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    • 1. 发明授权
    • Fluorescent energy transfer immunoassay
    • 荧光能量转移免疫测定
    • US5631169A
    • 1997-05-20
    • US183238
    • 1994-01-19
    • Joseph R. LakowiczBadri P. MaliwalRichard ThompsonAlvydas Ozinskas
    • Joseph R. LakowiczBadri P. MaliwalRichard ThompsonAlvydas Ozinskas
    • G01N21/64G01N33/542G01N33/543G01N33/58G01N33/533
    • G01N33/582G01N21/6408G01N21/6428G01N33/542G01N2021/6441Y10S436/80
    • A fluorometric luminescence immunoassay method includes forming a sample by exposing a first immune reaction reactant to a second immune reaction reactant capable of reacting with the first reactant, one of the first and second immune reaction reactants being labelled with a photoluminescent energy transfer donor and the other being labelled with a photoluminescent energy transfer acceptor complementary to the photoluminescent donor. At least the photoluminescent donor has the property of photoluminescence, and the photoluminescent donor and acceptor are chosen so that when the first immune reaction reactant reacts with the second immune reaction reactant, the donor and the acceptor are capable of interacting to produce a detectable luminescence lifetime change. The sample is excited with radiation, and the resulting emission is detected. The apparent luminescent lifetime is then calculated to determine the presence of a reaction product of the first and second immune reaction reactants.
    • 荧光发光免疫测定方法包括通过将第一免疫反应反应物暴露于能够与第一反应物反应的第二免疫反应反应物形成样品,第一和第二免疫反应物之一用光致发光能量转移供体标记,另一个 用与光致发光供体互补的光致发光能量转移受体标记。 至少光致发光供体具有光致发光的性质,并且选择光致发光供体和受体,使得当第一免疫反应反应物与第二免疫反应物反应时,供体和受体能够相互作用以产生可检测的发光寿命 更改。 用辐射激发样品,并检测所得到的发射。 然后计算表观发光寿命以确定第一和第二免疫反应物的反应产物的存在。
    • 3. 发明授权
    • Determination of metal ions in solution by photoluminescence anisotropy
    • 通过光致发光各向异性测定溶液中的金属离子
    • US06284544B1
    • 2001-09-04
    • US09071351
    • 1998-04-30
    • Richard B. ThompsonDaniel ElbaumVincent L. FelicciaDavid ChristiansonMarcia W. PatchanZhengfang GeBadri P. Maliwal
    • Richard B. ThompsonDaniel ElbaumVincent L. FelicciaDavid ChristiansonMarcia W. PatchanZhengfang GeBadri P. Maliwal
    • G01N3320
    • G01N33/542G01N21/6445G01N33/20G01N33/582G01N2333/988
    • Homogeneous fluorescence polarization (anisotropy) assays for detecting and quantifying metal ions in solution, based the metal-dependent binding of a fluorescent ligand to an unlabeled macromolecule, or the binding of a metal ion to a fluorescent labeled macromolecule. The metal-dependent binding of a fluorescent ligand to an unlabeled macromolecule (metallo-macromolecule) effects a measurable change in anisotropy as will the binding of metal ions to a fluorescent labeled macromolecule. Binding of the fluorescent ligand to the unlabeled macromolecule is metal dependent with the change in anisotropy being proportional to the concentration of bound metal ions. No binding of the fluorescent ligand to the macromolecule occurs in the absence of metal ions. Conversely, if the fluorescent label is first conjugated to a metallo-macromolecule and the metallo-macromolecule is subsequently stripped of its metal ion, it may then be used to transduce the binding of metal ions. Transduction is provided wherein the covalently bound fluorescent label exhibits changes in anisotropy proportional to the concentration of bound metal ions. In all methods, the change in anisotropy may be simply related to the metal ion concentration of the test solution.
    • 基于荧光配体与未标记的大分子的金属依赖性结合,或金属离子与荧光标记的大分子的结合,用于检测和定量溶液中的金属离子的均匀荧光偏振(各向异性)测定。 荧光配体与未标记的大分子(金属 - 大分子)的金属依赖性结合对金属离子与荧光标记的大分子的结合将产生各向异性的可测量的变化。 荧光配体与未标记的大分子的结合是金属依赖性的,各向异性的变化与结合的金属离子的浓度成比例。 在不存在金属离子的情况下,不发生荧光配体与大分子的结合。 相反,如果荧光标记首先与金属 - 大分子缀合,并且金属 - 大分子随后被其金属离子剥离,则其可用于转导金属离子的结合。 提供转导,其中共价结合的荧光标记表现出与结合的金属离子浓度成比例的各向异性变化。 在各种方法中,各向异性的变化可能与测试溶液的金属离子浓度有关。