首页> 外国专利> A METHOD FOR PREPARING THE PRIMERS FOR IN VITRO IDENTIFYING MUTATIONS WITHIN LARGED VESTIBULAR AQUEDUCT SYNDROMIC HEARING LOSS PDS GENE AND THE USE THEREOF

A METHOD FOR PREPARING THE PRIMERS FOR IN VITRO IDENTIFYING MUTATIONS WITHIN LARGED VESTIBULAR AQUEDUCT SYNDROMIC HEARING LOSS PDS GENE AND THE USE THEREOF

机译:一种制备用于在较大的前庭水肿综合征听力丧失PDS基因中体外鉴定突变的方法及其用途

摘要

A method for preparing the primers which can be used to in vitro identify mutations within larged vestibular aqueduct syndromic hearing loss PDS gene. The method comprises designing the primer pairs which can insert any substitution base at the region consisting of 1 to 13 bases which comprising the site IVS7-2A?G and part of the upstream and downstream regions thereof, according to the mutation site IVS7-2A?G within PDS gene, and then obtaining new restriction endonuclease site from the amplified product which can be used to identify IVS7-2 wild type A site and the mutant G. The primers produced by the above method, kit, agent or the like, which comprising the primers, and the method for identifying the mutation which comprising the larged vestibular aqueduct syndrome IVS7-2A?G are also provided.
机译:一种制备引物的方法,该引物可用于体外鉴定大前庭输水管道综合征性听力损失PDS基因内的突变。该方法包括根据突变位点IVS7-2Aβ设计引物对,该引物对可在由1至13个碱基组成的区域插入任何取代碱基,该区域包括IVS7-2AβG位点及其部分上游和下游区域。 PDS基因中的G,然后从扩增产物中获得新的限制性核酸内切酶位点,可用于鉴定IVS7-2野生型A位点和突变体G。通过上述方法,试剂盒,试剂等制备的引物还提供了包含引物的载体,以及鉴定包含大前庭水管综合征IVS7-2AΔG的突变的方法。

著录项

  • 公开/公告号WO2007098671A8

    专利类型

  • 公开/公告日2009-07-02

    原文格式PDF

  • 申请/专利权人 JIN ZHENGCE;DAI PU;HAN DONGYI;

    申请/专利号WO2007CN00260

  • 发明设计人

    申请日2007-01-24

  • 分类号C12Q1/68;C07K14/435;C12N15/12;

  • 国家 WO

  • 入库时间 2022-08-21 19:21:57

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