A chemiluminescence-based detection system for human DNA quantitation and restriction fragment length polymorphism (RFLP) analysis.

A M Giusti, B Budowle
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引用次数: 0

Abstract

A protocol for the chemiluminescent detection of restriction fragment length polymorphism (RFLP) profiles with the sensitivity of radioisotope-based detection systems is presented. RFLP profiles for the loci D2S44, D17S79, D1S7, D4S139, and D5S110 were obtained from ten nanograms of HaeIII-digested K562 DNA and 50 nanograms of human genomic DNA isolated from bloodstains. DNA is transferred to an amphoteric membrane using a neutral, high salt transfer procedure. Oligonucleotide probes directly conjugated to alkaline phosphatase are hybridized to the membranes, then the membranes are incubated with a substrate that emits light upon chemical cleavage by the alkaline phosphatase. Several variables were investigated to determine the optimum conditions for RFLP profile generation, among them transfer conditions, film selection, and exposure conditions. A chemiluminscent human DNA quantitation protocol, consistent with the RFLP detection protocol, is also presented.

基于化学发光的人类DNA定量和限制性片段长度多态性(RFLP)分析检测系统。
提出了一种具有放射性同位素检测系统灵敏度的限制性片段长度多态性(RFLP)化学发光检测方法。从10纳克haeiii酶切的K562 DNA和50纳克从血迹中分离的人类基因组DNA中获得了D2S44、D17S79、D1S7、D4S139和D5S110位点的RFLP图谱。DNA通过中性的高盐转移过程转移到两性膜上。将直接与碱性磷酸酶结合的寡核苷酸探针与膜杂交,然后将膜与碱性磷酸酶化学裂解时发光的底物孵育。研究了几个变量以确定RFLP剖面生成的最佳条件,其中包括转移条件、胶片选择和曝光条件。本文还提出了一种与RFLP检测方案一致的化学发光人类DNA定量方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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