会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 5. 发明申请
    • MULTI-DIRECTIONAL IMMUNOCHROMATOGRAPHIC ASSAYS
    • 多方向免疫印迹测定
    • WO2007024633A3
    • 2007-06-07
    • PCT/US2006032200
    • 2006-08-17
    • RESPONSE BIOMEDICAL CORPHARRIS PAUL CRICHARDS BRIAN G
    • HARRIS PAUL CRICHARDS BRIAN G
    • G01N33/558
    • G01N33/558
    • Methods for quantitatively measuring the amount of one or more analyte(s) of interest in a fluid sample, and kits useful in the methods, are disclosed. The methods involve providing a solid phase apparatus comprising a membrane having an application point, a sample capture zone, and a control capture zone, where the sample capture zone and the control capture zone are approximately equidistant from the application point; and providing a sample collection apparatus comprising one or more population(s) of analyte binding particles. In the assays, a fluid sample is introduced into the sample collection apparatus, and the resultant mixture is applied to the application point of the membrane. The fluid allows transport components of the assay by capillary action to and through the sample capture zone(s) and the control capture zone. The amount of each analyte of interest in the fluid sample is related (e.g., either directly or inversely) to a corrected particle amount, which can be determined, for example, as a ratio of the amount of particles in the corresponding sample capture zone and the amount of particles in the control capture zone.
    • 公开了用于定量测量流体样品中感兴趣的一种或多种分析物的量的方法和用于该方法的试剂盒。 该方法包括提供一种固相装置,其包括具有应用点的膜,样品捕获区和对照捕获区,其中样品捕获区和对照捕获区与施加点大致相等; 以及提供包含一个或多个分析物结合颗粒群的样品收集装置。 在测定中,将流体样品引入样品收集装置中,并将所得混合物施加到膜的施加点。 流体允许通过毛细管作用将测定的运输成分传送到样品捕获区域和控制捕获区域。 流体样品中感兴趣的每个分析物的量与校正的颗粒量相关(例如,直接或反向),其可以例如确定为相应样品捕获区中的颗粒的量与 控制捕获区域中的颗粒数量。
    • 9. 发明申请
    • MULTI-DIRECTIONAL IMMUNOCHROMATOGRAPHIC ASSAYS
    • 多方向免疫层析法测定
    • WO2007024633A2
    • 2007-03-01
    • PCT/US2006/032200
    • 2006-08-17
    • RESPONSE BIOMEDICAL CORPORATIONHARRIS, Paul, C.RICHARDS, Brian, G.
    • HARRIS, Paul, C.RICHARDS, Brian, G.
    • G01N33/50
    • G01N33/558
    • Methods for quantitatively measuring the amount of one or more analyte(s) of interest in a fluid sample, and kits useful in the methods, are disclosed. The methods involve providing a solid phase apparatus comprising a membrane having an application point, a sample capture zone, and a control capture zone, where the sample capture zone and the control capture zone are approximately equidistant from the application point; and providing a sample collection apparatus comprising one or more population(s) of analyte binding particles. In the assays, a fluid sample is introduced into the sample collection apparatus, and the resultant mixture is applied to the application point of the membrane. The fluid allows transport components of the assay by capillary action to and through the sample capture zone(s) and the control capture zone. The amount of each analyte of interest in the fluid sample is related (e.g., either directly or inversely) to a corrected particle amount, which can be determined, for example, as a ratio of the amount of particles in the corresponding sample capture zone and the amount of particles in the control capture zone.
    • 公开了用于定量测量流体样品中一种或多种感兴趣分析物的量的方法以及在这些方法中有用的试剂盒。 所述方法包括提供包含膜的固相装置,所述膜具有施用点,样品捕获区和对照捕获区,其中所述样品捕获区和所述对照捕获区与所述施加点大致等距离; 并提供包含一个或多个分析物结合颗粒群的样品收集装置。 在测定中,将流体样品引入到样品收集装置中,并将所得混合物施加到膜的施加点。 流体通过毛细管作用允许测定的转运组分通过和通过样品捕获区和对照捕获区。 流体样本中的每种感兴趣分析物的量与校正的粒子量相关(例如,直接或相反),其可以例如被确定为相应样本捕获区中的粒子的量与 控制捕获区中的颗粒数量。
    • 10. 发明申请
    • COMPENSATION FOR VARIABILITY IN SPECIFIC BINDING IN QUANTITATIVE ASSAYS
    • 对定量测定中特定结合的变异性的补偿
    • WO2002077646A1
    • 2002-10-03
    • PCT/US2002/008284
    • 2002-03-14
    • RESPONSE BIOMEDICAL CORPORATIONHARRIS, Paul, C.RICHARDS, Brian, G.
    • HARRIS, Paul, C.RICHARDS, Brian, G.
    • G01N33/543
    • G01N33/558G01N33/54386
    • Methods for quantitatively measuring the amount of an analyte of interest in a fluid sample are disclosed. The methods involve providing a membrane having an application, a contact region comprising analyte-binding particles, a sample capture zone, and a control capture zone, where the contact region is between the application point and the sample capture zone, and the sample capture region is between the contact region and the control capture zone (Figure 1).In the assays, a fluid allows transport components of the assay by capillary action through the contact region, to and through the sample capture zone and subsequently to and through the control capture zone. In a "sandwich assay" embodiment, the amount of analyte in the fluid sample is related to a corrected analyte-binding particle amount, which can be determined, for example, as a ratio of the amount of analyte-binding particles in the sample capture zone and the amount of analyte-binding particles on the control capture zone. In a "competitive assay" embodiment, the amountof analyte in the fluid sample is inversely related to a corrected analyte-coated particle amount, which can be determinedas a ratio of the amount of analyte-coated particles in the sample capture zone and the amount of analyte-coated particles in the control capture zone.
    • 公开了用于定量测量流体样品中目标分析物的量的方法。 所述方法包括提供具有应用的膜,包含分析物结合颗粒的接触区域,样品捕获区域和控制捕获区域,其中接触区域在施加点和样品捕获区域之间,并且样品捕获区域 在接触区域和控制捕获区之间(图1)。 在测定中,流体允许通过毛细管作用通过接触区域,到并通过样品捕获区域并随后通过控制捕获区域将分析物的传输成分。 在“夹心测定”实施方案中,流体样品中的分析物的量与校正的分析物结合粒子量相关,其可以例如由样品捕获中的分析物结合颗粒的量的比例确定 区域和对照捕获区域上的分析物结合颗粒的量。 在“竞争性测定”实施方案中,流体样品中的分析物与构建的分析物涂覆的颗粒量成反比,其可以被确定为样品捕获区域中分析物包被的颗粒的量与 对照捕获区域中分析物包被的颗粒的量。