Coticone Sulekha Rao, Oldroyd Nicola, Philips Heidi, Foxall Paul
Human Identification Group, Applied Biosystems, Foster City, CA 94404, USA.
Int J Legal Med. 2004 Aug;118(4):224-34. doi: 10.1007/s00414-004-0459-y. Epub 2004 May 15.
The AmpFISTR SEfiler kit co-amplifies 11 short tandem repeat loci including SE33 in a single multiplex. After establishing the optimum in primer titration studies, the primer concentrations of all loci in the multiplex were chosen such that the heterozygote peak height ratios of each of the loci were balanced. The combined primer set was then tested to determine the robustness of the multiplex under various conditions. Different MgCl(2) concentrations were evaluated to establish the optimum concentration for the multiplex. The amplification of the various loci in the multiplex was tested at several annealing temperatures (55-63 degrees C). Additionally, DNA from primates, non-primates and microorganisms were amplified to investigate the specificity of the kit. The stability of the AmpFISTR SEfiler kit was determined by addition of hematin, to simulate inhibition, and the use of degraded DNA. Population studies revealed a probability of identity of 6.47x10(-15) for African Americans and 7.46x10(-14) for US Caucasians. To assess the ability of the multiplex to analyze forensic samples, testing on blood, oral swabs and mixtures was performed. Based on the various studies, it was determined that the AmpFISTR SEfiler PCR amplification kit can be used to successfully analyze a variety of forensic, databasing and paternity samples.
AmpFISTR SEfiler试剂盒可在一次复合扩增中共同扩增11个短串联重复序列位点,包括SE33。在引物滴定研究中确定最佳条件后,选择复合扩增中所有位点的引物浓度,以使每个位点的杂合子峰高比达到平衡。然后对组合引物组进行测试,以确定该复合扩增在各种条件下的稳健性。评估了不同的MgCl₂浓度,以确定复合扩增的最佳浓度。在几个退火温度(55 - 63℃)下测试了复合扩增中各个位点的扩增情况。此外,对来自灵长类动物、非灵长类动物和微生物的DNA进行扩增,以研究该试剂盒的特异性。通过添加血红素模拟抑制作用并使用降解DNA来确定AmpFISTR SEfiler试剂盒的稳定性。群体研究表明,非裔美国人的个体识别概率为6.47×10⁻¹⁵,美国白人为7.46×10⁻¹⁴。为评估该复合扩增分析法医样本的能力,对血液、口腔拭子及混合样本进行了测试。基于各项研究,确定AmpFISTR SEfiler PCR扩增试剂盒可成功用于分析各种法医、数据库及亲子鉴定样本。