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Systems and methods to quantify and amplify both signaling probes for cDNA chips and genes expression microarrays

机译:定量和扩增cDNA芯片和基因表达微阵列的信号探针的系统和方法

摘要

The invention provides a series of reagent compositions and methods for making and amplifying novel cDNA based probe sets from RNA samples to improve analysis with gene expression arrays. The methods globally produce probe sets with common universal linkers at one or both ends, called WRAP-Probes, wherein the linkers do not bind to the target sequences and they can efficiently bind added reporters to the probes. The universal linkers are also designed as primer binding sites for copying and amplifying the probes, either linearly with one linker, or exponentially with double linkers. The capacity to globally and exponentially amplify the probe set by PCR is a primary advantage. Adding reporters by terminal linkers also improves quantification since each probe gets equivalent signaling. The invention allows expression analysis of small research, clinical and forensic samples to enable improved diagnostics, drug discovery, therapeutic monitoring, and medical, agricultural and general research.
机译:本发明提供了一系列试剂组合物和方法,用于从RNA样品中制备和扩增新的基于cDNA的探针组,以改善基因表达阵列的分析。该方法总体上产生在一端或两端具有通用通用接头的探针组,称为WRAP-Probes,其中接头不与靶序列结合,并且它们可以有效地将添加的报道分子与探针结合。通用接头还被设计为引物结合位点,用于与一个接头线性地或与双接头指数地复制和扩增探针。通过PCR全局和指数扩增探针组的能力是主要优势。通过末端连接子添加报告基因还可以改善定量,因为每个探针都获得了等同的信号传导。本发明允许对小型研究,临床和法医样品进行表达分析,以实现改进的诊断,药物发现,治疗监测以及医学,农业和普通研究。

著录项

  • 公开/公告号US7482443B2

    专利类型

  • 公开/公告日2009-01-27

    原文格式PDF

  • 申请/专利权人 DAVID A. SHAFER;

    申请/专利号US20030380596

  • 发明设计人 DAVID A. SHAFER;

    申请日2001-03-09

  • 分类号C07H21/04;C12Q1/68;C12P19/34;

  • 国家 US

  • 入库时间 2022-08-21 19:29:27

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