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Mutual reaction action method of detection and bioassay device, and baseplate for bioassay

机译:检测与生物测定装置的相互反应作用方法及生物测定用基板

摘要

In a cell detecting part (2), an end face (13a) of a cantilever (13) is previously surface treated so that a detecting nucleotide chain D can be fixed thereto. In a reaction area (10), an electric field is generated by a cathode (11) and an anode (12). A target nucleotide chain T dripped from a nozzle (3) moves to the end face (13a) while the target nucleotide chain T is stretched. When the detecting nucleotide chain D and the target nucleotide chain T are hybridized, the mass of the cantilever (13) is increased to lower a natural frequency. Thus, ac voltage is applied to the cantilever (13) to measure the change of the natural frequency. Thus, whether or not there is the hybridization is detected and the number of the hybridized target nucleotide chains T is quantitatively detected. IMAGE
机译:在细胞检测部(2)中,预先对悬臂(13)的端面(13a)进行表面处理,从而可以将检测核苷酸链D固定在其上。在反应区域(10)中,由阴极(11)和阳极(12)产生电场。从喷嘴(3)滴下的目标核苷酸链T在延伸的同时向端面(13a)移动。当检测核苷酸链D和目标核苷酸链T杂交时,悬臂(13)的质量增加以降低自然频率。因此,向悬臂(13)施加交流电压以测量固有频率的变化。因此,检测是否存在杂交,并且定量检测杂交的靶核苷酸链T的数目。 <图像>

著录项

  • 公开/公告号JP4329322B2

    专利类型

  • 公开/公告日2009-09-09

    原文格式PDF

  • 申请/专利权人 ソニー株式会社;

    申请/专利号JP20020292861

  • 发明设计人 木下 隆;真峯 隆義;

    申请日2002-10-04

  • 分类号G01N13/10;C12M1/00;C12N15/09;C12Q1/68;G01N37/00;

  • 国家 JP

  • 入库时间 2022-08-21 19:38:58

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