Suppr超能文献

PowerPlex(®) 21系统的发育验证

Developmental validation of the PowerPlex(®) 21 System.

作者信息

Ensenberger Martin G, Hill Carolyn R, McLaren Robert S, Sprecher Cynthia J, Storts Douglas R

机构信息

Promega Corporation, 2800 Woods Hollow Road, Madison, WI 53711, United States.

National Institute of Standards and Technology, 100 Bureau Drive, M/S 8312, Gaithersburg, MD 20899, United States.

出版信息

Forensic Sci Int Genet. 2014 Mar;9:169-78. doi: 10.1016/j.fsigen.2013.12.005. Epub 2013 Dec 24.

Abstract

The PowerPlex(®) 21 System is a STR multiplex that has been optimized for casework samples while still being capable of database workflows including direct amplification. The loci included in the multiplex offer increasing overlap with core loci used in different countries and regions throughout the world. The PowerPlex(®) 21 System contains D1S1656, D2S1338, D3S1358, D5S818, D6S1043, D7S820, D8S1179, D12S391, D13S317, D16S539, D18S51, D19S433, D21S11, Amelogenin, CSF1PO, FGA, Penta D, Penta E, TH01, TPOX, and vWA. These loci represent all 13 core CODIS loci in addition to loci commonly used in Asia and Europe. A developmental validation study was completed to document performance capabilities and limitations of the PowerPlex(®) 21 System. Data from this validation work served as the basis for the following conclusions: genotyping of single-source samples was reliable across a range of template DNA concentrations with >95% alleles called at 50 pg. Direct amplification of samples from FTA(®) storage cards was successfully performed using the reagents provided with the system and modified cycling protocols provided in the technical manual. Mixture analysis showed that over 95% of minor alleles were detected at 1:9 ratios. Reaction conditions including volume and annealing temperature as well as the concentrations of primers, DNA polymerase, magnesium, and Master Mix were shown to be optimal and able to withstand moderate variations without affecting system performance. Reproducible results were generated by different users at different sites. Finally, concordance studies showed consistent results when comparing the PowerPlex(®) 21 System with other commercially available STR-genotyping systems.

摘要

PowerPlex(®) 21系统是一种短串联重复序列(STR)复合扩增体系,已针对法医案件样本进行了优化,同时仍能够用于包括直接扩增在内的数据库工作流程。该复合扩增体系中的基因座与全球不同国家和地区使用的核心基因座的重叠度不断增加。PowerPlex(®) 21系统包含D1S1656、D2S1338、D3S1358、D5S818、D6S1043、D7S820、D8S1179、D12S391、D13S317、D16S539、D18S51、D19S433、D21S11、牙釉蛋白、CSF1PO、FGA、五核苷酸D、五核苷酸E、TH01、TPOX和vWA。这些基因座除了包括亚洲和欧洲常用的基因座外,还代表了所有13个核心联合DNA索引系统(CODIS)基因座。已完成一项开发验证研究,以记录PowerPlex(®) 21系统的性能能力和局限性。该验证工作的数据作为以下结论的依据:在一系列模板DNA浓度范围内,单一样本的基因分型可靠,在50 pg时等位基因检出率>95%。使用该系统提供的试剂和技术手册中提供的改良循环方案,成功地对来自FTA(®)储存卡的样本进行了直接扩增。混合分析表明,在1:9的比例下,超过95%的次要等位基因能够被检测到。反应条件,包括体积、退火温度以及引物、DNA聚合酶、镁和预混液的浓度,显示为最佳状态,并且能够承受适度变化而不影响系统性能。不同地点的不同用户产生了可重复的结果。最后,一致性研究表明,将PowerPlex(®) 21系统与其他市售STR基因分型系统进行比较时,结果一致。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验