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Genotyping multidrug resistance gene-1, useful for assessing doses of pharmaceuticals, by mass spectrometric analysis of primer extension products

机译:通过对引物延伸产物进行质谱分析,对多药耐药基因-1进行基因分型,可用于评估药物剂量

摘要

Method for genotyping the MDR-1 (multidrug resistance-1) gene by mass spectrometric detection of the mutational status at some or all of 16 point mutations (single nucleotide polymorphism; SNPs). The sequences around all these mutations (coding and non-coding strands) are reproduced as sequences (1)-(32). Independent claims are also included for the following: (a) chemical package used to process samples for the new method comprising at least the primer for selective amplification of a DNA segment surrounding an SNP, reagents for primer extension and a mixture of terminating and non-terminating nucleotide triphosphates (NTPs); (b) point mutations defined by sequences (1)-(32); and (c) oligonucleotides, sequences (33)-(64), given in the specification, as attachment sites for primers in a mutation-dependent primer extension process for analysis of SNP.
机译:通过质谱检测16个点突变中的一些或全部(单核苷酸多态性; SNP)的突变状态对MDR-1(耐多药-1)基因进行基因分型的方法。所有这些突变周围的序列(编码链和非编码链)被复制为序列(1)-(32)。还包括以下方面的独立权利要求:(a)用于处理新方法样品的化学包装,该化学包装至少包括用于选择性扩增围绕SNP的DNA片段的引物,用于引物延伸的试剂以及终止和非杂交的混合物终止核苷酸三磷酸(NTPs); (b)由序列(1)-(32)定义的点突变; (c)本说明书中给出的寡核苷酸,序列(33)-(64),作为用于分析SNP的突变依赖性引物延伸过程中引物的附着位点。

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