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    • 7. 发明授权
    • Scanning probe microscope
    • 扫描探针显微镜
    • US07954165B2
    • 2011-05-31
    • US12095953
    • 2006-10-12
    • Toshio AndoMitsuru SakashitaTakayuki Uchihashi
    • Toshio AndoMitsuru SakashitaTakayuki Uchihashi
    • G01Q10/06G01Q60/34
    • G01Q60/32G01Q10/065Y10S977/851
    • A scanning probe microscope is provided, which can be stably used for a long time even if excitation efficiency varies during scan. A cantilever (5) is excited, and the cantilever (5) and a sample are subjected to relative scanning. A second-harmonic component detection circuit (31) detects second-harmonic component amplitude of oscillation of the cantilever (5) as integral-multiple component amplitude. The second-harmonic component amplitude is amplitude of a second-harmonic component having a frequency twice as high as excitation frequency. An excitation intensity adjustment circuit (33) controls excitation intensity based on the detected second-harmonic component amplitude such that the second-harmonic component amplitude is kept constant.
    • 提供扫描探针显微镜,其即使在扫描期间激发效率变化也可以长时间稳定使用。 悬臂(5)被激发,并且悬臂(5)和样品进行相对扫描。 二次谐波分量检测电路(31)将悬臂(5)的振荡的二次谐波分量振幅检测为积分 - 多分量振幅。 二次谐波分量幅度是具有激励频率的两倍的频率的二次谐波分量的振幅。 励磁强度调节电路(33)基于所检测到的二次谐波分量振幅来控制激励强度,使得二次谐波分量振幅保持恒定。
    • 10. 发明授权
    • Device and method of use for detection and characterization of pathogens and biological materials
    • 用于检测和表征病原体和生物材料的装置和方法
    • US06897015B2
    • 2005-05-24
    • US10160372
    • 2002-05-30
    • Eric R. HendersonSaju R. NettikadanCurtis L. Mosher
    • Eric R. HendersonSaju R. NettikadanCurtis L. Mosher
    • B05D3/00C12Q1/02C12Q1/68C12Q1/70G01N33/552G01N33/553G01N33/554G01N33/569G01Q10/00G01Q30/20G01Q60/34G02B26/10
    • G01N33/553G01N33/56983G01N2333/07Y10S977/853
    • The present invention includes a method and apparatus for the detection of a target material. The method and apparatus includes providing a substrate with a surface and forming a domains of deposited materials thereon. The deposited material can be placed on the surface and bound directly and non-specifically to the surface, or it may be specifically or non-specifically bound to the surface. The deposited material has an affinity for a specific target material. The domains thus created are termed affinity domains or deposition domains. Multiple affinity domains of deposited materials can be deposited on a single surface, creating a plurality of specific binding affinity domains for a plurality of target materials. Target materials may include, for example, pathogens or pathogenic markers such as viruses, bacteria, bacterial spores, parasites, prions, fungi, mold or pollen spores. The device thus created is incubated with a test solution, gas or other supporting environment suspected of containing one or more of the target materials. Specific binding interactions between the target materials and a particular affinity domain occurs and is detected by various methods.
    • 本发明包括用于检测目标材料的方法和装置。 该方法和装置包括提供具有表面的基底并在其上形成沉积材料的区域。 沉积的材料可以放置在表面上并且非特异性地结合到表面上,或者可以特异性地或非特异性地结合到表面上。 沉积材料对特定靶材料具有亲和力。 由此产生的结构域称为亲和结构域或沉积域。 沉积材料的多个亲和性结构域可以沉积在单个表面上,为多个目标材料产生多个特异性结合亲和结构域。 靶物质可包括例如病原体或致病性标志物,例如病毒,细菌,细菌孢子,寄生虫,朊病毒,真菌,霉菌或花粉孢子。 将如此产生的装置与怀疑含有一种或多种目标材料的测试溶液,气体或其它支持环境一起温育。 目标材料与特定亲和力域之间的特异性结合相互作用发生并通过各种方法检测。