首页> 外国专利> Multiplex PCR for simultaneous quantitation of human nuclear, mitochondrial, and male Y-chromosome DNA

Multiplex PCR for simultaneous quantitation of human nuclear, mitochondrial, and male Y-chromosome DNA

机译:多重PCR同时定量人类核,线粒体和雄性Y染色体DNA

摘要

A comprehensive set of human specific, target specific, multiplex PCR assays for DNA quantitation is provided. Our duplex qPCR for nDNA/mtDNA had a linear quantitation range of 100 ng to 1 pg, and our triplex qPCR assay for nDNA/mtDNA/male Y DNA had a linear range of 100 ng to 0.1 ng. Human-specificity was demonstrated by the accurate detection of 0.05% and 5% human DNA, respectively, from a complex source of starting templates. Target-specificity was confirmed by the lack of cross-amplification among targets. A high throughput alternative for human gender determination was also developed by multiplexing the male Y primer/probe set with an X chromosome based system. Background cross-amplification with DNA templates derived from fourteen other species was negligible aside from the male Y assay which produced spurious amplifications from other non-human primate templates. Mainstream application of these assays will undoubtedly benefit forensic genomics.
机译:提供了一整套用于DNA定量的人类特异性,靶特异性,多重PCR分析方法。我们用于nDNA / mtDNA的双链qPCR的线性定量范围为100 ng至1 pg,而用于nDNA / mtDNA /雄性Y DNA的三重qPCR分析的线性范围为100 ng至0.1 ng。通过从复杂的起始模板来源分别准确检测到0.05%和5%的人类DNA证明了人类特异性。靶标之间缺乏交叉扩增,证实了靶标特异性。通过将雄性Y引物/探针组与基于X染色体的系统多路复用,还开发了用于确定性别的高通量替代方案。除了从雄性Y测定法中产生的其他非人灵长类动物模板的假扩增外,与衍生自其他十四个物种的DNA模板的背景交叉扩增可以忽略不计。这些测定的主流应用无疑将有利于法医基因组学。

著录项

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号