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    • 21. 发明申请
    • Chemiluminescence analyzer
    • 化学发光分析仪
    • US20030148536A1
    • 2003-08-07
    • US10067501
    • 2002-02-04
    • Chi-Wang LiangJeng-Fong Chiou
    • G01N021/76
    • G01N21/76G01N2201/0231G01N2201/0253
    • A chemiluminescence analyzer determines the level of chemiluminescence of a specimen. The chemiluminescence analyzer includes a light detection chamber for containing the specimen to be analyzed. The light detection chamber includes a chamber access device, for allowing the positioning of the specimen within the light detection chamber, and a shutter device. The shutter device and the chamber access device are configured to each have an open position and a closed position. A light detector is positioned behind the shutter device. When the shutter device is in the open position, the light detector detects light within the light detection chamber. An interlock assembly is interfaced with the shutter device and the chamber access device, such that the interlock assembly prevents the shutter device and the chamber access device from being simultaneously opened.
    • 化学发光分析仪确定样品的化学发光水平。 化学发光分析仪包括用于容纳要分析的样品的光检测室。 光检测室包括用于允许样本在光检测室内定位的室进入装置和快门装置。 快门装置和室进入装置被构造成各具有打开位置和关闭位置。 光检测器位于快门装置后面。 当快门装置处于打开位置时,光检测器检测光检测室内的光。 互锁组件与快门装置和腔室进入装置接口,使得互锁组件防止快门装置和腔室进入装置同时打开。
    • 22. 发明申请
    • Method of measuring the luminescence emitted in a luminescent assay
    • 测量在发光测定中发出的发光的方法
    • US20020177235A1
    • 2002-11-28
    • US10008549
    • 2001-11-13
    • Michel MabileGerard MathisEtienne Jean-Pierre JoluDominique PouyatChristophe Dumont
    • G01N021/76
    • G01N21/6452G01N21/6428G01N33/54306G01N33/582
    • The present invention relates to a method of measuring the luminescence emitted in a luminescent assay, which makes it possible to correct certain perturbations due to the measuring medium. Said method comprises employing at least one luminescent tracer compound and a luminescent compound used as an internal reference, which, when exposed to the same excitation wavelength, are capable of emitting at different wavelengths, null2 and null1 respectively, either by direct luminescence or by the induction of a luminescent emission, and correcting the measurement of the luminescence emitted by the tracer compound at wavelength null2 on the basis of the measurement of the luminescence emitted by the reference compound at wavelength nulll. The invention further relates to the use of said method in a homogeneous method of detecting and/or determining an analyte, and to a device for carrying it out.
    • 本发明涉及一种测量在发光测定中发出的发光的方法,其使得可以校正由于测量介质引起的某些扰动。 所述方法包括使用至少一种发光示踪剂化合物和用作内部参考的发光化合物,当暴露于相同的激发波长时,其能够分别通过直接发光或通过直接发光分别发射不同波长的lambd2和lambd1 诱导发光发射,并且基于在参考化合物在波长lambd1处发出的发光的测量来校正在波长lambd2下由示踪剂化合物发射的发光的测量。 本发明还涉及所述方法在检测和/或确定分析物的均匀方法中的用途以及用于将其分离出来的装置。
    • 25. 发明申请
    • Chemiluminescence-based microfluidic biochip
    • 基于化学发光的微流体生物芯片
    • US20020123059A1
    • 2002-09-05
    • US10022007
    • 2001-12-13
    • Winston Z. Ho
    • C12Q001/68G01N021/76
    • B01L3/5027B01L3/50273B01L2200/10B01L2200/16B01L2300/0636B01L2300/0654B01L2300/0816B01L2300/0864B01L2300/0867B01L2300/087B01L2300/0887B01L2400/0481B01L2400/0487B01L2400/0683C12Q2565/629G01N21/76G01N21/7703
    • The disclosure describes how to use luminescence detection mechanism, move microfluid, and control multiple-step biochemical reactions in closed confined microfluidic biochip platform. More particularly, a self-contained disposable biochip with patterned microchannels and compartments having storage means for storing a plurality of samples, reagents, and luminescent substrates. At least one external microactuator in the biochip system produces positive pressure and automates multiple-step reactions in microfluidic platforms for clinical chemistry, cell biology, immunoassay and nucleic acid analysis. The method comprises the steps of transferring sequentially at least one of samples, reagents, and then luminescent substrate from compartments through microchannels to reaction sites. The luminescent substrates react with probes to form a probe complex resulting into luminescence, which is detected by an optical detector.
    • 本发明描述了如何使用发光检测机制,移动微流体,并在封闭的微流体生物芯片平台中控制多步生化反应。 更具体地,具有图案化微通道和隔间的独立的一次性生物芯片具有用于存储多个样品,试剂和发光基底的存储装置。 生物芯片系统中的至少一个外部微致动器产生正压力并在微流体平台中自动化多步反应用于临床化学,细胞生物学,免疫分析和核酸分析。 该方法包括以下步骤:将来自隔室的样品,试剂,然后将发光底物中的至少一种顺序地通过微通道转移到反应位点。 发光底物与探针反应形成探针复合物,产生发光,由光学检测器检测。
    • 26. 发明申请
    • Method for determining chemical reactivity
    • 测定化学反应性的方法
    • US20020110919A1
    • 2002-08-15
    • US09972520
    • 2001-10-05
    • Larry C. WienkersMichael J. HauerDennis E. Epps
    • G01N021/76
    • G01N21/6428G01N21/75G01N33/68G01N2021/6417G01N2500/00Y10T436/13
    • A method for screening chemical compounds for electrophilic properties comprising the steps of: (a) providing an assay having one or more reaction vessels; (b) adding a predetermined amount of separate chemical compounds for screening to each reaction vessel; (c) adding a predetermined amount of a surrogate chemical marker to each reaction vessel and allowing said separate chemical compounds and surrogate chemical marker to incubate for a period of time; (d) adding a reactive chemical to each reaction vessel which is capable of reacting with residual surrogate chemical marker such that the amount of residual surrogate chemical marker present after step (c) can be quantitatively or qualitatively measured; and (e) quantitatively or qualitatively measuring said residual chemical marker is provided.
    • 一种用于筛选亲电性质的化合物的方法,包括以下步骤:(a)提供具有一个或多个反应容器的测定; (b)向每个反应容器中加入预定量的用于筛选的单独化学化合物; (c)向每个反应容器中加入预定量的替代化学标记物,并允许所述单独的化合物和替代化学品标记物孵育一段时间; (d)向能够与残留替代化学标记物反应的每个反应容器中加入反应性化学物质,使得步骤(c)之后存在的残留替代化学标记物的量可以定量或定性测量; 并提供(e)定量或定性测量所述残留化学标记物。