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    • 81. 发明申请
    • METHOD AND SYSTEM FOR DETECTING FLUOROCHROMES IN A FLOW CYTOMETER
    • 用于检测流式细胞仪中荧光素的方法和系统
    • US20110204259A1
    • 2011-08-25
    • US13033299
    • 2011-02-23
    • Clare E. RogersJack T. BallCollin A. Rich
    • Clare E. RogersJack T. BallCollin A. Rich
    • G01J1/58
    • G01N15/1429G01N15/1459
    • A method for detecting fluorochromes in a flow cytometer, including: receiving a sample including particles each tagged with at least one of a first fluorochrome and a second fluorochrome, in which the first and second fluorochromes having distinct spillover coefficients; detecting the particles, including detecting the first and second fluorochromes with a first detector and a second detector; forming a data set for detected particles based on the detection of the first and second fluorochromes; characterizing a detected spillover coefficient for each detected fluorochrome from the data set; and sorting the detected particles into predicted fluorochrome populations based on the detected spillover coefficients. A system for detecting fluorochromes in a flow cytometer, including a flow cell, a fixed gain detection system, and a processor that generates a detected spillover coefficient for each detected particle and sorts the detected particle into predicted fluorochrome populations based on the detected spillover coefficient.
    • 一种用于在流式细胞仪中检测荧光染料的方法,包括:接收包含每个标记有第一荧光染料和第二荧光染料中的至少一种的颗粒的样品,其中第一和第二荧光染料具有不同的溢出系数; 检测颗粒,包括用第一检测器和第二检测器检测第一和第二荧光染料; 基于第一和第二荧光色素的检测形成检测到的颗粒的数据集; 表征来自数据集的每个检测到的荧光染料的检测到的溢出系数; 并且基于检测到的溢出系数将检测到的颗粒分选成预测的荧光染色体群体。 一种用于在流式细胞仪中检测荧光染料的系统,包括流动池,固定增益检测系统和处理器,其产生每个检测到的颗粒的检测到的溢出系数,并且基于检测到的溢出系数将检测到的颗粒分解成预测的荧光染色体群。
    • 87. 发明申请
    • METHOD OF PUMPING QUANTUM DOTS
    • 泵浦量的方法
    • US20110133100A1
    • 2011-06-09
    • US12961631
    • 2010-12-07
    • Patanjali KambhampatiRyan CooneySamuel Sewall
    • Patanjali KambhampatiRyan CooneySamuel Sewall
    • G01J1/58B82Y99/00
    • H01L31/035281B82Y20/00B82Y30/00H01L31/0304H01L31/035236H01L31/073H01L31/1828H01L31/1852Y02E10/543Y02E10/544
    • Strongly confined semiconductor quantum dots theoretically offer for broadband and continuous tunability of their emitting wavelength based upon simply varying the particle size. However, prior art consistently has demonstrated a lower particle size limit below which optical gain cannot be achieved, for example 2.3 nm for CdSe in toluene. As such the prior art points to combinations of alternative materials and host media as the route to achieving the goal of broadband emission sources using quantum dots. However, according to the invention optical gain can be achieved in quantum dots below these previous experimental limits by resonantly pumping the quantum dots to a specific excitonic state, i.e. electron position relative to the quantum dot, such that the multiexcitonic interferences are minimized. Using this approach optical gain in CdSe of R=2.1 nm and 1.5 nm has been demonstrated in the yellow/amber region of the visible spectrum.
    • 理论上强烈的限制半导体量子点基于简单地改变粒度来提供其发射波长的宽带和连续可调性。 然而,现有技术一直表现出较低的粒径限度,在此以下,不能实现光学增益,例如在甲苯中的CdSe为2.3nm。 因此,现有技术指出替代材料和主机介质的组合作为实现使用量子点的宽带发射源目标的途径。 然而,根据本发明,通过将量子点共振地泵浦到特定的激子态,即相对于量子点的电子位置,可以在低于这些先前实验极限的量子点中实现光学增益,使得多谐振干扰被最小化。 使用这种方法,在可见光谱的黄色/琥珀色区域已经证明了在R = 2.1nm和1.5nm的CdSe中的光学增益。
    • 88. 发明申请
    • TOTAL REFLECTION FLUORESCENCE OBSERVATION DEVICE
    • 总反射荧光观察装置
    • US20110121204A1
    • 2011-05-26
    • US13055854
    • 2009-05-20
    • Nobutaka KumazakiSatoshi TakahashiHirokazu KatoTakanovu Haga
    • Nobutaka KumazakiSatoshi TakahashiHirokazu KatoTakanovu Haga
    • G01J1/58
    • G01N21/648G02B21/16
    • A technique and device for fluorescence observation with good operability, high sensitivity, acid high reliability. The device is used for fluorescence observation using evanescent light. The angle of incidence of the excitation light is adjusted so that the excitation light is always totally reflected from the surface of a substrate irrespective of the angle of the surface of the substrate. The method includes a step of shining the excitation light on the observation substrate while continuously varying the angle of the excitation light with respect to the observation substrate, a step of sensing the shone excitation light by means of optical sensors, and a step of setting the angle of total reflection according to the result of the sensing by the optical sensors. The direction in which the shone excitation light travels varies with the angle of incidence. That is, the excitation light travels as the transmitted light, the reflected light, or the surface propagating light. These lights are sensed by the corresponding optical sensors, and how the angle of incidence of the excitation light is with respect to the critical angle is determined. The angle of incidence of the excitation light is varied depending on the result of the determination, thereby realizing an optimum total reflection angle.
    • 用于荧光观察的技术和装置,操作性好,灵敏度高,酸度高可靠性。 该器件用于使用ev逝光的荧光观察。 调节激发光的入射角,使得激发光始终从基板的表面全反射,而与基板的表面的角度无关。 该方法包括在观察基板上照射激发光的步骤,同时连续地改变激发光相对于观察基板的角度,通过光学传感器感测照射激发光的步骤,以及将 根据光学传感器的感测结果,全反射角度。 照射激发光的行进方向随入射角而变化。 也就是说,激发光作为透射光,反射光或表面传播光行进。 这些光被相应的光学传感器感测,并且确定激发光的入射角相对于临界角如何。 激发光的入射角取决于确定的结果而变化,从而实现最佳的全反射角。
    • 89. 发明申请
    • Optical Fiber Imaging System And Method For Generating Fluorescence Imaging
    • 光纤成像系统及产生荧光成像的方法
    • US20110121202A1
    • 2011-05-26
    • US12623973
    • 2009-11-23
    • Ming-Jun LiShenping Li
    • Ming-Jun LiShenping Li
    • G01J1/58
    • G01J3/10G01J3/4406H01S3/0057H01S3/0675H01S3/06754H01S3/06791H01S3/2383
    • A nonlinear fluorescence imaging system and method for generating fluorescence imaging includes a pulsed laser source for generating laser pulses at a first wavelength and an optical pulse stretcher including one or more optical pulse stretcher fibers having a first dispersion parameter at the first wavelength. The system also includes a probe for interfacing with a sample to deliver the laser pulses and extract fluorescence signals excited in the sample. One or more optical delivery fibers are included for delivering the laser pulses and collecting nonlinear fluorescence signals. The optical delivery fiber has a second dispersion parameter at the first wavelength which is opposite a polarity of the first dispersion parameter. A detector detects images based on the collected fluorescence signals.
    • 用于产生荧光成像的非线性荧光成像系统和方法包括用于产生第一波长的激光脉冲的脉冲激光源和包括具有第一波长的第一色散参数的一个或多个光脉冲展宽光纤的光脉冲展宽器。 该系统还包括用于与样品接口以传送激光脉冲并提取在样品中激发的荧光信号的探针。 包括一个或多个光学传递光纤用于传送激光脉冲和收集非线性荧光信号。 光传送光纤具有与第一色散参数的极性相反的第一波长的第二色散参数。 检测器基于收集的荧光信号检测图像。
    • 90. 发明申请
    • LASER SCANNING MICROSCOPE
    • 激光扫描显微镜
    • US20110121198A1
    • 2011-05-26
    • US12948937
    • 2010-11-18
    • Tatsuo NakataKosuke TAKAGI
    • Tatsuo NakataKosuke TAKAGI
    • G01J1/58
    • G02B21/004G02B21/0076G02B21/008
    • Provided is a laser scanning microscope with which it is possible to reduce the time required for scanning and to detect light from a sample with high sensitivity. Provided is a laser scanning microscope 100 including a stage 20 that moves a sample 19 placed thereon, a laser light source 1 that emits laser light L, a line-focus optical system 3 that focuses the laser light L into a line shape, a DMD 7 including a plurality of movable micromirrors that are arrayed in the lengthwise direction of the line and that reflect the line-focused laser light L, an irradiation optical system 2 that irradiates the sample 19 with the laser light L reflected by the DMD 7, and a photodetector 17 in which a plurality of channels for detecting light from the sample 19 are arrayed in one column, wherein the DMD 7 is driven so that a plurality of movable micromirrors simultaneously reflect the laser light L and so that the movable micromirrors that reflect the laser light L are sequentially switched, and the stage 20 moves the sample 19 in a direction crossing the array direction of a plurality of light spots formed on the sample 19.
    • 提供了一种激光扫描显微镜,其可以减少扫描和从高灵敏度的样品检测光所需的时间。 提供了一种激光扫描显微镜100,其包括移动放置在其上的样品19的载物台20,发射激光L的激光源1,将激光L聚焦成线状的线聚焦光学系统3,DMD 7包括沿线的长度方向排列并反射线聚焦激光L的多个可移动微镜;照射光学系统2,其用由DMD 7反射的激光L照射样品19;以及 其中用于检测来自样品19的光的多个通道被布置在一列中的光电检测器17,其中驱动DMD 7,使得多个可移动微镜同时反射激光L,并且使得反射 激光L依次切换,台20沿着与样品19上形成的多个光点的排列方向交叉的方向移动样品19。