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    • 3. 发明授权
    • Oscillation apparatus and methods for multi-analyte homogeneous fluoro-immunoassays
    • 用于多分析物均匀荧光免疫测定的振荡装置和方法
    • US06242267B1
    • 2001-06-05
    • US09142946
    • 1998-09-18
    • James N. HerronDouglas A. ChristensenScott D. Miles
    • James N. HerronDouglas A. ChristensenScott D. Miles
    • G01N33552
    • G01N33/54386G01N33/54373Y10S435/808Y10S436/807
    • An apparatus and method for rapidly analyzing samples for analytes of interest by an homogeneous immunofluorescence assay. The apparatus includes a sample test cartridge having a high control sample section, a low control sample section, and at least one test sample section. Each of these sections contain at least one pre-loaded reagent housed in a well within the cartridge wherein the low control sample section contains a known low amount of an analyte of interest and the high control sample section contains a known high amount of an analyte of interest. The cartridge includes a biosensor comprising a planar waveguide having first and second parallel plane surfaces and an edge extending between them, the edge having a receiving region for receiving a light beam. Each of the high control sample section, the low control sample section, and the test sample control sections have a well which includes a waveguide surface, wherein the contents of each section contacts capture molecules immobilized on the waveguide surface. The capture molecules are configured to specifically bind a chosen analyte and fluoresce when interacting with light passing through the waveguide surface. The concentration of said analyte of interest in said sample fluid is determined by a comparison of intensities of fluorescence of between said capture molecule areas of said sample capture molecule well, said low control capture molecule well, and said high control capture molecule well.
    • 用于通过均匀免疫荧光测定快速分析感兴趣的分析物的样品的装置和方法。 该装置包括具有高控制样品部分,低对照样品部分和至少一个测试样品部分的样品测试盒。 这些部分中的每一个包含至少一个预先加载的试剂,其容纳在筒内的孔中,其中低对照样品部分含有已知的低量感兴趣的分析物,并且高对照样品部分含有已知的大量分析物 利益。 所述盒包括生物传感器,所述生物传感器包括具有第一和第二平行平面的平面波导和在它们之间延伸的边缘,所述边缘具有用于接收光束的接收区域。 高控制采样部分,低控制样品部分和测试样品控制部分中的每一个具有包括波导表面的阱,其中每个部分的内容物接触固定在波导表面上的捕获分子。 捕获分子被配置为特异性地结合所选择的分析物并且当与通过波导表面的光相互作用时发出荧光。 通过比较所述样品捕获分子阱的所述捕获分子区域,所述低对照捕获分子阱和所述高对照捕获分子阱之间的荧光强度来确定所述样品流体中所述目标分析物的浓度。
    • 4. 发明授权
    • Method of assaying pyrrole-containing biological compounds
    • 测定含吡咯生物化合物的方法
    • US06667180B2
    • 2003-12-23
    • US09970328
    • 2001-10-03
    • Jeffrey D. BradySimon P. Robins
    • Jeffrey D. BradySimon P. Robins
    • G01N33552
    • C07D495/04G01N33/6887Y10S436/815Y10T436/145555
    • This invention relates to a method of assaying pyrrole-containing biological compounds and chemical compositions that can be used in the method. The method involves contacting a biological compound with one of: a) a bound or bindable derivatizing agent which forms a reaction product with the biological compound, followed by exposure to a detectable molecule which forms a complex with the reaction product; or b) a derivatizing agent which forms a reaction product with the biological compound, followed by exposure to a bound binding agent specific to the biological compound in the reaction product; or c) a binding agent specific to the biological compound, followed by exposure to a derivatizing agent which forms a reaction product with the biological compound, and determining the amount of bound biological compound. There is also provided a method of preparing an antigen.
    • 本发明涉及可用于该方法的含吡咯生物化合物和化学组成的测定方法。 该方法包括使生物化合物与以下物质之一接触:a)与生物化合物形成反应产物的结合或可结合的衍生化试剂,然后暴露于与反应产物形成络合物的可检测分子; orb)与生物化合物形成反应产物的衍生剂,然后暴露于反应产物中对生物化合物特异的结合结合剂; orc)对生物化合物特异性的结合剂,然后暴露于与生物化合物形成反应产物的衍生化试剂,并测定结合的生物化合物的量。 还提供了制备抗原的方法。