首页> 外国专利> Diagnostic kit for prenatal detection of trisomy 21, comprises primer pairs specific for amplification of short tandem repeat regions in chromosome 21

Diagnostic kit for prenatal detection of trisomy 21, comprises primer pairs specific for amplification of short tandem repeat regions in chromosome 21

机译:用于21三体性的产前检测的诊断试剂盒,包括特异性扩增21号染色体上短串联重复序列区域的引物对

摘要

Diagnostic kit for detecting trisomy 21 in a human fetus comprises at least two pairs of oligonucleotide primers suitable for amplification, by polymerase chain reaction (PCR), of both strands of a target DNA sequence, i.e. a short tandem repeat region (X) of human chromosome 21. Independent claims are also included for the following: (1) microarray for detecting trisomy 21, especially a DNA chip, comprising an array of many separate fields, at least one of which carries an oligonucleotide able to hybridize to DNA that is part of X; and (2) method for detecting trisomy 21.
机译:用于检测人类胎儿中的21三体性的诊断试剂盒包括至少两对适合通过聚合酶链反应(PCR)扩增目标DNA序列的两条链(即人的短串联重复序列(X))的寡核苷酸引物第21号染色体,也包括以下方面的独立权利要求:(1)用于检测21三体的微阵列,尤其是DNA芯片,其包含许多独立区域的阵列,其中至少一个带有能够与部分DNA杂交的寡核苷酸X个; (2)检测21三体的方法。

著录项

  • 公开/公告号DE10059776A1

    专利类型

  • 公开/公告日2002-07-18

    原文格式PDF

  • 申请/专利权人 ADNAGEN AG;

    申请/专利号DE2000159776

  • 申请日2000-12-01

  • 分类号C12Q1/68;

  • 国家 DE

  • 入库时间 2022-08-22 00:27:17

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