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    • 1. 发明授权
    • Cold-active protease CP70
    • 冷活性蛋白酶CP70
    • US06200793B1
    • 2001-03-13
    • US09117245
    • 1998-07-27
    • A. K. M. Quamrul HasanEiichi Tamiya
    • A. K. M. Quamrul HasanEiichi Tamiya
    • C12N952
    • A23J3/341C12N9/52Y10S435/85
    • A psychrophilic protease is here disclosed which has the following physicochemical properties: (a) specific activity and substrate specificity: the protease acts on casein, gelatin, hemoglobin and albumin to specifically decompose them, and the substrate specificity decreases in the order of casein, gelatin, hemoglobin and albumin; (b) optimal pH: 8.0; (c) pH stability: the protease is stable in the range of pH 6.5 to pH 10.0 at 30° C. for 1 hour; (d) optimal temperature: about 40° C.; (e) temperature stability: at pH 7 for 1 hour, the protease is active at a temperature up to 30° C., but it is inactivated at 40° C. as much as about 40% and completely inactivated at 50° C. in about 10 minutes; (f) enzyme activity: the protease has 50% or more of its maximum activity at about 20° C.; (g) the active center of the enzyme is serine; and (h) the molecular weight of the protease is about 70 kDa as measured by SDS-PAGE.
    • 这里公开了一种嗜热蛋白酶,其具有以下物理化学性质:(a)比活性和底物特异性:蛋白酶作用于酪蛋白,明胶,血红蛋白和白蛋白以特异性分解它们,底物特异性按酪蛋白,明胶的顺序降低 ,血红蛋白和白蛋白; (b)最佳pH:8.0; (c)pH稳定性:蛋白酶在30℃下在pH 6.5至pH 10.0范围内稳定1小时; (d)最佳温度:约40℃。 (e)温度稳定性:在pH7下1小时,蛋白酶在高达30℃的温度下是活性的,但在40℃下灭活达40%左右,并在50℃完全失活。 约10分钟; (f)酶活性:蛋白酶在约20℃下具有50%以上的最大活性; (g)酶的活性中心是丝氨酸; 和(h)通过SDS-PAGE测量,蛋白酶的分子量为约70kDa。
    • 3. 发明申请
    • Method for Determination of Test Substance
    • 测定物质的测定方法
    • US20090159458A1
    • 2009-06-25
    • US12226060
    • 2007-03-29
    • Eiichi TamiyaNaoki NagataniTeruko YuhiKagan KermanKoutarou IdegamiMiyuki Chikae
    • Eiichi TamiyaNaoki NagataniTeruko YuhiKagan KermanKoutarou IdegamiMiyuki Chikae
    • G01N27/416G01N33/543
    • G01N33/5438
    • [Problems] A highly sensitive and accurate determination of a test substance is achieved without the need of complicated procedures.[Means for solving the Problems] The presence or absence or the concentration of a test substance 3 can be determined by gathering around the surface of a working electrode 1 metal microparticles 5 in an amount corresponding to the amount of the test substance 3 contained in a test solution, oxidizing the metal microparticles 5 electrochemically, measuring the value of a current produced by electrochemically reducing the oxidized metal, and determining the presence or absence or the concentration of the substance 3 based on the current value. It is preferred that the electrochemical oxidation of the metal microparticles 5 be conducted while maintaining the potential of the working electrode 1 at a value equal to a potential employed for the electrochemical oxidization of the metal microparticles 5.
    • [问题]在不需要复杂程序的情况下实现对测试物质的高度灵敏和准确的测定。 [解决问题的方法]测试物质3的存在或不存在或浓度可以通过将工作电极1的金属微粒5的表面聚集在与金属微粒5中包含的测试物质3的量相当的量 测试溶液,电化学氧化金属微粒5,测量通过电化学还原氧化金属产生的电流的值,并根据当前值确定物质3的存在或不存在或浓度。 优选的是,在将工作电极1的电位保持在与金属微粒5的电化学氧化的电位相等的值的情况下,进行金属微粒5的电化学氧化。
    • 6. 发明授权
    • Analytical method and analytical apparatus
    • 分析方法和分析仪器
    • US08110406B2
    • 2012-02-07
    • US12085466
    • 2006-11-27
    • Eiichi TamiyaNaoki NagataniTeruko YuiTatsurou EndouRyou Tanaka
    • Eiichi TamiyaNaoki NagataniTeruko YuiTatsurou EndouRyou Tanaka
    • G01N33/53
    • G01N33/54393Y10S435/97
    • [PROBLEMS] To reduce the amount of, for example, a capturing antibody to be employed without lowering detection sensitivity. At the same time, to enable the achievement of intense color development or light emission in a determination area even in the case where only a small amount of a labeled antibody is accumulated. To lower the detection limit in the sandwich method. To enlarge the dynamic range in the competition method. [MEANS FOR SOLVING PROBLEMS] A method of analyzing a test substance by an immunological analysis method by using the test substance, a support having a determination area, on which one member selected from a capturing antibody capable of binding specifically to the test substance and a capturing antigen capable of binding specifically to the test substance has been immobilized, and a labeled antibody capable of binding specifically to the test substance, wherein a label having a sensitizing effect has been immobilized on the determination area of the support.
    • [问题]减少例如所用的捕获抗体的量而不降低检测灵敏度。 同时,即使在只有少量的标记抗体被累积的情况下,也可以在确定区域中实现强烈的显色或发光。 降低夹心法的检测限。 在比赛方式中扩大动态范围。 用于解决问题的手段通过使用被检物质的免疫学分析方法分析检测物质的方法,具有测定区域的载体,其中选自能够特异性结合测试物质的捕获抗体中的一个和 已经固定了能够特异性结合测试物质的捕获抗原,并且能够特异性结合测试物质的标记抗体,其中具有敏化作用的标签已被固定在载体的确定区域上。
    • 7. 发明申请
    • Analytical Method and Analytical Apparatus
    • 分析方法和分析仪器
    • US20090047746A1
    • 2009-02-19
    • US12085466
    • 2006-11-27
    • Eiichi TamiyaNaoki NagataniTeruko YuiTatsurou EndouRyou Tanaka
    • Eiichi TamiyaNaoki NagataniTeruko YuiTatsurou EndouRyou Tanaka
    • G01N33/543G01N21/00
    • G01N33/54393Y10S435/97
    • [PROBLEMS] To reduce the amount of, for example, a capturing antibody to be employed without lowering detection sensitivity. At the same time, to enable the achievement of intense color development or light emission in a determination area even in the case where only a small amount of a labeled antibody is accumulated. To lower the detection limit in the sandwich method. To enlarge the dynamic range in the competition method. [MEANS FOR SOLVING PROBLEMS] A method of analyzing a test substance by an immunological analysis method by using the test substance, a support having a determination area, on which one member selected from a capturing antibody capable of binding specifically to the test substance and a capturing antigen capable of binding specifically to the test substance has been immobilized, and a labeled antibody capable of binding specifically to the test substance, wherein a label having a sensitizing effect has been immobilized on the determination area of the support.
    • [问题]减少例如所用的捕获抗体的量而不降低检测灵敏度。 同时,即使在只有少量的标记抗体被累积的情况下,也可以在确定区域中实现强烈的显色或发光。 降低夹心法的检测限。 在比赛方式中扩大动态范围。 用于解决问题的手段通过使用被检物质的免疫学分析方法分析检测物质的方法,具有测定区域的载体,其中选自能够特异性结合测试物质的捕获抗体中的一个和 已经固定了能够特异性结合测试物质的捕获抗原,并且能够特异性结合测试物质的标记抗体,其中具有敏化作用的标签已被固定在载体的确定区域上。
    • 10. 发明授权
    • Plasma generating equipment
    • 等离子发生设备
    • US07875825B2
    • 2011-01-25
    • US10593771
    • 2005-03-25
    • Yuzuru TakamuraAkiko IidukaEiichi Tamiya
    • Yuzuru TakamuraAkiko IidukaEiichi Tamiya
    • B23K9/02G01J3/30
    • G01N21/68G01N21/67G01N21/69
    • A method for generating plasma and a method for elemental analysis, each comprising the steps of providing a narrow portion in a flow channel made of an insulation material, the narrow portion having a cross-sectional area markedly smaller than a cross-sectional area of the flow channel; filling the flow channel and the narrow portion with a conductive liquid, and thereafter applying an electric field to the narrow portion, to conduct the electric field through the narrow portion, thereby generating plasma at the narrow portion. An apparatus for generating plasma, the apparatus for generating plasma comprising a narrow portion in a flow channel made of an insulation material, the narrow portion having a cross-sectional area markedly smaller than a cross-sectional area of the flow channel; and a means of applying an electric field to the narrow portion to conduct the electric field through the narrow portion; and an apparatus for emission spectroscopic analysis comprising the apparatus for generating plasma as defined above.
    • 一种用于产生等离子体的方法和元素分析方法,每个方法包括以下步骤:在由绝缘材料制成的流动通道中提供窄部分,所述窄部分的横截面积明显小于所述绝缘材料的横截面面积 流通道 用导电液体填充流路和狭窄部分,然后向狭窄部分施加电场,使电场通过狭窄部分,从而在狭窄部分产生等离子体。 一种用于产生等离子体的装置,所述用于产生等离子体的装置包括由绝缘材料制成的流动通道中的窄部分,所述窄部分具有明显小于所述流动通道的横截面积的横截面面积; 以及向狭窄部分施加电场以通过所述狭窄部分传导电场的装置; 以及用于发射光谱分析的装置,其包括如上所述产生等离子体的装置。