首页> 外文OA文献 >Genotyping single nucleotide polymorphisms directly from genomic DNA by invasive cleavage reaction on microspheres
【2h】

Genotyping single nucleotide polymorphisms directly from genomic DNA by invasive cleavage reaction on microspheres

机译:通过微球上的侵入性裂解反应直接从基因组DNA中对单核苷酸多态性进行基因分型

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Here we report proof-of-principle for a microsphere-based genotyping assay that detects single nucleotide polymorphisms (SNPs) directly from human genomic DNA samples. This assay is based on a structure-specific cleavage reaction that achieves single base discrimination with a 5′-nuclease which recognizes a tripartite substrate formed upon hybridization of target DNA with probe and upstream oligonucleotides. The assay is simple with two easy steps: a cleavage reaction, which generates fluorescent signal on microsphere surfaces, followed by flow cytometry analysis of the microspheres. Genomic DNA samples were genotyped for the SNP in the Apolipoprotein E gene at amino acid position 158. The assay successfully scored wild type, heterozygous and homozygous mutants. To our knowledge, this is the first report of a solid-support assay for detection of SNPs directly from genomic DNA without PCR amplification of the target.
机译:在这里,我们报告基于微球的基因分型检测的原理证明,该检测直接从人类基因组DNA样本中检测单核苷酸多态性(SNP)。该测定基于结构特异性切割反应,该反应通过5'核酸酶实现单碱基区分,该5'核酸酶识别在靶DNA与探针和上游寡核苷酸杂交后形成的三重底物。该测定很简单,只需两个简单步骤:裂解反应,该反应在微球表面产生荧光信号,然后对微球进行流式细胞仪分析。对载脂蛋白E基因第158位氨基酸的SNP基因组DNA样本进行了基因分型。该测定成功地对野生型,杂合和纯合突变体进行了评分。据我们所知,这是直接从基因组DNA直接检测SNP而无需PCR扩增靶标的固相支持测定法的首次报道。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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