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METHOD AND COMPOSITION FOR QUICK MULTIPLEX AMPLIFICATION OF STR GENE LOCUS

机译:STR基因座快速多重扩增的方法和组成

摘要

To provide a method for amplifying multiplex polymerase chain reaction (PCR) of a short tandem repeat (STR) gene locus that can be used for quickly generating a highly specific STR profile from target nucleic acid.SOLUTION: A method for detecting the presence of at least eight different single-nucleotide polymorphisms (SNPs) in a sample containing nucleic acid, in which the SNPs are detected by: (a) bringing the sample into contact with at least eight unlabeled primers in solution under the condition that hybridization between the primers and the nucleic acid in the sample is enabled; (b) performing labeling by a primer extension reaction, with one of at least eight different fluorescent dyes; and (c) detecting the primer extension product by a laser-induced fluorescence method by using a galvanometer of a step steering mode and a spectroscope equipped with a dispersion diffraction grating and a linear array detector.SELECTED DRAWING: None
机译:提供一种用于扩增短串联重复(STR)基因位点的多重聚合酶链反应(PCR)的方法,该方法可用于从靶核酸快速生成高度特异性的STR谱图。解决方案:一种检测at的存在的方法含有核酸的样品中至少有八种不同的单核苷酸多态性(SNP),可通过以下方法检测SNP:(a)使样品与溶液中至少八种未标记的引物接触,条件是引物与样品中的核酸被启用; (b)通过引物延伸反应用至少八种不同的荧光染料之一进行标记; (c)使用步进控制模式的检流计和配备有色散衍射光栅和线性阵列检测器的分光镜,通过激光诱导的荧光法检测引物延伸产物。

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