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MICROARRAY AND KIT FOR DIAGNOSING 1P36 DELETION SYNDROME

机译:诊断1P36缺失综合征的微阵列和套件

摘要

PURPOSE: A microarray and a kit for diagnosing 1p36 deletion syndrome are provided to dye samples with different fluorescent substances, and to accurately detect gene amplification. CONSTITUTION: A microarray and a kit for diagnosing 1p36 deletion 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 placed in the genome DNA fragment. cDNA is derived from the genome DNA fragment. The probe has 85% or less of repetitive sequences.
机译:目的:提供一种用于诊断1p36缺失综合征的微阵列和试剂盒,以对具有不同荧光物质的样品进行染色,并准确检测基因扩增。组成:一种用于诊断1p36缺失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寡核苷酸,100bp-10kbp cDNA以及一种或多种探针。寡核苷酸连续地置于基因组DNA片段中。 cDNA源自基因组DNA片段。探针具有85%或更少的重复序列。

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