Collins Patrick J, Hennessy Lori K, Leibelt Craig S, Roby Rhonda K, Reeder Dennis J, Foxall Paul A
Human Identification Group, Applied Biosystems, Foster City, CA 94404, USA.
J Forensic Sci. 2004 Nov;49(6):1265-77.
Analysis of length polymorphism at short tandem repeat (STR) loci utilizing the polymerase chain reaction (PCR) process has proven to be an ideal assay for human identification purposes. The short length of STR loci coupled with the amplification of target sequence through PCR allows for a robust, sensitive, and specific assay for highly polymorphic markers. A multiplex containing fifteen STR loci plus the gender-determining locus Amelogenin was developed to provide a single amplification/detection of all CODIS (Combined DNA Index System) STR loci (CSF1PO, D3S1358, D5S818, D7S820, D8S1179, D13S317, D16S539, D18S51, D21S11, FGA, TH01, TPOX, and vWA) as well as two internationally-accepted STRs (D2S1338 and D19S433). By incorporating five-dye fragment analysis technology and non-nucleotide linkers, previously optimized AmpFlSTR kit primer sequences have been maintained. This kit has been developed in accordance with the standards of the forensic community as defined by the DNA Advisory Board. Validation studies were performed to include developmental validation, and the results support the use of the AmpFlSTR Identifiler PCR Amplification Kit for human identity and parentage testing.
利用聚合酶链反应(PCR)对短串联重复序列(STR)位点的长度多态性进行分析,已被证明是用于人类身份鉴定的理想检测方法。STR位点的短长度加上通过PCR对靶序列的扩增,使得对高度多态性标记物进行稳健、灵敏且特异的检测成为可能。开发了一种包含15个STR位点以及性别决定位点牙釉蛋白(Amelogenin)的复合扩增体系,以对所有联合DNA索引系统(CODIS)的STR位点(CSF1PO、D3S1358、D5S818、D7S820、D8S1179、D13S317、D16S539、D18S51、D21S11、FGA、TH01、TPOX和vWA)以及两个国际认可的STR(D2S1338和D19S433)进行单一扩增/检测。通过采用五染料片段分析技术和非核苷酸接头,先前优化的AmpFlSTR试剂盒引物序列得以保留。该试剂盒是根据DNA咨询委员会定义的法医界标准开发的。进行了包括方法学验证在内的验证研究,结果支持使用AmpFlSTR Identifiler PCR扩增试剂盒进行人类身份鉴定和亲子鉴定。