首页> 外国专利> Haplotype Marker Single Base Variation and Uses thereof for the Functional Variation Analysis of Pregnan X Receptor Genes

Haplotype Marker Single Base Variation and Uses thereof for the Functional Variation Analysis of Pregnan X Receptor Genes

机译:单倍型标记单碱基变异及其在Pregnan X受体基因功能变异分析中的应用

摘要

A method for selecting htSNP of a genotype of PXR gene is provided to confirm the functional genotype of PXR gene discovered in the Asian which is similar to Korean genetic character easily by using a htSNP obtained with the SNP of the PXR gene of Korean. A method for selecting htSNP of a genotype of PXR gene comprises (1) a step for collecting the biological material from the human; (2) a step for extracting a nucleic acid from the collected sample of the step (1); (3) a step for performing PCR with a primer which amplifies the human PXR gene or its fraction by using a nucleic acid of the step (2) as a template; (4) a step for confirming the variation in the sequence of the PCR product obtained from the step (3); (5) a step for analyzing the haplotype in the sequence of the PCR product which exists variation in the step (4); and (6) a step for selecting htSNP by analyzing the sequence of the haplotype analyzed in the step (5) by using the SNP tagger software.
机译:提供一种选择PXR基因的基因型的htSNP的方法,以通过使用由韩国人的PXR基因的SNP获得的htSNP,容易地确认在亚洲发现的与韩国人的遗传特性相似的PXR基因的功能基因型。一种选择PXR基因型的htSNP的方法包括:(1)从人体内收集生物材料的步骤; (2)从步骤(1)的收集样品中提取核酸的步骤; (3)以步骤(2)的核酸为模板,用扩增人PXR基因或其片段的引物进行PCR的步骤。 (4)用于确认从步骤(3)得到的PCR产物的序列的变异的步骤。 (5)分析在步骤(4)中存在变异的PCR产物的序列中的单倍型的步骤; (6)通过使用SNP标记软件分析步骤(5)中分析的单倍型的序列来选择htSNP的步骤。

著录项

  • 公开/公告号KR101057129B1

    专利类型

  • 公开/公告日2011-08-16

    原文格式PDF

  • 申请/专利权人

    申请/专利号KR20070059247

  • 申请日2007-06-18

  • 分类号C12Q1/68;

  • 国家 KR

  • 入库时间 2022-08-21 17:49:55

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