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    • 1. 发明申请
    • ASSAYS
    • WO2009112594A3
    • 2010-03-04
    • PCT/EP2009053106
    • 2009-03-16
    • CLONDIAG GMBHERMANTRAUT EUGENKAISER THOMASTUCHSCHEERER JENSBEIER VICOSCHULZ TORSTENWOESTEMEYER ANKE
    • ERMANTRAUT EUGENKAISER THOMASTUCHSCHEERER JENSBEIER VICOSCHULZ TORSTENWOESTEMEYER ANKE
    • B01L3/00
    • G01N33/58B01L3/50273B01L2200/025B01L2200/0684B01L2300/0816B01L2300/0887B01L2300/123B01L2400/0481Y10T436/25
    • A method for assaying a sample for each of multiple analytes is described. The method includes contacting an array of spaced-apart test zones with a liquid sample (e.g., whole blood). The test zones disposed within a channel of a microfluidic device. The channel is defined by at least one flexible wall and a second wall which may or may not be flexible. Each test zone comprising a probe compound specific for a respective target analyte. The microfluidic device is compressed to reduce the thickness of the channel, which is the distance between the inner surfaces of the walls within the channel. The presence of each analyte is determined by optically detecting an interaction at each of multiple test zones for which the distance between the inner surfaces at the corresponding location is reduced. The interaction at each test zone is indicative of the presence in the sample of a target analyte. Capillary structures of the devices or used in the methods may comprise a matrix and the devices may comprise control elements and methods for assaying of sample may use corresponding controlling activities.
    • 描述了用于分析多种分析物中的每一种的样品的方法。 该方法包括使间隔开的测试区域的阵列与液体样品(例如全血)接触。 测试区域设置在微流体装置的通道内。 通道由至少一个柔性壁和可以是柔性的第二壁限定。 每个测试区域包含对各个目标分析物特异的探针化合物。 微流体装置被压缩以减小通道的厚度,其是通道内的壁的内表面之间的距离。 每个分析物的存在通过光学检测在相应位置处的内表面之间的距离减小的多个测试区域中的每一个处的相互作用来确定。 每个测试区域的相互作用表明样品中目标分析物的存在。 装置的毛细结构或方法中使用的毛细管结构可以包括基质,并且装置可以包括控制元件和用于测定样品的方法可以使用相应的控制活动。
    • 8. 发明申请
    • DEVICE FOR THE MULTIPLICATION AND DETECTION OF NUCLEIC ACIDS
    • 装置用于生殖和对于核酸的检测
    • WO2004087951A2
    • 2004-10-14
    • PCT/EP2004003532
    • 2004-04-02
    • CLONDIAG CHIP TECH GMBHBICKEL RALFELLINGER THOMASERMANTRAUT EUGENKAISER THOMASSCHULZ TORSTENULLRICH THOMAS
    • BICKEL RALFELLINGER THOMASERMANTRAUT EUGENKAISER THOMASSCHULZ TORSTENULLRICH THOMAS
    • B01L3/00B01L7/00G01N21/47G01N21/59C12Q1/68
    • B01L7/52B01L3/5027B01L2200/147B01L2300/0636B01L2300/0654B01L2300/0877G01N21/4738G01N21/59
    • The invention relates to a device for the multiplication and detection of nucleic acids, comprising a temperature controller and/or regulation unit, a reaction chamber, containing a substrate with a detection surface on which a substance library is immobilised and an optical system, by means of which the temporal process of formation of deposit on the detection surface may be detected. The temperature in the reaction chamber may be controlled and/or regulated by means of the temperature controller and/or regulation unit. The invention further relates to a method for the amplification and qualitative and quantitative detection of nucleic acids in a sample, comprising the following steps: a) introduction of the sample into a reaction chamber, formed by a capillary gap between a chamber support and a microarray, whereby the microarray comprises a substrate with nucleic acid probes arranged on array elements thereon, b) amplification of the nucleic acid for detection in the reaction chamber, by means of a cyclical amplification reaction, c) detection of a hybridisation between the nucleic acid for detection and the nucleic acid probes immobilised on the substrate without removal from the reaction chamber of molecules which are not hybridized with the nucleic acids immobilised on the substrate.
    • 本发明涉及一种用于再现的装置和用于检测的核酸,包括温度控制和/或调节单元; 包含具有检测表面在其上的物质库是一个irrmobilisiert载体,其中在所述反应室中的温度通过温度控制和调节单元和/或调节控制的反应室; 和光学系统与沉淀的时间进程是在检测区域中检测到。 本发明还涉及一种用于扩增和核酸的定性和定量检测样品中,包括以下步骤的方法:(a)将所述样品引入反应室中,这是由腔室支撑件和微阵列,其特征在于之间的毛细间隙形成 所述微阵列包含用irrmobilisierten上的核酸探针阵列元件的衬底; (B)通过循环扩增反应的扩增方法在反应室中的核酸; (C)检测irrmobilisierten而不分子在基板上的核酸和核酸探针之间的杂交,从该反应室,与所述核酸在基板上irrmobilisierten未杂交去除。