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    • 6. 发明申请
    • Multilayer analysis element
    • 多层分析单元
    • US20050186110A1
    • 2005-08-25
    • US11060777
    • 2005-02-18
    • Kentaro NakamuraKazuya KawasakiToshihisa ItoYoshiki SakainoOsamu Seshimoto
    • Kentaro NakamuraKazuya KawasakiToshihisa ItoYoshiki SakainoOsamu Seshimoto
    • G01N31/22
    • G01N31/22
    • It is an object of the invention to provide a multilayer analysis element with small intra-lot and lot-to-lot differences that has high measurement accuracy and which is small in size. The present invention provides a multilayer analysis element for the analysis of a liquid sample, comprising a water impermeable planar support on one side of which at least one functional layer and at least one porous liquid sample spreading layer of non-fibrous porous film are integrally laminated in the mentioned order, wherein said spreading layer comprises a non-fibrous porous film such that, when a liquid sample containing a target substance to be measured is caused to become attached to the surface of said liquid sample spreading layer, where said liquid sample is spread and dispersed, 30% or more of said target substance to be measured can be transferred to the at least one functional layer below said liquid sample spreading layer.
    • 本发明的目的是提供一种具有很小的批量间和批间差异的多层分析元件,其具有高的测量精度并且尺寸小。 本发明提供了一种用于分析液体样品的多层分析元件,其包括不透水平面支撑体,其一侧上至少一个功能层和至少一个非纤维多孔膜的多孔液体样品铺展层整体层压 其中所述扩散层包括非纤维多孔膜,使得当将含有待测物体的液体样品附着在所述液体样品扩散层的表面上时,其中所述液体样品为 扩散和分散,所述待测量的所述目标物质的30%以上可以转移到所述液体样品扩散层下方的至少一个功能层。
    • 7. 发明申请
    • Multilayer analysis element
    • 多层分析单元
    • US20050186109A1
    • 2005-08-25
    • US11060775
    • 2005-02-18
    • Kentaro NakamuraKazuya KawasakiYoshiki SakainoToshihisa ItoOsamu Seshimoto
    • Kentaro NakamuraKazuya KawasakiYoshiki SakainoToshihisa ItoOsamu Seshimoto
    • G01N31/22
    • G01N31/22
    • An object of the invention to provide a multilayer analysis element with small intra-lot and lot-to-lot differences that has high measurement accuracy and which is small in size. The present invention provides a multilayer analysis element for the analysis of a liquid sample, comprising a water impermeable planar support on one side of which at least one functional layer and at least one porous liquid sample spreading layer of non-fibrous porous film are integrally laminated in the mentioned order, wherein the arithmetic mean deviation of the profile (Ra) of a contact surface of the at least one functional layer that is in contact with said porous liquid sample spreading layer of said non-fibrous porous film is 1 μm or less and/or the ten-point height of irregularities (Rz) of said contact surface is 8 μm or less.
    • 本发明的目的是提供一种具有很高的测量精度并且尺寸小的多批次间差异小的多层分析元件。 本发明提供了一种用于分析液体样品的多层分析元件,其包括不透水平面支撑体,其一侧上至少一个功能层和至少一个非纤维多孔膜的多孔液体样品铺展层整体层压 其中与所述非纤维多孔膜的所述多孔液体样品扩散层接触的所述至少一个功能层的接触表面的轮廓(Ra)的算术平均偏差为1μm以下 和/或所述接触表面的十点高度的不规则(Rz)为8μm或更小。
    • 9. 发明授权
    • Homogenous enzyme immunoassay process
    • 均质酶免疫测定法
    • US06287785B1
    • 2001-09-11
    • US09488371
    • 2000-01-20
    • Hiroshi ShinokiOsamu Seshimoto
    • Hiroshi ShinokiOsamu Seshimoto
    • G01N33533
    • G01N33/535G01N33/542G01N33/54306Y10S435/963Y10S435/964Y10S435/969Y10S435/972Y10S436/823Y10S530/866
    • An improved homogeneous enzyme immunoassay process for quantitatively analyzing an antigen by determining the change in the enzymatic activity caused by a reaction between the antigen and an enzyme-labeled antibody. The antigen is reacted with an enzyme-labeled antibody, followed by the reaction with a second antibody capable of recognizing and binding to a different epitope and then with a third antibody capable of recognizing and binding to the second antibody. The enzymatic activity of the labeling enzyme is determined by a water-insoluble substrate. Using the water-insoluble substrate, steric hindrance is enhanced. A highly-sensitive analysis can be carried out by a simple operation even when the antigen has a molecular weight falling within an intermediate range, for example, a range of M.W. 10,000 to 70,000.
    • 一种改进的均匀酶免疫测定方法,用于通过测定由抗原和酶标记的抗体之间的反应引起的酶活性的变化来定量分析抗原。 使抗原与酶标记的抗体反应,然后与能够识别和结合不同表位的第二抗体反应,然后与能够识别和结合第二抗体的第三抗体反应。 标记酶的酶活性由水不溶性底物决定。 使用水不溶性底物,空间位阻增强。 即使当抗原具有分子量落在中间范围内时,也可以通过简单的操作进行高灵敏度分析,例如,10,000至70000MW的范围。