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骨密度遗传标记COL1a1 Sp1结合位点二态性的快速高效基因分型分析

Rapid and efficient genotype analysis of the COL1a1 Sp1 binding site dimorphism, a genetic marker for bone mineral density.

作者信息

Mirandola S, Sangalli A, Mottes M

机构信息

Section of Biology and Genetics, Dept. of Mother and Child, Biology and Genetics, University of Verona, Italy.

出版信息

Mol Cell Probes. 2002 Feb;16(1):73-5. doi: 10.1006/mcpr.2001.0401.

Abstract

A biallelic G/T polymorphism within the first intron of COL1A1 gene at a recognition site for the transcription factor Sp1 has been shown to be significantly related to bone mass and osteoporotic fracture. To date this polymorphism has been detected by conventional genomic DNA amplification followed by restriction enzyme digestion and polyacrylamide gel electrophoresis. We have designed a rapid and efficient genotyping method based on allele-specific polymerase chain reaction

摘要

已证明,位于转录因子Sp1识别位点的COL1A1基因第一内含子内的双等位基因G/T多态性与骨量和骨质疏松性骨折显著相关。迄今为止,这种多态性是通过常规基因组DNA扩增,然后进行限制性酶切和聚丙烯酰胺凝胶电泳来检测的。我们基于等位基因特异性聚合酶链反应设计了一种快速高效的基因分型方法。

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