首页> 外国专利> A NEW FLUORESCENT BEACON PROBE DIAGNOSTIC TOOL/KIT FOR MILECULAR DETECTION OF TRANSLOCATION T(9;22)/BCR-ABL1 IN LEUKEMIC PATIENTS AND METHOD OF WORKING FOR THE SAME

A NEW FLUORESCENT BEACON PROBE DIAGNOSTIC TOOL/KIT FOR MILECULAR DETECTION OF TRANSLOCATION T(9;22)/BCR-ABL1 IN LEUKEMIC PATIENTS AND METHOD OF WORKING FOR THE SAME

机译:用于白血病患者分子易位T(9; 22)/ BCR-ABL1分子检测的新型荧光信标探针诊断工具/套件及其工作方法

摘要

The present invention provides method for detecting chromosomal abnormalities in leukemic patients and particularly uses nucleic acid hybridization technique for detection of BCR-ABLl translocation/ t(9;22)(q34;qll) or the so called Philadelphia chromosome which is found in 95% of Chronic Myeloid Leukemia ,15-20% acute lymphoid leukemia and 5% of Acute Myeloid Leukemia patients . The invention focuses on an easy, inexpensive/pocket friendly, rapid and efficient detection of commonly found b2a2 transcript (RNA) of BCR-ABLl from peripheral venous blood of leukemia patients by using beacon based oligonucleotide fluorescent probe which detects the transcribed regions on both sides of the junction formed in the fusion gene upon translocation.
机译:本发明提供了用于检测白血病患者的染色体异常的方法,并且特别是使用核酸杂交技术来检测BCR-ABL1易位/ t(9; 22)(q34; qll)或所谓的费城染色体,其发现率为95%。慢性粒细胞白血病的发生率,15-20%的急性淋巴性白血病和5%的急性髓性白血病患者。本发明集中于通过使用基于信标的寡核苷酸荧光探针来检测白血病患者外周静脉血中BCR-ABL1的常见b2a2转录本(RNA),该信标基于寡核苷酸荧光探针,该探针可检测两侧的转录区域,从而容易,廉价/友好易位时在融合基因中形成的连接点的示意图。

著录项

  • 公开/公告号IN2013DE01569A

    专利类型

  • 公开/公告日2013-11-08

    原文格式PDF

  • 申请/专利权人

    申请/专利号IN1569/DEL/2013

  • 申请日2013-05-24

  • 分类号

  • 国家 IN

  • 入库时间 2022-08-21 16:41:00

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