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    • 3. 发明授权
    • Fixative and staining solutions
    • 固定和染色方案
    • US08445284B2
    • 2013-05-21
    • US13526164
    • 2012-06-18
    • Daniel LapenKerri Licari
    • Daniel LapenKerri Licari
    • G01N31/00
    • G01N1/30Y10T436/10Y10T436/101666Y10T436/108331Y10T436/25
    • The formulations, systems, and methods disclosed herein permit automated preparation of specimens (e.g., biological specimens) for examination. The formulations can include a cytological fixative solution including Azure B, a surfactant, methanol, and ethylene glycol. The disclosed formulations, systems, and methods provide fast, efficient, and highly uniform specimen processing using minimal quantities of fluids. The methods include at least a fixing phase for fixing a specimen to a substrate such as a microscope slide, a staining phase for staining the specimen, and a rinsing phase for rinsing the specimen. One or more of the fixing, staining, and rinsing phases include one or more agitation phases for distributing reagents evenly and uniformly across the specimen. The systems can be implemented as a standalone device or as a component in a larger system for preparing and examining specimens.
    • 本文公开的制剂,系统和方法允许自动制备样品(例如,生物样品)用于检查。 制剂可以包括包括Azure B,表面活性剂,甲醇和乙二醇的细胞学固定溶液。 所公开的配方,系统和方法使用最少量的流体提供快速,有效和高度均匀的样品处理。 该方法至少包括用于将样品固定到诸如显微镜载片的基底的固定阶段,用于染色样品的染色阶段和用于漂洗样品的漂洗阶段。 固定,染色和漂洗阶段中的一个或多个包括一个或多个用于均匀均匀地分布试剂的搅拌相。 这些系统可以作为独立设备或作为更大系统中用于准备和检查样本的组件来实现。
    • 9. 发明申请
    • SAMPLE TRANSPORT SYSTEMS AND METHODS
    • 样本运输系统和方法
    • US20130020175A1
    • 2013-01-24
    • US13548844
    • 2012-07-13
    • Brian J. McKeenEric D. YeatonJames L. Dowling
    • Brian J. McKeenEric D. YeatonJames L. Dowling
    • B65G37/00
    • G01N35/04G01N1/31G01N35/00029G01N35/0099G01N35/02G01N2035/00039G01N2035/041
    • Sample transport systems are described that move a sample carrier from one station to a next station in a sample processing systems. The systems include: a translating member; two or more sample carrier retaining devices attached to the translating member, wherein each of the two or more sample carrier retaining devices can include a retainer portion to temporarily retain one or more sample carriers; and a movement mechanism to move the translating member and the attached sample carrier retaining devices between a first position and a second position; wherein the sample carrier retaining devices are controlled and moved simultaneously to retain a sample carrier when the translating member reaches the first position and to release a sample carrier when the translating member reaches the second position to successively advance sample carriers in the sample processing systems.
    • 描述了样本传送系统,其将样本载体从样本处理系统中的一个站移动到下一个站。 系统包括:翻译成员; 两个或更多个样品载体保持装置附接到平移构件,其中两个或更多个样品载体保持装置中的每一个可以包括暂时保持一个或多个样品载体的保持器部分; 以及移动机构,用于在第一位置和第二位置之间移动所述平移构件和附接的样品载体保持装置; 其中当所述平移构件到达所述第一位置时,所述样品载体保持装置被同时控制和移动以保持样品载体,并且当所述平移构件到达所述第二位置时释放样品载体,以连续地提取所述样品处理系统中的样品载体。
    • 10. 发明授权
    • Measuring volume and constituents of cells
    • 测量细胞体积和成分
    • US08339586B2
    • 2012-12-25
    • US13446996
    • 2012-04-13
    • Michael ZahniserRussell Zahniser
    • Michael ZahniserRussell Zahniser
    • G01N33/48G06K9/00A61B5/00
    • G01N15/0227G01N15/1475G01N33/49G01N2015/0073G01N2015/1472G06K9/00127G06K9/0014G06T7/62G06T2207/10056G06T2207/30024
    • A method of determining a volume of a platelet includes: (a) illuminating the platelet with incident light at a plurality of illumination wavelengths; (b) obtaining at least one two-dimensional image of the platelet corresponding to each illumination wavelength; (c) for each illumination wavelength, determining a mean optical density and a maximum optical density for the platelet; (d) determining an area of the platelet; (e) for each illumination wavelength, determining a volume of the platelet; (f) for each illumination wavelength, determining an integrated optical density for the platelet; and (g) determining the volume of the platelet based on a weighted combination of the area of the platelet, the volumes of the platelet corresponding to each of the illumination wavelengths, and the integrated optical densities for the platelet corresponding to each of the illumination wavelengths.
    • 确定血小板体积的方法包括:(a)用多个照明波长的入射光照射血小板; (b)获得对应于每个照明波长的血小板的至少一个二维图像; (c)对于每个照明波长,确定血小板的平均光密度和最大光密度; (d)确定血小板的面积; (e)对于每个照明波长,确定血小板的体积; (f)对于每个照明波长,确定血小板的综合光密度; 和(g)基于血小板面积,对应于每个照明波长的血小板的体积和对应于每个照明波长的血小板的积分光密度的加权组合来确定血小板的体积 。