首页> 外国专利> Determining genetic predisposition to disease, e.g. rheumatoid polyarthritis, by reacting amplicons of polymorphic human leukocyte antigen (HLA) region with both high and low resolution probes

Determining genetic predisposition to disease, e.g. rheumatoid polyarthritis, by reacting amplicons of polymorphic human leukocyte antigen (HLA) region with both high and low resolution probes

机译:确定疾病的遗传易感性,例如类风湿性多关节炎,通过多态性人类白细胞抗原(HLA)区域的扩增子与高分辨率探针和低分辨率探针反应

摘要

Analyzing the genetic predisposition of a subject to diseases comprising treating a liquid sample containing - 1 type of amplicon from - 1 polymorphic region associated with the disease, with - 1 type-specific probe (P1, low resolution) and - 1 subtype-specific probe (P2, high resolution), is new. Analyzing the genetic predisposition of a subject to diseases comprising treating a liquid sample containing - 1 type of amplicon from - 1 polymorphic region associated with the disease, with - 1 type-specific probe (P1, low resolution) and - 1 subtype-specific probe (P2, high resolution), is new. P1 hybridizes to the polymorphic region of - 1 gene, or group of alleles, present on the amplicon while P2 hybridizes to the allele, or group of alleles, specifically recognized by P1. P2 can discriminate between alleles associated with susceptibility and/or resistance to the disease, according to whether they hybridize or not.
机译:分析对象的疾病遗传易感性,包括使用-1型特异性探针(P1,低分辨率)和-1处理包含来自与疾病相关的 -1多态性区域的 -1类型扩增子的液体样品亚型特异性探针(P2,高分辨率)是新的。分析对象的疾病遗传易感性,包括使用-1型特异性探针(P1,低分辨率)和-1处理包含来自与疾病相关的 -1多态性区域的 -1类型扩增子的液体样品亚型特异性探针(P2,高分辨率)是新的。 P1与扩增子上存在的-1基因或等位基因组的多态性区域杂交,而P2与P1特异性识别的等位基因或等位基因组杂交。 P2可以根据是否杂交来区分与疾病易感性和/或抗性相关的等位基因。

著录项

  • 公开/公告号FR2793808A1

    专利类型

  • 公开/公告日2000-11-24

    原文格式PDF

  • 申请/专利权人 BIOMERIEUX;

    申请/专利号FR19990006599

  • 发明设计人 MOUGIN BRUNO;TIERCY JEAN MARIE;

    申请日1999-05-20

  • 分类号C12Q1/68;

  • 国家 FR

  • 入库时间 2022-08-22 01:07:58

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