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    • 9. 发明申请
    • CHEMICAL ANALYSIS DEVICE
    • 化学分析装置
    • US20090016931A1
    • 2009-01-15
    • US12169968
    • 2008-07-09
    • Taisaku SeinoHiroshi UmetsuMichihiro SaitoTakayuki KandaKumiko Hattori
    • Taisaku SeinoHiroshi UmetsuMichihiro SaitoTakayuki KandaKumiko Hattori
    • G01N35/10B01L3/02
    • G01N35/10B01L3/502G01N2035/103G01N2035/1051G01N2035/1062
    • A chemical analysis device capable of suppressing deterioration of analysis and test accuracy while avoiding contamination by residual samples or reagents and having no complicated configuration is constructed.A pipetting unit is equipped with a syringe, plunger, and needle unit in which a carrier for capturing nucleic acid and a detection cell is mounted on the needle unit. A pipetting unit drive system is configured so that the pipetting unit is detachable. After the detection cell is removed from the pipetting unit and fixed to a nucleic acid amplification detection unit, a suction/dispensing operation of samples/reagents is performed by the pipetting unit and components to be measured are captured by the carrier. Captured components are measured after being dispensed into the detection cell fixed to the nucleic acid amplification detection unit. Then, the detection cell is taken out from the nucleic acid amplification detection unit while mounted on the pipetting unit and the whole pipetting unit is removed from the pipetting unit drive system.
    • 能够抑制分析和测试精度恶化的化学分析装置,同时避免残留的样品或试剂的污染并且没有复杂的结构。 移液单元配备有注射器,柱塞和针单元,其中用于捕获核酸的载体和检测单元安装在针单元上。 移液单元驱动系统被构造成使得移液单元可拆卸。 在从移液单元取出检测单元并固定在核酸扩增检测单元上之后,通过移液单元进行样品/试剂的抽吸/分注操作,由载体捕获要测量的成分。 在分配到固定在核酸扩增检测单元上的检测单元之后,测量捕获的成分。 然后,在安装在移液单元上的情况下,从核酸扩增检测单元取出检测单元,从移液单元驱动系统中取出整个移液单元。
    • 10. 发明申请
    • AUTOMATIC ANALYZER
    • 自动分析仪
    • US20110293473A1
    • 2011-12-01
    • US13145346
    • 2009-12-14
    • Michihiro Saito
    • Michihiro Saito
    • G01N21/76
    • G01N21/6428G01N2021/6439G01N2035/0097
    • An analytic method uses a labeled antigen, labeled antibody, tracer, etc. in which a radio isotope, fluorescent dye, luminescent dye, enzyme, etc. is bonded to an antibody or an antigen bonded to a protein as an object of analysis for performing an assay of a trace amount of a substance such as a hormone, tumor marker, infective pathogen marker, infective antibody, etc., for blood, serum, plasma, or body fluid as a sample or specimen. The analysis is enabled at high sensitivity, with less generation of noises and at low background. When an assay is performed based on the antigen-antibody reaction for a sample in an analytic method by fluorometry or luminometry, detection or measurement of non-specific fluorescence or luminescence such as interference light is eliminated or removed effectively irrespective of the property of the sample or the level of the concentration of substances contained in the sample.
    • 分析方法使用标记的抗原,标记的抗体,示踪剂等,其中放射性同位素,荧光染料,发光染料,酶等与抗体或与蛋白质结合的抗原结合作为分析对象进行 作为样品或样品的血液,血清,血浆或体液的微量物质如激素,肿瘤标志物,感染性病原体标志物,感染性抗体等的测定。 该分析能够在高灵敏度下实现,噪声产生较少,背景较差。 当通过荧光测定或发光测定法在分析方法中基于样品的抗原 - 抗体反应进行测定时,检测或测量非特异性荧光或发光如干涉光,无论样品的性质如何,均可有效地消除或去除 或样品中所含物质的浓度水平。