Lins A M, Sprecher C J, Puers C, Schumm J W
Promega Corporation, Madison, WI, USA.
Biotechniques. 1996 May;20(5):882-9. doi: 10.2144/96205rr01.
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 polyacrylamide 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 DNA identification has immediate and valuable application in forensic analysis, paternity determination, tissue culture strain identification and bone marrow transplantation studies.
多重PCR扩增系统是利用特征明确的多态性短串联重复序列(STR)位点开发的。多重扩增中使用的八个位点包括HUMCSF1PO、HUMTPOX、HUMTH01、HUMVWFA31、HUMF13A01、HUMFESFPS、HUMBFXIII和HUMLIPOL。从这个列表中,同时扩增三到四个不重叠的位点,通过变性聚丙烯酰胺凝胶电泳分离,并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非同位素方法,用于快速、简单和准确地分析STR位点。这种用于DNA鉴定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且有价值的应用。