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通过直接应用PCR-RFLP技术对干血样进行酒精和乙醛脱氢酶基因多态性基因分型,无需提取DNA。

Genotyping of polymorphisms in alcohol and aldehyde dehydrogenase genes by direct application of PCR-RFLP on dried blood without DNA extraction.

作者信息

Hayashida Mariko, Iwao-Koizumi Kyoko, Murata Shigenori, Yokoyama Akira, Kinoshita Kenji

机构信息

School of Pharmaceutical Sciences, Mukogawa Women's University, Koshien, Nishinomiya 663-8179, Japan.

出版信息

Anal Sci. 2010;26(4):503-5. doi: 10.2116/analsci.26.503.

Abstract

We have developed a simple, labor-saving, inexpensive, and rapid single nucleotide polymorphism (SNP) genotyping method that works directly on whole human blood. This single-tube genotyping method was used to successfully and reliably genotype ADH1B and ALDH2 polymorphisms without DNA isolation using a 1.2-mm disc of dried blood and the KOD FX PCR enzyme kit. SNP genotyping was performed by a polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. In addition to the labor and expense advantages, the possibility of sample contamination was considerably decreased, since the DNA extraction step was eliminated. In the post-genome era, a simple and inexpensive method for diagnostic analysis is in high demand, and this method will be very useful for genetic diagnoses in biological and medical laboratories.

摘要

我们开发了一种简单、省力、廉价且快速的单核苷酸多态性(SNP)基因分型方法,该方法可直接用于全血样本。这种单管基因分型方法通过使用1.2毫米干血片和KOD FX PCR酶试剂盒,无需进行DNA提取,就能成功且可靠地对ADH1B和ALDH2多态性进行基因分型。SNP基因分型通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法进行。除了省力和成本低的优点外,由于省去了DNA提取步骤,样本污染的可能性也大大降低。在后基因组时代,对简单且廉价的诊断分析方法需求很高,该方法将对生物和医学实验室的基因诊断非常有用。

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