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Microarray and kit for diagnosing GCPS syndrome

机译:用于诊断GCPS综合征的微阵列和试剂盒

摘要

PURPOSE: A microarray and a kit for diagnosing GCPS(Greig cephalopolysyndactyly) syndrome are provided to dye a sample with a normal gene copy number and a sample which is suspected to have GCPS syndrome with different fluorescent substances. CONSTITUTION: A microarray and a kit for diagnosing GCPS syndrome contains one or more kinds of genome DNA fragments, 20-100 bp oligonucleotide, 100bp-10kbp cDNA, and one or more kinds of probes. The oligonucleotide is continuously contained in the genome fragment. The cDNA is derived from the genome DNA fragment. The probe is selected from a group consisting of a complement of the genome DNA fragment, oligonucleotide, and cDNA.
机译:目的:提供了一种用于诊断GCPS(格氏多头综合征)综合征的微阵列和试剂盒,以将具有正常基因拷贝数的样品和怀疑具有不同荧光物质的GCPS综合征样品染色。构成:用于诊断GCPS综合征的微阵列和试剂盒包含一种或多种基因组DNA片段,20-100 bp的寡核苷酸,100bp-10kbp cDNA以及一种或多种探针。寡核苷酸连续地包含在基因组片段中。 cDNA源自基因组DNA片段。该探针选自基因组DNA片段,寡核苷酸和cDNA的互补物。

著录项

  • 公开/公告号KR101280816B1

    专利类型

  • 公开/公告日2013-07-02

    原文格式PDF

  • 申请/专利权人

    申请/专利号KR20110087385

  • 申请日2011-08-30

  • 分类号C12N15/11;C12Q1/68;G01N33/58;G01N33/53;

  • 国家 KR

  • 入库时间 2022-08-21 16:24:57

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