首页> 外文期刊>Molecular and Cellular Probes: The Location, Diagnosis and Monitoring of Disease by Specific Molecules and Cell Lines >A rapid one-tube PCR method for simultaneously differentiating homozygotes and heterozygotes of the Sp1 binding site polymorphism in collagen type Ialpha1.
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A rapid one-tube PCR method for simultaneously differentiating homozygotes and heterozygotes of the Sp1 binding site polymorphism in collagen type Ialpha1.

机译:一种快速的单管PCR方法,用于同时区分Ialpha1型胶原Sp1结合位点多态性的纯合子和杂合子。

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摘要

Rapid detection of single-base changes is fundamental to molecular medicine. PCR amplification of specific alleles (PASA) has previously been used as a rapid method of genotyping single-nucleotide changes, but one reaction is required for each allele. This paper describes a Bidirectional PASA (Bi-PASA) method, which was developed to distinguish between homozygotes and heterozygotes in one PCR reaction. The method is tested using the Sp1 polymorphism in Collagen type Ialpha1. The results demonstrate that Bi-PASA is a simple and rapid method for detecting the zygosity of the polymorphism in a single PCR reaction.
机译:快速检测单碱基变化是分子医学的基础。先前已将特定等位基因(PASA)的PCR扩增用作对单核苷酸变化进行基因分型的快速方法,但每个等位基因都需要一个反应。本文介绍了一种双向PASA(Bi-PASA)方法,该方法旨在区分一个PCR反应中的纯合子和杂合子。使用I1型胶原蛋白中的Sp1多态性对该方法进行了测试。结果表明,Bi-PASA是在单个PCR反应中检测多态性的接合性的简单而快速的方法。

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