High-Resolution Detection of PCR Products from a Microsatellite Marker Using a Nonradioisotopic Technique

Debomoy K. Lahiri , Aiwu Zhang , John I. Nurnberger Jr.
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引用次数: 28

Abstract

We report a safe, rapid, and economical method for polymerase chain reaction (PCR)-based genotype analysis using a microsatellite marker specific for the human chromosome 18 locus, D18S53. This method does not involve radioisotopes and makes use of ethidium bromide fluorescence to detect PCR products. Our method enables direct analysis and easy detection of PCR products on nondenaturing polyacrylamide gels. The genotyping using this method can be scaled up to 100 samples at one time by adding a step of “double loading” of samples in a single sequencing size gel. We could resolve PCR products and DNA fragments, differing in size by only 2 bp, in the range of 150–200 bp by a 7% nondenaturing polyacrylamide gel. This technique can be applied for population-based genomic screening and linkage analysis.

利用非放射性同位素技术高分辨率检测微卫星标记的PCR产物
我们报道了一种安全、快速、经济的基于聚合酶链反应(PCR)的基因型分析方法,该方法使用人类18号染色体位点D18S53特异性微卫星标记。该方法不涉及放射性同位素,利用溴化乙啶荧光检测PCR产物。我们的方法能够在非变性聚丙烯酰胺凝胶上直接分析和轻松检测PCR产物。通过在单个测序大小的凝胶中添加样品的“双加载”步骤,使用该方法的基因分型可以一次扩展到100个样品。我们可以用7%的非变性聚丙烯酰胺凝胶来解析PCR产物和DNA片段,大小仅相差2bp,范围在150-200 bp之间。该技术可用于基于人群的基因组筛选和连锁分析。
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