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    • 1. 发明申请
    • MUCOSA ANALYSIS
    • 粘膜分析
    • WO2017064371A1
    • 2017-04-20
    • PCT/FI2016/050721
    • 2016-10-16
    • AQSENS OY
    • SIIVONEN, JoonasTIITTANEN, Satu
    • G01N33/574
    • G01N33/57407G01N33/52G01N2458/40G01N2800/7028
    • The present invention is related to a method for determining mucosa alterations in a subject, in particular to a method for determining mucosa alterations in a sample using a reagent comprising a lanthanide(III) ion, and an array of indicator molecules configured to interact with the sample. The reagent comprising the lanthanide(III) ion does not have any sample or indicator molecule specific recognition elements. The invention relates also to an array for determining mucosa alterations, the array comprising one or more indicator molecules configured to interact specifically with the sample and a reagent comprising a lanthanide(III) ion. The reagent comprising a lanthanide(III)does not have any sample or indicator molecule specific recognition elements.
    • 本发明涉及用于确定受试者中粘膜改变的方法,具体涉及使用包含镧系元素(III)离子的试剂确定样品中的粘膜改变的方法,以及阵列 的指示剂分子被配置成与样品相互作用。 包含镧系元素(III)离子的试剂不具有任何样品或指示剂分子特异性识别元件。 本发明还涉及用于确定粘膜改变的阵列,所述阵列包含一种或多种指示剂分子,所述指示剂分子被配置成与所述样品特异性相互作用,所述试剂包含镧系元素(III)离子。 包含镧系元素(III)的试剂不具有任何样品或指示剂分子特异性识别元件。
    • 4. 发明申请
    • METHOD FOR DETECTING MEMBRANE PROTEIN INTERNALIZATION
    • 检测膜蛋白内含物的方法
    • WO2010012962A2
    • 2010-02-04
    • PCT/FR2009051538
    • 2009-07-30
    • CIS BIO INTZWIER JURRIAANPOOLE ROBERTANSANAY HERVEFINK MICHELTRINQUET ERIC
    • ZWIER JURRIAANPOOLE ROBERTANSANAY HERVEFINK MICHELTRINQUET ERIC
    • G01N33/566G01N33/58
    • G01N33/542G01N33/5035G01N33/58G01N2458/40Y10T436/13
    • A method for detecting the internalization of a transmembrane protein of interest expressed at the surface of a cell, comprising the following steps: a) labelling the protein of interest with a fluorescent metal complex, the lifetime of which is greater than 0.1 ms; b) adding to the reaction medium a composition capable of causing the internalization of the protein of interest; c) adding to the reaction medium a modulating agent selected from: a. a fluorescent or nonfluorescent FRET acceptor compound compatible with said fluorescent metal complex, the final concentration of which in the reaction medium is greater than 10-7 M; b. a reducing agent, the redox potential of which is less than +0.1 V and preferably between 0.25 and 0.75 V; c. an agent which binds specifically, by noncovalent bonding, with the fluorescent metal complex; d. a metal ion which competes with the rare earth so as to form a nonfluorescent metal complex; d) measuring the luminescence emitted by the reaction medium at the emission wavelength of the fluorescent metal complex and/or at the emission wavelength of the modulating compound when said compound is a fluorescent acceptor compound; e) comparing the signal measured in step d) with a reference signal measured on cells having been subjected only to steps a) and c). Use: Method for detecting membrane protein internalization.
    • 一种用于检测在细胞表面表达的目标跨膜蛋白的内在化的方法,包括以下步骤:a)用荧光金属络合物标记感兴趣的蛋白质,其寿命大于0.1ms; b)向反应介质中加入能够引起目的蛋白质内化的组合物; c)向反应介质中加入选自以下的调节剂:a。 与所述荧光金属络合物相容的荧光或非荧光FRET受体化合物,其最终浓度在反应介质中大于10-7M; 湾 还原剂,其氧化还原电位小于+0.1V,优选0.25至0.75V; C。 通过非共价键合与荧光金属络合物特异性结合的试剂; 天。 与稀土竞争以形成非荧光金属络合物的金属离子; d)当所述化合物是荧光受体化合物时,测量在荧光金属络合物的发射波长处和/或调节化合物的发射波长处的反应介质发射的发光; e)将步骤d)中测量的信号与在仅经受步骤a)和c)的细胞上测量的参考信号进行比较。 用途:检测膜蛋白内化的方法。