Day I N, Humphries S E, Richards S, Norton D, Reid M
Dept. of Medicine, University College London Medical School, Rayne Institute, UK.
Biotechniques. 1995 Nov;19(5):830-5.
Genotyping (typing of genetic variation) typically involves PCR followed by an allele-specific oligonucleotide-binding assay, restriction enzyme digest or direct check of the outcome of a PCR designed to distinguish genotype. Electrophoresis can resolve "bound" from "free" oligonucleotide, as well as resolve PCR fragments and digests, but it is traditionally regarded as cumbersome and laborious in comparison with solution assays. Here we describe simple horizontal polyacrylamide gels which can receive a 96-well array of samples directly, which can be stacked in tanks and which are bound to a robust support of glass. The line of electrophoresis is on a 71.6 degree diagonal relative to the columns of the array (microplate array diagonal gel electrophoresis [MADGE]). Several thousand reactions can conveniently be analyzed in a shoebox-sized apparatus in a couple of hours. High resolution is achieved in the range of 20-1000 bp, information processing is simplified and automation is possible.
基因分型(对基因变异进行分型)通常包括聚合酶链反应(PCR),随后进行等位基因特异性寡核苷酸结合分析、限制性内切酶消化或直接检查用于区分基因型的PCR结果。电泳可以区分“结合的”和“游离的”寡核苷酸,还能分离PCR片段和消化产物,但传统上与溶液分析相比,它被认为既繁琐又费力。在此,我们描述了一种简单的水平聚丙烯酰胺凝胶,它可以直接容纳96孔阵列的样品,可以堆叠在电泳槽中,并固定在坚固的玻璃支撑物上。电泳线相对于阵列的列呈71.6度对角线(微孔板阵列对角线凝胶电泳 [MADGE])。在鞋盒大小的仪器中,几个小时内就可以方便地分析数千个反应。在20 - 1000 bp范围内可实现高分辨率,信息处理得到简化,并且可以实现自动化。