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    • 4. 发明申请
    • METHODS AND COMPOSITIONS TO DETECT A BIOLOGICAL ACTIVITY
    • 检测生物活性的方法和组合物
    • US20130230876A1
    • 2013-09-05
    • US13883620
    • 2011-10-28
    • Stephen B. RoscoeKurt J. HalversonJesse D. MillerStephanie J. MoellerJason W. Bjork
    • Stephen B. RoscoeKurt J. HalversonJesse D. MillerStephanie J. MoellerJason W. Bjork
    • G01N21/64
    • G01N21/6486C12Q1/04
    • Compositions that comprise water, a first indicator reagent that can be converted by a first biological activity to a first biological derivative, and a plurality of particles are provided. The first indicator reagent can comprise a fluorogenic enzyme substrate having a fluorophore selected from the group consisting of umbelliferone, 7-aminocoumarin, β-naphthylamine, β-naphthol, fluorescein, resorufin, 9H-(1,3-dichloro-9,9-dimethyl acridin-2-one), rhodamine 110, a derivative of any of the foregoing fluorophores, and a combination of any of the foregoing fluorophores. The particles are capable of receiving and retaining the first biological derivative from an aqueous liquid. The first biological derivative can be indicative of a microorganism. The compositions further can comprise a gelling agent. Methods of using the compositions to detect the presence or absence of a microorganism in a sample are also provided.
    • 提供了包含水,可以通过第一生物活性转化为第一生物衍生物的第一指示剂试剂和多个颗粒的组合物。 第一指示剂可以包括具有选自伞形酮,7-氨基香豆素,β-萘胺,β-萘酚,荧光素,再次吸收的9H-(1,3-二氯-9,9-四氢 - 二甲基吖啶-2-酮),罗丹明110,任何前述荧光团的衍生物,以及任何上述荧光团的组合。 颗粒能够从水性液体中接收和保留第一生物衍生物。 第一种生物衍生物可以指示微生物。 组合物还可以包含胶凝剂。 还提供了使用组合物来检测样品中微生物的存在或不存在的方法。
    • 7. 发明授权
    • Methods and compositions to detect a biological activity
    • 检测生物活性的方法和组合物
    • US09435739B2
    • 2016-09-06
    • US13883620
    • 2011-10-28
    • Stephen B. RoscoeKurt J. HalversonJesse D. MillerStephanie J. MoellerJason W. Bjork
    • Stephen B. RoscoeKurt J. HalversonJesse D. MillerStephanie J. MoellerJason W. Bjork
    • C12Q1/44G01N21/64C12Q1/04
    • G01N21/6486C12Q1/04
    • Compositions that comprise water, a first indicator reagent that can be converted by a first biological activity to a first biological derivative, and a plurality of particles are provided. The first indicator reagent can comprise a fluorogenic enzyme substrate having a fluorophore selected from the group consisting of umbelliferone, 7-aminocoumarin, β-naphthylamine, β-naphthol, fluorescein, resorufin, 9H-(1,3-dichloro-9,9-dimethyl acridin-2-one), rhodamine 110, a derivative of any of the foregoing fluorophores, and a combination of any of the foregoing fluorophores. The particles are capable of receiving and retaining the first biological derivative from an aqueous liquid. The first biological derivative can be indicative of a microorganism. The compositions further can comprise a gelling agent. Methods of using the compositions to detect the presence or absence of a microorganism in a sample are also provided.
    • 提供了包含水,可以通过第一生物活性转化为第一生物衍生物的第一指示剂试剂和多个颗粒的组合物。 第一指示剂可以包含具有选自伞形酮,7-氨基香豆素,β-萘胺,β-萘酚,荧光素,再利用者,9H-(1,3-二氯-9,9-四氢 - 二甲基吖啶-2-酮),罗丹明110,任何前述荧光团的衍生物,以及任何上述荧光团的组合。 颗粒能够从水性液体中接收和保留第一生物衍生物。 第一种生物衍生物可以指示微生物。 组合物还可以包含胶凝剂。 还提供了使用组合物来检测样品中微生物的存在或不存在的方法。
    • 8. 发明授权
    • Methods of determining the amount of microorganisms present in a test sample
    • 确定测试样品中存在的微生物量的方法
    • US08518664B2
    • 2013-08-27
    • US13513794
    • 2010-12-17
    • Stephen B. RoscoePhillip A. BoleaStephanie J. Moeller
    • Stephen B. RoscoePhillip A. BoleaStephanie J. Moeller
    • C12Q1/04
    • G01N21/643C12Q1/04C12Q1/06
    • Methods of determining the amount of microorganisms present in a test sample. The methods include a) incubating the test sample with a growth media to form an incubated sample, wherein the growth media includes an enzyme substrate and the enzyme substrate includes an enzymatically hydrolyzable group and a fluorescent group, wherein microorganisms present in the test sample include an enzyme that hydrolyzes the hydrolyzable group from the fluorescent group to form a fluorescently detectable product, wherein the fluorescently detectable product has both an acidic and basic species; b) exciting the fluorescently detectable product with light having a wavelength of Exλiso for a time sufficient for the fluorescently detectable product to emit light, wherein Exλiso is the absorbance isosbestic point of the fluorescently detectable product; c) detecting light emitted at a wavelength of Emλ1; and d) quantifying the light emitted at the wavelength of Emλ1, wherein the quantity of the light emitted at the wavelength Emλ1 is indicative of the amount of microorganisms present in the test sample.
    • 确定测试样品中存在的微生物量的方法。 所述方法包括:a)用生长培养基孵育所述测试样品以形成孵育的样品,其中所述生长培养基包括酶底物,并且所述酶底物包括酶促水解基团和荧光基团,其中存在于所述测试样品中的微生物包括 从荧光基团水解可水解基团以形成荧光检测产物的酶,其中荧光检测产物具有酸性和碱性物质; b)用具有Exlambdaiso波长的光激发荧光检测产物足够的荧光检测产物发光的时间,其中Exlambdaiso是荧光检测产物的吸光度等值点; c)检测在波长λ1处发射的光; 以及d)量化在λ1波长处发射的光,其中在波长λ1处发射的光的量指示测试样品中存在的微生物的量。
    • 9. 发明申请
    • METHODS OF DETECTING MICROORGANISMS AND KITS THEREFORE
    • 检测微生物和试剂盒的方法
    • US20120252049A1
    • 2012-10-04
    • US13513794
    • 2010-12-17
    • Stephen B. RoscoePhillip A. BoleaStephanie J. Moeller
    • Stephen B. RoscoePhillip A. BoleaStephanie J. Moeller
    • G01N21/64C12M1/34
    • G01N21/643C12Q1/04C12Q1/06
    • A method of detecting microorganisms in a test sample is provided. The method includes the steps of: a) incubating the test sample with a growth media to form an incubated sample, wherein the growth media includes an enzyme substrate and the enzyme substrate includes an enzymatically hydrolysable group and a fluorescent group, wherein microorganisms present in the test sample include an enzyme that hydrolyzes the hydrolysable group from the fluorescent group to form a fluorescently detectable product, wherein the fluorescently detectable product has both an acidic and basic species; b) exciting the fluorescently detectable product with light having a wavelength of Exλiso for a time sufficient for the fluorescently detectable product to emit light, wherein Exλiso is the absorbance isosbestic point of the fluorescently detectable product; and c) detecting light emitted at a wavelength of Emλ1.
    • 提供了一种检测试样中微生物的方法。 该方法包括以下步骤:a)用生长培养基孵育测试样品以形成孵育的样品,其中生长培养基包括酶底物,酶底物包括酶促水解基团和荧光基团,其中存在于 测试样品包括从荧光基团水解可水解基团以形成荧光可检测产物的酶,其中荧光检测产物具有酸性和碱性物质; b)用具有Exλiso波长的光激发荧光检测产物足够的荧光检测产物发光的时间,其中Exλiso是荧光检测产物的吸光度等值点; 以及c)检测在Emλ1的波长处发射的光。