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Kit for measuring and measurement method of double-stranded DNA content

机译:用于测定双链DNA含量的试剂盒和测定方法

摘要

Provided are a method for electrochemically determining the amount of double-stranded DNA in a simple manner and with excellent precision, which does not need any expensive measurement electrode such as immobilized enzyme electrode or any high-level electrode production technique which can retain a uniform surface area accuracy; and a kit for a determination using the method. Disclosed are a method for electrochemically determining the amount of double-stranded DNA in a sample solution based on a residual amount of a substance capable of binding to the double-stranded DNA which is added to the solution in excess amount; and a kit for a determination using the method. In the method or the kit, a buffering substance is added to the sample solution. The buffering substance is a substance capable of allowing an oxidation wave potential of the potential-current curve for the substance capable of binding to the double-stranded-DNA determined in a solution containing the buffering substance to change depending upon concentration of the free substance capable of binding to the double-stranded DNA in the solution.
机译:提供了一种以简单的方式并且以优异的精度电化学确定双链DNA的量的方法,其不需要任何昂贵的测量电极例如固定化酶电极或任何可以保持均匀表面的高级电极生产技术。面积精度以及使用该方法进行测定的试剂盒。本发明公开了一种基于剩余量的能够与过量添加到溶液中的双链DNA结合的物质的残留量,电化学测定样品溶液中双链DNA的量的方法。以及使用该方法进行测定的试剂盒。在该方法或试剂盒中,将缓冲物质添加到样品溶液中。缓冲物质是能够使包含缓冲物质的溶液中确定的能够与双链DNA结合的物质的电位-电流曲线的氧化波电位根据能够游离的物质的浓度而变化的物质。与溶液中双链DNA的结合。

著录项

  • 公开/公告号JP5286786B2

    专利类型

  • 公开/公告日2013-09-11

    原文格式PDF

  • 申请/专利权人 三菱瓦斯化学株式会社;

    申请/专利号JP20070549047

  • 发明设计人 坂本 斉;

    申请日2006-11-16

  • 分类号G01N27/416;C12Q1/68;C12N15/09;

  • 国家 JP

  • 入库时间 2022-08-21 16:59:43

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