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    • 83. 发明申请
    • 2-IN-1 BIOCHIP
    • US20100147688A1
    • 2010-06-17
    • US12161114
    • 2006-01-19
    • Mohamed Roshdy Soliman El Hadidy
    • Mohamed Roshdy Soliman El Hadidy
    • G01N27/00B01D57/02
    • B01L3/502753B01L3/502715B01L2200/027B01L2200/0631B01L2200/10B01L2300/0645G01N27/4473G01N27/44791G01N33/492
    • This invention relates to the Capillary Electrophoresis (CE) Biochip. This chip uses the technology of CE combined with conductivity detection to determine: blood Electrolytes (EL) of K3 Na, Ca & Li using “EL Biochip” and to monitor water quality using “L Biochip”. Our in use technology enables to develop a small chip, reliable, easy to use, inexpensive and capable for rapid whole blood testing anywhere. Once this technique is developed, a generic system is obtained, and multitude of ions can be tested at once on the same device. Our chips are using same hardware (layout) and can be optimized to test other ions. The “2-in-1 Biochip” is a multi application versatile system, having two chips : “EL Biochip” : a point-of-care blood analysis chip, for diagnosis & therapeutic follow-up. “L-Biochip”: an on-site environmental monitoring liquids chip, to monitor water quality & guarding against water born diseases outbreaks.
    • 本发明涉及毛细管电泳(CE)生物芯片。 该芯片采用CE与电导率检测技术结合使用“EL Biochip”测定K3 Na,Ca&Li的血液电解质(EL),并使用“L Biochip”监测水质。 我们的使用技术可以开发出小巧的芯片,可靠,易于使用,价格低廉,能够在任何地方快速全血测试。 一旦开发了这种技术,就可以获得一个通用的系统,并且可以在同一个设备上同时测试大量的离子。 我们的芯片使用相同的硬件(布局),可以进行优化,以测试其他离子。 “2合1生物芯片”是一种多应用多功能系统,具有两个芯片:“EL Biochip”:一种点对点血液分析芯片,用于诊断和治疗后续。 “生物芯片”:现场环境监测液体芯片,监测水质,防范出生水肿疾病爆发。
    • 85. 发明申请
    • GRADIENT ELUTION ELECTROPHORESIS AND DETECTORLESS ELECTROPHORESIS APPARATUS
    • 梯度电解电泳和无电极电泳设备
    • US20100089757A1
    • 2010-04-15
    • US12577494
    • 2009-10-12
    • David J. RossSam ForryJason Kralj
    • David J. RossSam ForryJason Kralj
    • B01D57/02G01N27/26
    • G01N27/44713B01D57/02G01N27/4473G01N2030/285
    • A microfluidic apparatus and method for performing electrophoretic separation of compounds. The apparatus comprises: a) A first container for containing a sample fluid; b) a second container for containing a separation buffer fluid; c) a channel of a first length having an inlet end and an outlet end, the inlet end connected to the first container and the outlet end connected to the second container; d) a voltage device electrically connected to the first container and the second container, the voltage device facilitating adjustment of the amount of voltage to the first container and the second container; e) a controller for controlling the velocity flow of the sample fluid through the channel from the first container towards the second container; and f) a measuring device for measuring the current through the channel. The method comprises the steps of: a) providing a separation buffer; b) providing a sample solution in fluid contact with the separation buffer; c) applying an electric field to the separation buffer; and d) producing a variable bulk flow of the separation buffer in a direction substantially aligned with said electric field. Fluid contact between the separation buffer and the sample solution is made through a separation column having a length in the range of from approximately 0.01 mm to approximately 5 mm. By the foregoing, compounds can be sequentially detected and quantified.
    • 用于进行化合物电泳分离的微流体装置和方法。 该装置包括:a)容纳样品流体的第一容器; b)用于容纳分离缓冲液的第二容器; c)具有入口端和出口端的第一长度的通道,入口端连接到第一容器,出口端连接到第二容器; d)与第一容器和第二容器电连接的电压装置,该电压装置有助于调节第一容器和第二容器的电压量; e)控制器,用于控制样品流体通过通道从第一容器朝向第​​二容器的速度流动; 以及f)用于测量通过通道的电流的测量装置。 该方法包括以下步骤:a)提供分离缓冲液; b)提供与分离缓冲液流体接触的样品溶液; c)向分离缓冲器施加电场; 以及d)在与所述电场基本对齐的方向上产生分离缓冲液的可变体积流。 分离缓冲液和样品溶液之间的流体接触通过长度在约0.01mm至约5mm范围内的分离柱制成。 通过上述,可以顺序地检测和定量化合物。
    • 86. 发明申请
    • Monitored separation device
    • 监测分离装置
    • US20100035228A1
    • 2010-02-11
    • US11091605
    • 2005-03-28
    • George William JacksonRichard Coale WillsonGeorge Edward Fox
    • George William JacksonRichard Coale WillsonGeorge Edward Fox
    • C12Q1/70G01N27/26B01D57/02G01N33/53
    • C12N15/1003B01D57/02G01N27/44721
    • A device for separating and purifying useful quantities of particles comprises: a. an anolyte reservoir connected to an anode, the anolyte reservoir containing an electrophoresis buffer; b. a catholyte reservoir connected to a cathode, the catholyte reservoir also containing the electrophoresis buffer; c. a power supply connected to the anode and to the cathode; d. a column having a first end inserted into the anolyte reservoir, a second end inserted into the catholyte reservoir, and containing a separation medium; e. a light source; f. a first optical fiber having a first fiber end inserted into the separation medium, and having a second fiber end connected to the light source; g. a photo detector; h. a second optical fiber having a third fiber end inserted into the separation medium, and having a fourth fiber end connected to the photo detector; and i. an ion-exchange membrane in the anolyte reservoir.
    • 用于分离和净化有用量的颗粒的装置包括:a。 连接到阳极的阳极电解液储存器,含有电泳缓冲液的阳极电解液储存器; b。 连接阴极的阴极电解液储存器,阴极电解液储存器还含有电泳缓冲液; C。 连接到阳极和阴极的电源; d。 柱,其具有插入所述阳极电解液容器的第一端,插入所述阴极电解液容器中的第二端,并且包含分离介质; e。 光源; F。 第一光纤,其具有插入到所述分离介质中的第一光纤端,并且具有连接到所述光源的第二光纤端; G。 光电检测器 H。 第二光纤,其具有插入到所述分离介质中的第三光纤端,并且具有连接到所述光检测器的第四光纤端; 和我。 阳极电解液容器中的离子交换膜。
    • 88. 发明授权
    • Method for analyzing nucleic acid and use thereof for evaluating the degree of mRNA editing of the serotonin 5-HT2C receptor
    • 核酸分析方法及其用于评价血清素5-HT 2C受体的mRNA编辑程度的方法
    • US07635558B2
    • 2009-12-22
    • US10522592
    • 2003-07-24
    • Jean-Jacques MadjarHervé Berthomme
    • Jean-Jacques MadjarHervé Berthomme
    • C12Q1/68C12P19/34C07H21/02C07H21/04C07H21/00B01D57/02
    • C12Q1/6827C12Q1/6813C12Q1/6837C12Q2537/143C12Q2527/107C12Q2525/101C12Q2565/131C12Q2521/107
    • The invention concerns a method for analyzing nucleic acids using a small-size probe array comprising deoxyinostines (dI) instead of deoxyguanogines (dG). The invention also concerns such probe arrays and their use in methods for detecting and/or quantifying target oilgonucleotides present in DNA (deoxyribonucleic acid) or RNA (ribonucleic acid) molecules in a sample, in particular mRNA editing rate of the serotonin 5-HT2C receptor (5-HT2C-R). The invention further concerns a biochip or a reactor in liquid medium comprising such probe arrays as well as their uses, in particular for detecting and/or identifying genetic polymorphisms or for determining an mRNA editing rate, whether it is that of a 5-HT2C-R mRNA or any other RNA capable of being edited. The invention also concerns a method based on the isolation of a single strand conformation polymorphism (SSCP) enabling under specific analysis conditions the editing profile and/or rate of an mRNA capable of being edited to be obtained, as well as a method for diagnosing diseases or susceptibility to diseases associated with the degree of edition of an mRNA. Finally, the invention concerns a method for selecting compounds capable of modulating mRNA editing rate, in particular that of 5-HT2C-R, as well as the use of such compounds for preparing a pharmaceutical composition for treating organic fluid.
    • 本发明涉及使用包含脱氧肌苷(dI)而不是脱氧鸟苷(dG)的小尺寸探针阵列分析核酸的方法。 本发明还涉及这种探针阵列及其在检测和/或定量存在于样品中的DNA(脱氧核糖核酸)或RNA(核糖核酸))分子中的靶油核苷酸的方法中的用途,特别是5-羟色胺5-HT 2C受体的mRNA编辑速率 (5-HT 2C-R)。 本发明还涉及包含这种探针阵列的液体培养基中的生物芯片或反应器,以及它们的用途,特别是用于检测和/或鉴定遗传多态性或用于确定mRNA编辑速率,无论是5-HT 2C- R mRNA或任何其他能够编辑的RNA。 本发明还涉及基于分离单链构象多态性(SSCP)的方法,其能够在特定分析条件下使得能够获得编辑的mRNA的编辑谱和/或速率以及用于诊断疾病的方法 或对与mRNA的编程程度相关的疾病的易感性。 最后,本发明涉及一种选择能够调节mRNA编辑速率的化合物,特别是5-HT 2C-R的化合物的方法,以及这些化合物在制备用于治疗有机液体的药物组合物中的用途。