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    • 2. 发明授权
    • Particles for diagnostic and therapeutic use
    • 用于诊断和治疗用途的颗粒
    • US07709273B2
    • 2010-05-04
    • US11273275
    • 2005-11-14
    • Sharat SinghJohn S. PeaseJacqueline SadakianDaniel B. WagnerEdwin F. Ullman
    • Sharat SinghJohn S. PeaseJacqueline SadakianDaniel B. WagnerEdwin F. Ullman
    • G01N33/543G01N31/00
    • G01N33/587C12Q1/6816Y10T436/10C12Q2563/155C12Q2523/319
    • Methods, compositions and kits are disclosed. The compositions are light emitting and comprise a polymeric matrix having dissolved therein a photoactive compound. The composition has the characteristic that, after activation of the photoactive compound, the rate of decrease in the intensity of light emission at any time during a 20-fold decrease in the intensity is proportional to the intensity of the light emission. In one embodiment the polymeric matrix is comprised of particles of about 20 nm to about 100 μm in diameter to which is bound a specific binding pair member. The particles generally comprise a polymeric matrix having dissolved therein about 1 to about 20% by weight of a dopant. The compositions may be used in methods for determining an analyte. A combination is provided comprising (1) a medium suspected of containing the analyte, (2) and the aforementioned composition. The photoactive substance is activated and the effect of the activating on the optical properties of the combination is detected. The presence and amount of the effect is related to the presence and amount of the analyte in the medium. Also disclosed are kits for use in an assay.
    • 公开了方法,组合物和试剂盒。 组合物是发光的并且包含其中溶解有光敏化合物的聚合物基质。 该组合物具有以下特征:在光活性化合物活化后,强度降低20倍的任何时间的发光强度的降低率与发光强度成比例。 在一个实施方案中,聚合物基质包含直径约20nm至约100μm的颗粒,其与特定结合对构件结合。 颗粒通常包含其中溶解约1至约20重量%的掺杂剂的聚合物基质。 该组合物可用于测定分析物的方法中。 提供的组合包括(1)怀疑含有分析物的介质,(2)和上述组合物。 光活性物质被激活,并且检测到激活对组合的光学性质的影响。 影响的存在和数量与介质中分析物的存在和数量有关。 还公开了用于测定的试剂盒。
    • 5. 发明授权
    • Method of calibration with photoactivatable chemiluminescent matrices
    • 用光活化化学发光基质校准的方法
    • US5618732A
    • 1997-04-08
    • US434617
    • 1995-05-04
    • John S. PeaseHrair KirakossianDaniel B. WagnerEdwin F. Ullman
    • John S. PeaseHrair KirakossianDaniel B. WagnerEdwin F. Ullman
    • G01N33/532G01N21/78G01N33/58G01N21/64G01N21/76
    • G01N33/582Y10S435/81Y10S436/829Y10S436/905Y10T436/10
    • Methods for labeling a material are disclosed. The methods comprise combining with the material (a) a photosensitizer capable upon irradiation of generating singlet oxygen and (b) a chemiluminescent compound capable of being activated by singlet oxygen wherein the photosensitizer and the chemiluminescent compound are incorporated in a particulate matrix or a non-particulate solid matrix. The particulate matrix can be solid or fluid. The methods allow for generating delayed luminescence, which can be realized upon irradiation of the matrix. The methods have application to the determination of an analyte in a medium suspected of containing the analyte. One method comprises subjecting a medium suspected of containing an analyte to conditions under which a complex of specific binding pair (sbp) members is formed in relation to the presence of the analyte and determining whether the sbp member complex has formed by employing as a label a single composition having both chemiluminescent and photosensitizer properties. Upon activation of the photosensitizer property singlet oxygen is generated and activates the chemiluminescent property. Compositions and kits are also disclosed.
    • 公开了标记材料的方法。 所述方法包括与材料(a)结合,所述光敏剂能够在产生单线态氧的照射时和(b)能够被单线态氧活化的化学发光化合物,其中光敏剂和化学发光化合物掺入颗粒基质或非均相中, 颗粒状固体基质。 颗粒基质可以是固体或流体。 这些方法允许产生延迟发光,这可以在照射基质时实现。 该方法可用于确定怀疑含有分析物的介质中的分析物。 一种方法包括使怀疑含有分析物的培养基相对于分析物的存在形成特异性结合对(sbp)成员的复合物的条件,以及通过使用标记a来确定sbp成员复合物是否形成 具有化学发光和光敏剂性质的单一组合物。 激活光敏剂时,产生单线态氧并激活化学发光性能。 还公开了组合物和试剂盒。
    • 7. 发明授权
    • Photoactivatable chemiluminescent matrices
    • 光活化化学发光基质
    • US5709994A
    • 1998-01-20
    • US470862
    • 1995-06-06
    • John S. PeaseHrair KirakossianDaniel B. WagnerEdwin F. Ullman
    • John S. PeaseHrair KirakossianDaniel B. WagnerEdwin F. Ullman
    • G01N33/532G01N21/78G01N33/58G01N33/52C09K11/00C12Q1/00C12Q1/68
    • G01N33/582Y10S435/81Y10S436/829Y10S436/905Y10T436/10
    • Methods for labeling a material are disclosed. The methods comprise combining with the material (a) a photosensitizer capable upon irradiation of generating singlet oxygen and (b) a chemiluminescent compound capable of being activated by singlet oxygen wherein the photosensitizer and the chemiluminescent compound are incorporated in a particulate matrix or a non-particulate solid matrix. The particulate matrix can be solid or fluid. The methods allow for generating delayed luminescence, which can be realized upon irradiation of the matrix. The methods have application to the determination of an analyte in a medium suspected of containing the analyte. One method comprises subjecting a medium suspected of containing an analyte to conditions under which a complex of specific binding pair (sbp) members is formed in relation to the presence of the analyte and determining whether the sbp member complex has formed by employing as a label a single composition having both chemiluminescent and photosensitizer properties. Upon activation of the photosensitizer property singlet oxygen is generated and activates the chemiluminescent property. Compositions and kits are also disclosed.
    • 公开了标记材料的方法。 所述方法包括与材料(a)结合,所述光敏剂能够在产生单线态氧的照射时和(b)能够被单线态氧活化的化学发光化合物,其中光敏剂和化学发光化合物掺入颗粒基质或非均相中, 颗粒状固体基质。 颗粒基质可以是固体或流体。 这些方法允许产生延迟发光,这可以在照射基质时实现。 该方法可用于确定怀疑含有分析物的介质中的分析物。 一种方法包括使怀疑含有分析物的培养基相对于分析物的存在形成特异性结合对(sbp)成员的复合物的条件,以及通过使用标记a来确定sbp成员复合物是否形成 具有化学发光和光敏剂性质的单一组合物。 激活光敏剂时,产生单线态氧并激活化学发光性能。 还公开了组合物和试剂盒。
    • 9. 发明授权
    • Methods for single nucleotide polymorphism detection
    • 单核苷酸多态性检测方法
    • US06632606B1
    • 2003-10-14
    • US09592053
    • 2000-06-12
    • Edwin F. UllmanSharat Singh
    • Edwin F. UllmanSharat Singh
    • C12Q168
    • C12Q1/6827C12Q1/6834C12Q2565/519C12Q2535/125C12Q2563/179C12Q2563/131
    • Methods and compositions are provided for determining large numbers of single nucleotide polymorphisms in target DNA employing particles having (1) primers complementary to sequences in the target DNA where the next succeeding 3′-nucleotide is a potential single nucleotide polymorphism and coding composition members, where the members are unique for each primer, and (2) differentially labeled terminating nucleotides, where the label permits separation of the terminating nucleotides. Desirably the particles are separated into groups having a common prevalent next succeeding nucleotide. The particles and target DNA are combined under nucleotide extending conditions, the particles separated into groups in accordance with the terminating nucleotide and the coding members identified, so that one knows the sequence and the single nucleotide polymorphism. Various protocols are provided for the determination.
    • 提供了用于使用具有(1)与目标DNA中的序列互补的引物,其中下一个后续的3'-核苷酸是潜在的单核苷酸多态性和编码组成成员的粒子来确定靶DNA中大量单核苷酸多态性的方法和组合物,其中 成员对于每个引物是独特的,和(2)差异标记的终止核苷酸,其中标记允许分离终止的核苷酸。 理想地,将颗粒分离成具有普通的下一个后续核苷酸的基团。 颗粒和靶DNA在核苷酸延伸条件下合并,根据终止的核苷酸和鉴定的编码成员将颗粒分成组,以便知道序列和单核苷酸多态性。 提供各种协议用于确定。