Klintschar M
Institut für Gerichtliche Medizin, University of Graz, Austria.
Int J Legal Med. 1995;108(3):162-4. doi: 10.1007/BF01844830.
The short tandem repeat system FES/FPS was amplified by the polymerase chain reaction (PCR) in 211 unrelated Austrians and analysed by horizontal, non-denaturing electrophoresis. The allele distribution was in Hardy-Weinberg equilibrium. No mutations were found in 25 families (50 meioses). The mean exclusion chance was 0.49, the discriminating power 0.86 and the heterozygosity rate 74.4%. Amplification could be achieved with as little as 100 pg of high molecular weight DNA, which could be reduced to 75 pg by using 32 instead of 30 cycles. By reamplifying 1 microliter for another 15 cycles, the threshold could be reduced to less than 20 pg. In a degradation experiment DNA extracted from bloodstains stored for up to 24 days in a moist chamber and DNA boiled for up to 18 min could be amplified.
采用聚合酶链反应(PCR)对211名无亲缘关系的奥地利人进行短串联重复序列系统FES/FPS扩增,并通过水平非变性电泳进行分析。等位基因分布符合哈迪-温伯格平衡。在25个家系(50个减数分裂)中未发现突变。平均排除概率为0.49,鉴别能力为0.86,杂合率为74.4%。使用低至100 pg的高分子量DNA即可实现扩增,通过将循环次数从30次改为32次,可将所需DNA量降至75 pg。通过对1微升样本再进行15次循环扩增,阈值可降至20 pg以下。在一项降解实验中,从在潮湿环境中保存长达24天的血迹中提取的DNA以及煮沸长达18分钟的DNA均可实现扩增。