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MICROARRAY AND KIT FOR DIAGNOSING LANGER-GIEDION SYNDROME

机译:微阵列和工具箱诊断血管扩张综合征

摘要

PURPOSE: A microarray and a kit for diagnosing Langer-Giedion syndrome are provided to identify an accurate amplification of a gene by dyeing two samples with different fluorescent substances and expressing the ratio value of the dyeing difference between the two samples numerically, thereby shortening the diagnosis time. CONSTITUTION: A microarray for diagnosing Langer-Giedion syndrome contains genome DNA fragments of one or more kinds, 20-100bp oligonucleotide, 100bp-10kbp cDNA, and probes of one or more kinds. The 20-100bp oligonucleotide is subsequently arranged inside the genome DNA fragments. The cDNA is derived from the genome DNA fragments. The probes are selected from a group consisting of the complements of the genome DNA fragments, oligonucleotide, and cDNA. For the probes, the maximum rate of containing repetitive sequence in the base sequence is 85%. The base sequence comprising the probes has a feature of single locus in chromosomes.
机译:目的:提供一种用于诊断Langer-Giedion综合征的微阵列和试剂盒,以通过将两个样品用不同的荧光物质染色并数字表达两个样品之间的染色差异的比率值来鉴定基因的准确扩增,从而缩短诊断时间时间。构成:用于诊断Langer-Giedion综合征的微阵列包含一种或多种基因组DNA片段,20-100bp的寡核苷酸,100bp-10kbp cDNA以及一种或多种探针。随后将20-100bp的寡核苷酸排列在基因组DNA片段内。 cDNA源自基因组DNA片段。探针选自基因组DNA片段,寡核苷酸和cDNA的互补物。对于探针,在碱基序列中包含重复序列的最大比率为85%。包含探针的碱基序列在染色体中具有单一基因座的特征。

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