Westring Christian G, Kristinsson Richard, Gilbert Dustin M, Danielson Phillip B
Department of Biological Sciences, University of Denver, 2190 E. Iliff Ave., Denver, CO 80208, USA.
J Forensic Sci. 2007 Sep;52(5):1035-43. doi: 10.1111/j.1556-4029.2007.00525.x. Epub 2007 Aug 6.
Accurate quantification of DNA samples is an important step in obtaining accurate and reproducible short tandem repeat (STR) profiles. Quantitative real-time-PCR has improved the speed and accuracy of DNA quantification over earlier methods, albeit at significantly greater cost per reaction. Here, the performance of reduced volume (10 microL) DNA quantification assays using the Quantifiler Human DNA Quantification Kit was evaluated using commercial standards and single source biological stains (e.g., venous blood, saliva, and semen). In addition, casework-type samples including those subjected to environmental contaminants containing PCR inhibitors and samples having undergone extensive DNA degradation were also quantified. The concentration of DNA in various forensic samples ranged from 0 to 2.9 ng/microL depending on sample source and/or environmental insult. Compared to full-scale reactions, reduced volume assays displayed equivalent to improved amplification efficiency and sample-to-sample reproducibility (+/-0.01-0.17 C(T FAM)). Furthermore, the use of data from reduced-scale Quantifiler reactions facilitated the accurate determination of the amount of sample DNA extract needed to generate quality STR profiles. The use of 10 microL-scale Quantifiler reaction volumes has the practical benefit of increasing the effective number of reactions per kit by 250%; thereby reducing the cost per assay by 60% while consuming less sample. This is particularly advantageous in cases of consumptive testing.
准确量化DNA样本是获得准确且可重复的短串联重复序列(STR)图谱的重要一步。相较于早期方法,定量实时聚合酶链反应(qPCR)提高了DNA定量的速度和准确性,尽管每个反应的成本显著更高。在此,我们使用商业标准品和单一来源生物污渍(如静脉血、唾液和精液)评估了使用Quantifiler人类DNA定量试剂盒进行的小体积(10微升)DNA定量分析的性能。此外,还对包括受到含有PCR抑制剂的环境污染物影响的样本以及经历大量DNA降解的样本等实际案件类型样本进行了定量分析。根据样本来源和/或环境损害情况,各种法医样本中的DNA浓度范围为0至2.9纳克/微升。与全量反应相比,小体积分析显示出同等至更高的扩增效率以及样本间的可重复性(±0.01 - 0.17 C(T FAM))。此外,使用小体积Quantifiler反应的数据有助于准确确定生成高质量STR图谱所需的样本DNA提取物的量。使用10微升规模的Quantifiler反应体积具有实际优势,可使每个试剂盒的有效反应数量增加250%;从而将每次分析的成本降低60%,同时消耗更少的样本。这在消耗性检测的情况下尤为有利。