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    • 3. 发明申请
    • INTRACELLULAR COMPLEXES AS BIOMARKERS
    • 细胞内复合物作为生物标志物
    • WO2004087887A2
    • 2004-10-14
    • PCT/US2004009805
    • 2004-03-30
    • ACLARA BIOSCIENCES INCSINGH SHARATBADAL M YOUSSOUFJIN XUENGUANGSALIMI-MOOSAVI HOSSEIN
    • SINGH SHARATBADAL M YOUSSOUFJIN XUENGUANGSALIMI-MOOSAVI HOSSEIN
    • A61B20060101C07K16/28C12N20060101C12Q3/00G01N33/542G01N33/543G01N33/574C12N
    • G01N33/57492C07K16/2863G01N33/542G01N2333/485G01N2800/52
    • The invention provides a method for determining a disease status of a patient by measuring expression levels of selected intracellular complexes. In one aspect of the invention, the activation status of apoptotic pathways in a patient sample is determined by measuring relative amounts of protein-protein complexes that are characteristic of the apoptotic pathways. In particular, the invention provides a method of determining the activation status of the mitochondrial apoptotic pathway by simultaneously measuring relative amounts of complexes between 14-3-3 proteins and BAD proteins on the one hand and complexes of Bcl-2 proteins and BAD proteins on the other hand. Preferably, methods of the invention are implemented by using sets of binding compounds having releasable molecular tags that are specific for multiple components of one or more complexes formed within apoptotic pathways. After binding molecular tags are released and separated from the assay mixture for analysis.
    • 本发明提供了一种通过测量所选细胞内复合物的表达水平来确定患者的疾病状态的方法。 在本发明的一个方面,通过测量凋亡通路特征的蛋白质 - 蛋白质复合物的相对量来确定患者样品中凋亡途径的活化状态。 特别地,本发明提供了一种通过同时测量14-3-3蛋白和BAD蛋白之间的复合物的相对量以及Bcl-2蛋白和BAD蛋白的复合物的相对量来确定线粒体凋亡途径的激活状态的方法 另一方面。 优选地,本发明的方法通过使用具有可释放分子标签的结合化合物组来实现,所述可释放分子标签对在凋亡途径内形成的一种或多种复合物的多种组分是特异性的。 结合分子标签后,从测定混合物中分离出分子标签进行分析。
    • 4. 发明申请
    • PHOTOACTIVATION DEVICE AND METHOD
    • 摄影装置及方法
    • WO2003051669A1
    • 2003-06-26
    • PCT/US2002/040442
    • 2002-12-18
    • ACLARA BIOSCIENCES, INC.BJORNSON, Torleif, O.KIRAKOSSIAN, HrairBROWN, Albert, W., Jr.WEVERS, WilliamSALIMI-MOOSAVI, Hossein
    • BJORNSON, Torleif, O.KIRAKOSSIAN, HrairBROWN, Albert, W., Jr.WEVERS, WilliamSALIMI-MOOSAVI, Hossein
    • B60Q1/06
    • A61N5/062A61N2005/0652
    • A photoactivation apparatus (200) separately delivers light to a plurality of wells of a multiwell plate (110). The device includes a plurality of light emitting diodes (210) attached to a first surface of a substrate (220) such that when the photoactivation apparatus is positioned on the multiwell plate each of the light emitting diodes delivers light to one corresponding well. The light emitting diodes (210) may extend at least partially into the wells of the multiwell plate. A heat sink (250) and fan may be provided on the device to dissipate heat generated by the light emitting diodes. The components are preferably enclosed in a conveniently-sized housing (270). The housing may include one or more grips and air vents. The apparatus includes an interlocking lip (230) defining a recess which is sized to receive at least a portion of the multiwell plate. A power supply connected to the apparatus and configured to provide an equal voltage across each of the light emitting diodes.
    • 光活化装置(200)分别将光传送到多孔板(110)的多个孔。 该装置包括附接到基板(220)的第一表面的多个发光二极管(210),使得当光致活化装置位于多孔板上时,每个发光二极管将光传送到一个相应的孔。 发光二极管(210)可以至少部分地延伸到多孔板的孔中。 可以在设备上提供散热器(250)和风扇以散发由发光二极管产生的热量。 部件优选地封闭在方便尺寸的壳体(270)中。 房屋可以包括一个或多个把手和通风口。 该装置包括限定凹部的互锁唇缘(230),凹部的尺寸设置成容纳多孔板的至少一部分。 连接到该装置并被配置成在每个发光二极管上提供相等电压的电源。
    • 5. 发明申请
    • METHODS AND COMPOSITIONS FOR ANALYZING PROTEINS
    • 分析蛋白质的方法和组合物
    • WO2002095356A2
    • 2002-11-28
    • PCT/US2002/016098
    • 2002-05-21
    • ACLARA BIOSCIENCES, INC.SINGH, SharatSALIMI-MOOSAVI, HosseinTAHIR, Syed, HasanWALLWEBER, Gerald, J.KIRAKOSSIAN, HrairMATRAY, Tracy, J.HERNANDEZ, Vincent, S.
    • SINGH, SharatSALIMI-MOOSAVI, HosseinTAHIR, Syed, HasanWALLWEBER, Gerald, J.KIRAKOSSIAN, HrairMATRAY, Tracy, J.HERNANDEZ, Vincent, S.
    • G01N
    • G01N33/6842C07K16/00C07K2317/40G01N33/582G01N33/6803
    • Methods, compositions and kits are disclosed for determining one or more target polypeptides in a sample where the target polypeptides have undergone a post-translational modification. A mixture comprising the sample and a first reagent comprising a cleavage-inducing moiety and a first binding agent for a binding site on a target polypeptide is subjected to conditions under which binding of respective binding moieties occurs. The binding site is the result of post-translational modification activity involving the target polypeptide. The method may be employed to determine the target polypeptide itself. In another embodiment the presence and/or amount of the target polypeptide is related to the presence and/or amount and/or activity of an agent such as an enzyme involved in the post-translational modification of the target polypeptide. The interaction between the first binding agent and the binding site brings the cleavage-inducing moiety into close proximity to a cleavable moiety, which is associated with the polypeptide and is susceptible to cleavage only when in proximity to the cleavage-inducing moiety. In this way, an electrophoretic tag for each of the polypeptides may be released. Released electrophoretic tags are separated and the presence and/or amount of the target polypeptides are determined based on the corresponding electrophoretic tags.
    • 公开了用于确定样品中一种或多种靶多肽已经经历了翻译后修饰的方法,组合物和试剂盒。 包含样品和包含切割诱导部分的第一试剂和用于靶多肽上的结合位点的第一结合剂的混合物经受各自结合部分的结合发生的条件。 结合位点是涉及靶多肽的翻译后修饰活性的结果。 该方法可用于确定靶多肽本身。 在另一个实施方案中,靶多肽的存在和/或量与试剂例如涉及靶多肽的翻译后修饰的酶的存在和/或量和/或活性有关。 第一结合剂和结合位点之间的相互作用导致切割诱导部分紧密接近可切割部分,其可与多肽相关,并且仅在接近切割诱导部分时易于切割。 以这种方式,可以释放每个多肽的电泳标签。 分离出释放的电泳标签,并且基于相应的电泳标签确定靶多肽的存在和/或量。
    • 7. 发明申请
    • ERBB SURFACE RECEPTOR COMPLEXES AS BIOMARKERS
    • ERBB表面受体复合物作为生物标志物
    • WO2004091384A3
    • 2005-12-29
    • PCT/US2004009715
    • 2004-03-30
    • ACLARA BIOSCIENCES INCCHAN-HUI PO-YINGSALIMI-MOOSAVI HOSSEINSHI YININGSINGH SHARATDUA RAJIVMUKHERJEE ALIPIDAPARTHI SAILAJA
    • CHAN-HUI PO-YINGSALIMI-MOOSAVI HOSSEINSHI YININGSINGH SHARATDUA RAJIVMUKHERJEE ALIPIDAPARTHI SAILAJA
    • A61B20060101C07K16/28C12N20060101C12Q3/00G01N33/542G01N33/543G01N33/574
    • G01N33/57492C07K16/2863G01N33/542G01N2333/485G01N2800/52
    • The invention is directed to a new class of biomarker in patient samples comprising dimers of ErbB cell surface membrane receptors. In one aspect, the invention includes a method of determining the status of a disease or healthful condition by correlating such condition to amounts of one or more dimers of ErbB cell surface membrane receptors measured directly in a patient sample, in particular a fixed tissue sample. In another aspect, the invention includes a method of determining a status of a cancer in a specimen from an individual by correlating measurements of amounts of one or more dimers of ErbB cell surface membrane receptors in cells of the specimen to such status, including presence or absence of a pre-cancerous state, presence or absence of a cancerous state, prognosis of a cancer, or responsiveness to treatment. Preferably, methods of the invention are implemented by using sets of binding compounds having releasable molecular tags that are specific for multiple components of one or more types of receptor dimers. After binding, molecular tags are released and separated from the assay mixture for analysis.
    • 本发明涉及包含ErbB细胞表面膜受体的二聚体的患者样品中的新一类生物标志物。 在一个方面,本发明包括通过将这样的病症与在患者样品,特别是固定组织样品中直接测量的一种或多种ErbB细胞表面膜受体的二聚体的量相关联来确定疾病或健康状况的状态的方法。 另一方面,本发明包括通过将样本细胞中的ErbB细胞表面膜受体的一种或多种二聚体的量的测量值与这样的状态相关联来确定来自个体的样品中癌症状态的方法,包括存在或 不存在癌前状态,存在或不存在癌症状态,癌症预后或对治疗的反应性。 优选地,本发明的方法通过使用具有可释放分子标签的结合化合物来实现,所述组合化合物对于一种或多种类型的受体二聚体的多种组分是特异性的。 结合后,分离标签被释放并与测定混合物分离,用于分析。