMC和EB的浓度,分离电压以及毛细管的长度和涂层等参数。使用具有0.8%(w / w)HPMC和7μMEB的分离缓冲液,可以获得所有常见apoE基因型的特征性DNA片段图谱,每小时的总采样率为10个样品。该方法可直接注入未经处理的PCR样品,并使用标准的熔融石英毛细管,这些毛细管在短短的一步冲洗程序后即可有效涂覆。使用基于迁移时间比率的简单计算机算法进行模式分配,可以实现高度可靠的apoE基因分型。总体而言,就速度,易用性和客观性而言,本方法相对于先前报道的基于ApoE基因分型的基于CE的程序提供了重大改进。

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