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    • 1. 发明申请
    • Method for eliminating crosstalk between waveguide grating-based biosensors located in a microplate and the resulting microplate
    • 用于消除位于微板中的基于波导光栅的生物传感器与所得微板之间的串扰的方法
    • US20060229818A1
    • 2006-10-12
    • US11101096
    • 2005-04-07
    • Ye FangAnn FerrieNorman FontaineAnthony FrutosEric MozdyChuan-Che WangPo Yuen
    • Ye FangAnn FerrieNorman FontaineAnthony FrutosEric MozdyChuan-Che WangPo Yuen
    • G06F19/00
    • G01N21/7743G01N21/253
    • The present invention includes several methods for modifying the current processes of manufacturing optical sensing microplates that use continuous waveguide films to reduce/eliminate crosstalk between the biosensors that are incorporated within wells. The methods include (1) physically deteriorating/removing the waveguide film between individual biosensors; (2) chemically depositing highly absorbing materials within the waveguide film between individual biosensors; (3) patterning disordered (scattering) regions between the diffraction gratings that define individual biosensors; (4) using a specific mask and depositing individual patches of waveguide film, where each patch defines at least one biosensor. Each of these methods and several other methods described herein prevent the propagation of light between individual sensing regions, thereby eliminating optical crosstalk between the biosensors. The present invention also includes the resulting microplate.
    • 本发明包括几种用于修改制造光学感测微板的当前工艺的方法,其使用连续波导膜来减少/消除结合在孔内的生物传感器之间的串扰。 所述方法包括(1)在各个生物传感器之间物理劣化/去除波导膜; (2)在各个生物传感器之间在波导膜内化学沉积高吸收材料; (3)在限定单个生物传感器的衍射光栅之间图形化无序(散射)区域; (4)使用特定掩模并沉积波导膜的各个贴片,其中每个贴片限定至少一个生物传感器。 这些方法和本文所描述的其它方法中的每一种都防止光在各个感测区域之间的传播,从而消除了生物传感器之间的光学串扰。 本发明还包括所得到的微孔板。
    • 3. 发明申请
    • System and method for performing G protein coupled receptor (GPCR) cell assays using waveguide-grating sensors
    • 使用波导光栅传感器进行G蛋白偶联受体(GPCR)细胞测定的系统和方法
    • US20060223051A1
    • 2006-10-05
    • US11100262
    • 2005-04-05
    • Ye FangAnn FerrieNorman FontaineJoydeep LahiriPo Yuen
    • Ye FangAnn FerrieNorman FontaineJoydeep LahiriPo Yuen
    • G01N33/53C12Q1/00
    • G01N33/5041G01N21/4788G01N21/553G01N2333/726G01N2500/10
    • The present invention includes a system and method that uses optical LID biosensors to monitor in real time agonist-induced GPCR signaling events within living cells. Particularly, the present invention includes a system and method for using an optical LID biosensor to screen compounds against a target GPCR within living cells based on the mass redistribution due to agonist-induced GPCR activation. In an extended embodiment, the present invention discloses different ways for self-referencing the optical LID biosensor to eliminate unwanted sensitivity to ambient temperature, pressure fluctuations, and other environmental changes. In yet another extended embodiment, the present invention discloses different ways for screening multiple GPCRs in a single type of cell or multiple GPCRs in multiple types of cells within a single medium solution. In still yet another extended embodiment, the present invention discloses different ways to confirm the physiological or pharmacological effect of a compound against a specific GPCR within living cells.
    • 本发明包括使用光学LID生物传感器实时监测活细胞内激动剂诱导的GPCR信号事件的系统和方法。 特别地,本发明包括使用光学LID生物传感器基于由于激动剂诱导的GPCR活化导致的质量再分布来筛选活细胞内的靶GPCR的化合物的系统和方法。 在扩展实施例中,本发明公开了用于自参考光学LID生物传感器以消除对环境温度,压力波动和其他环境变化的不期望的灵敏度的不同方式。 在又一个扩展的实施方案中,本发明公开了在单一培养基溶液中的多种类型的细胞中单种类型细胞或多种GPCR筛选多种GPCR的不同方式。 在又一个延伸的实施方案中,本发明公开了确定化合物对活细胞内特异性GPCR的生理或药理作用的不同方式。