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    • 61. 发明申请
    • APPARATUS AND METHOD FOR MEASURING 8-OHdG
    • 用于测量8-OHdG的装置和方法
    • US20070077662A1
    • 2007-04-05
    • US11470955
    • 2006-09-07
    • Yohei InabaKenji YokoyamaIsao KarubeNarushi Ito
    • Yohei InabaKenji YokoyamaIsao KarubeNarushi Ito
    • G01N1/18
    • G01N30/88G01N2030/8813Y10T436/255
    • To provide a method for effectively and simply separating and condensing 8-OHdG which is present by a trace amount in body fluid, particularly in urine, and is frequently mingled with foreign substances with their peaks appearing around the peak thereof, a simple measurement method of 8-OHdG, and an apparatus for the measurement. [Solution]The present invention provides a method for effectively and simply separating and condensing 8-OHdG by an optimum combination of chromatographies. Specifically, the present invention comprises a method for separating and condensing 8-hydroxy-2′-deoxyguanosine (8-OHdG) from a body fluid, wherein a urine sample is contacted with a hydrophobic adsorbent which has, as the functional group, a straight chain hydrocarbon group having a carbon number of 6-30 and has a C % of 18% or less to capture the 8-OHdG. The method for measuring 8-OHdG and the apparatus for the measurement method according to the present invention use electrochemical reaction to measure the amount of 8-OHdG in the sample.
    • <待解决的问题>提供一种有效且简单地分离和冷凝8-OHdG的方法,其通过微量的体液,特别是尿中存在,并且经常与外来物质混合,其峰出现在其峰顶周围 ,8-OHdG的简单测量方法和用于测量的装置。 [解决方案]本发明提供了通过色谱的最佳组合有效且简单地分离和冷凝8-OHdG的方法。 具体地说,本发明包括从体液中分离和浓缩8-羟基-2'-脱氧鸟苷(8-OHdG)的方法,其中使尿样与疏水性吸附剂接触,所述疏水性吸附剂具有作为官能团的直链 碳原子数为6〜30的碳原子数为8〜8的C-C的烃基,捕捉8-OHdG。 根据本发明的用于测量8-OHdG的方法和测量方法的装置使用电化学反应来测量样品中8-OHdG的量。
    • 62. 发明申请
    • Method for measuring substance having affinity
    • 测量具有亲和性的物质的方法
    • US20070000311A1
    • 2007-01-04
    • US10561105
    • 2004-06-11
    • Isao KarubeKeisuke Iwata
    • Isao KarubeKeisuke Iwata
    • G01N30/00
    • G01N15/12G01N15/04G01N33/561
    • The binding reaction between an affinity substance to be measured and a binding partner having binding affinity for the affinity substance is measured based on agglutination reactions. Carrier particles bound to the binding partner are allowed to bind to the affinity substance in an electric field. Evaluation is achieved by counting the level of agglutinated carrier particles using three-dimensional particle information of the particles as an indicator. The use of three-dimensional information as an indicator enables the presence of a biologically specific reactive substance to be detected or measured in a manner that is more convenient and rapid, and has a higher sensitivity than the conventional measurement methods.
    • 基于凝集反应测定待测亲和性物质与亲和物质结合亲和力的结合对象之间的结合反应。 与结合配偶体结合的载体颗粒在电场中与亲和物质结合。 通过使用颗粒的三维粒子信息作为指标计数凝集载体颗粒的水平来实现评估。 使用三维信息作为指标,可以以更方便快捷的方式检测或测量生物特异性反应物质的存在,并且具有比常规测量方法更高的灵敏度。
    • 67. 发明授权
    • Site-specific cell perforation technique
    • 位点特异性细胞穿孔技术
    • US06753171B2
    • 2004-06-22
    • US09623970
    • 2000-12-28
    • Isao KarubeTakashi Saitoh
    • Isao KarubeTakashi Saitoh
    • C12N1509
    • C12N15/89C12M35/00C12N13/00
    • A technique for controlling membrane denaturation reactions other than physical shear force was developed. For example, the present invention provides, a method for causing membrane disruption at a specific site by reacting a stimulus such as light with a compound that is activated by the stimulus, where the reaction occurs on a membrane such as a biomembrane. It also provides a membrane structure such as cells in which a specific site has been disrupted, which are obtained by the present method. Introduction of substances such as genes also became possible by using this membrane structure. Further provided is a membrane-destroying member for disrupting a membrane at a specific site. Thus, the present invention enabled, for example, easy membrane penetration using components constituting microelectrodes, micromanipulators, and microinjectors, which were conventionally hardly usable in penetrating cell membranes.
    • 开发了除物理剪切力之外控制膜变性反应的技术。 例如,本发明提供了通过使诸如光的刺激与由刺激激活的化合物反应而使特定部位的膜破裂的方法,其中反应发生在诸如生物膜的膜上。 还提供了通过本方法获得的膜结构,例如其中特异性位点已被破坏的细胞。 使用这种膜结构也可以引入基因等物质。 还提供了用于破坏特定部位的膜的破坏薄膜的部件。 因此,本发明能够例如使用通常难以用于穿透细胞膜的微电极,显微操纵器和显微注射器的构成的薄膜穿透。
    • 69. 发明授权
    • Method for determining biochemical oxygen demand
    • 确定生化需氧量的方法
    • US4350763A
    • 1982-09-21
    • US138121
    • 1980-04-07
    • Shuichi SuzukiIsao Karube
    • Shuichi SuzukiIsao Karube
    • G01N33/18
    • G01N33/1806Y10S435/817
    • The biochemical oxygen demand (BOD) of an aqueous liquid contaminated with organic matter is determined by contacting a sample solution with elementary oxygen and with immobilized microorganisms capable of aerobically metabolizing the organic matter and of thereby consuming the oxygen. The rate of oxygen consumption under otherwise uniform conditions is as precise a measure of BOD as the conventional five-day test, but is determined within less than two hours, usually less than 30 minutes. A membrane-type oxygen-sensitive electrode is employed for sensing the rate of oxygen consumption and generates an output signal which is readily correlated with the BOD of the tested liquid.
    • 用有机物质污染的含水液体的生物化学需氧量(BOD)是通过使样品溶液与基本氧接触的固体微生物和能够有机代谢有机物质并从而消耗氧气的固定化微生物来确定的。 在其他均匀条件下的氧消耗速率与常规五天试验一样精确地测量BOD,但是在不到两小时,通常少于30分钟内测定。 使用膜式氧敏电极来感测氧消耗的速率,并产生容易与被测液体的BOD相关的输出信号。