电泳分离基质中DNA分级阶梯的相互比较及其对d1s80位点准确分型的潜力。

M C Kline, J W Redman, D J Reeder, D L Duewer
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引用次数: 0

摘要

典型的pcr扩增DNA片段的100-1,000碱基对大小需要高分辨率的电泳凝胶,以充分表征样品之间的微小差异。我们研究了一些商业施胶梯在三类分离系统中的行为:具有不连续缓冲液的聚丙烯酰胺、具有连续缓冲液的专有丙烯酰胺和具有连续缓冲液的琼脂糖类材料。使用供应商提供的标称梯架组件基对尺寸,所测试的梯架在这些系统中都没有充分的表现。在用等位基因阶梯校正后(用等位基因/基质特异性表观尺寸的最小二乘估计取代标称尺寸值),所有的阶梯都成功地分型了d1s80等位基因。一些阶梯和矩阵在质量上优于其他的。没有一个梯子被证明总是比其他梯子好;具有核糖修饰剂的聚丙烯酰胺凝胶在本研究中提供了最精确的结果。必须使用适当校准的电泳表观尺寸,以便在实验室之间有效地交换结果。适当的等位基因阶梯或已知等位基因的定义良好的子集可以作为校准系统。
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Intercomparison of DNA sizing ladders in electrophoretic separation matrices and their potential for accurate typing of the D1S8O locus.

The 100-1,000 basepair size typical of PCR-amplified DNA fragments demands high resolution electrophoretic gels for the adequate characterization of small differences among samples. We have studied the behavior of a number of commercial sizing ladders in three classes of separation systems: polyacrylamides with discontinuous buffer, proprietary acrylamides with continuous buffer, and agarose-like materials with continuous buffer. None of the ladders examined perform adequately in any of these systems using vendor-supplied nominal ladder component basepair sizes. All ladders successfully typed D1S8O alleles after calibration with the allelic ladder (replacing the nominal size values with the least squares estimate of allele/matrix-specific apparent sizes). Some ladders and matrices are qualitatively better than others. No one ladder proved consistently better than others; a polyacrylamide gel with ribose modifier provided the most precise results in this study. Appropriately calibrated electrophoretic apparent sizes must be used for results to be validly exchanged among laboratories. Appropriate allelic ladders or a well defined subset of known alleles can serve as the calibration system.

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Discontinuous electrophoresis revisited: a review of the process. The evaluation of fast purification methods for preparing polymerase chain reaction (PCR) products for capillary electrophoresis analysis. The use of a new gel matrix for the separation of DNA fragments: a comparison study between slab gel electrophoresis and capillary electrophoresis. DNA sequencing by capillary electrophoresis with a hydroxyethylcellulose sieving buffer. The distribution of F13A subtypes in four populations using agarose isoelectric focusing and Western Blot detection.
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