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Multiplex Sets for the Amplification of Polymorphic Short Tandem Repeat Loci Silver Stain and Fluorescence Detection

机译:用于扩增多态性短串联重复基因座银染和荧光检测的多重集

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摘要

Multiplex PCR amplification systems were developed using well-characterized, polymorphic short tandem repeat (STR) loci. Eight loci utilized in the multiplex amplifications included HUMCSF1PO, HUMTPOX, HUMTH01, HUMVWFA31, HUMF13A01, HUMFESFPS, HUMBFXIII and HUMLIPOL. From this list, three or four non-overlapping loci were simultaneously amplified, separated by denaturing poly-acrylamide gel electrophoresis and visualized using silver stain or fluorescence detection. The multiplex PCR amplification systems offer 'a non-isotopic method for rapid, simple and accurate analysis of STR loci. This high-throughput method for DMA identification has immediate and valuable application in forensic analysis, paternity determination, tissue culture strain identification and bone marrow transplantation studies.
机译:使用表征良好的多态性短串联重复序列(STR)基因座开发了多重PCR扩增系统。多重扩增中使用的八个基因座包括HUMCSF1PO,HUMTPOX,HUMTH01,HUMVWFA31,HUMF13A01,HUMFESFPS,HUMBFXIII和HUMLIPOL。从该列表中,同时扩增三个或四个不重叠的基因座,通过变性聚丙烯酰胺凝胶电泳进行分离,并使用银染或荧光检测进行可视化。多重PCR扩增系统提供了一种用于快速,简单和准确分析STR基因座的非同位素方法。这种用于DMA识别的高通量方法在法医分析,亲子鉴定,组织培养菌株鉴定和骨髓移植研究中具有直接而有价值的应用。

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