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使用水溶性纸上的干唾液和发根,通过TaqMan PCR测定法直接检测单核苷酸多态性(SNP),无需提取DNA。

Direct detection of single nucleotide polymorphism (SNP) by the TaqMan PCR assay using dried saliva on water-soluble paper and hair-roots, without DNA extraction.

作者信息

Hayashida Mariko, Ota Tomoko, Ishii Minori, Iwao-Koizumi Kyoko, Murata Shigenori, Kinoshita Kenji

机构信息

School of Pharmaceutical Sciences, Mukogawa Women's University.

出版信息

Anal Sci. 2014;30(3):427-9. doi: 10.2116/analsci.30.427.

Abstract

We have developed a new method for directly using unprocessed biological specimens as templates for the TaqMan assay. DNA extraction and purification had been believed to be required for the assay, but our new method could avoid hindering fluorescence detection, even if the templates were used directly. Saliva was needed to be put on water-soluble paper and dried, and hairs were cut to be about 10 mm long. This method could reduce both the time and effort involved, and also the risk of contamination. It should prove to be very valuable for genetic diagnoses in various fields.

摘要

我们开发了一种新方法,可直接将未经处理的生物样本用作TaqMan检测的模板。此前人们认为该检测需要进行DNA提取和纯化,但我们的新方法即使直接使用模板也能避免妨碍荧光检测。唾液需置于水溶性纸上并干燥,毛发要剪成约10毫米长。这种方法可以减少所需的时间和精力,也降低了污染风险。它在各个领域的基因诊断中应该会被证明非常有价值。

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