MICROPARTICLE FRACTIONATION APPARATUS, AND METHOD FOR OPTIMIZING FLUID STREAM IN SAID APPARATUS
    82.
    发明公开
    MICROPARTICLE FRACTIONATION APPARATUS, AND METHOD FOR OPTIMIZING FLUID STREAM IN SAID APPARATUS 有权
    MIKROPARTIKELFRAKTIONIERUNGSVORRICHTUNG和方法的流体流动在这个器件优化

    公开(公告)号:EP2696190A4

    公开(公告)日:2014-09-24

    申请号:EP13768656

    申请日:2013-02-13

    申请人: SONY CORP

    发明人: MURAKI YOSUKE

    IPC分类号: G01N15/14

    摘要: There is provided a microparticle sorting device that automatically optimizes a fluid stream. There is provided a microparticle sorting device that includes a voltage supply unit that supplies a driving voltage to a vibratory element that applies vibration to an orifice that produces a fluid stream, a charge unit that imparts charge to at least some droplets ejected from the orifice, deflecting plates, arranged opposing each other with the fluid stream S therebetween, that vary a travel direction of the droplets, and a first image sensor that acquires an image of the droplets passing between the deflecting plates. The microparticle sorting device is equipped with a controller that detects the droplets in the image, sets a standard band corresponding to a width of the droplets before imparting the charge, and controls the driving voltage of the voltage supply unit so as to further decrease a quantity of the droplets detected in areas within a designated number of pixels from the standard band from among the droplets after imparting the charge.

    Flow cytometer nozzle
    84.
    发明公开
    Flow cytometer nozzle 有权
    Durchflusszytometerdüse

    公开(公告)号:EP2180307A3

    公开(公告)日:2012-10-03

    申请号:EP10001278.0

    申请日:2000-11-29

    申请人: XY, LLC

    IPC分类号: G01N15/14

    摘要: An improved nozzle system for a flow cytometer have been invented for a high efficiency orientation and sorting process of a flat sample and dedicates items such as equine or bovine sperm cells. This improved nozzle system comprises a nozzle (16) with a novel interior surface geometry that can both gently accelerate the cells and can include an elliptical-like, single torsional interior surface element within (c) the nozzle, i.e., a single torsional orientation nozzle (6). The elliptical-like, single torsional interior surface element (e.g.) (8, 9, 10) may have a laminar flow surface and may produce the simplest flow path for applying minimal forces which act in either an accelerative nature or orienting hydrodynamic forces, namely, the single torsional orientation forces, to orient a flat sample (16) such as animal sperm cells into a proper direction for an analyzing and efficiently sorting process in clinical use, for research and for the animal insemination industry.

    Method for controlling one or more parameters of a flow cytometer type measurement system
    86.
    发明公开
    Method for controlling one or more parameters of a flow cytometer type measurement system 审中-公开
    一种用于控制Durchflusszytometermesssystems的一个或多个参数的方法

    公开(公告)号:EP2275799A1

    公开(公告)日:2011-01-19

    申请号:EP10183127.9

    申请日:2004-08-13

    IPC分类号: G01N15/14

    摘要: A method for controlling one or more parameters of a flow cytometer type measurement system, is disclosed. The comprises the following steps
    - measuring a time in which a microsphere (10) travels from a first detection window of the flow cytometer type measurement system to a second detection window of the measurement system; and
    - altering an applied pressure of the measurement system such that the time is substantially constant.

    摘要翻译: 一种用于控制流式细胞计型测量系统的流程的一个或多个参数的方法,是游离缺失盘。 该方法包括以下步骤 - 测量时间,其中,微球(10)从流流式细胞计型测量系统的测量系统的第二探测窗口的第一检测窗口行进; 和 - 检测所述测量系统的施加压力的改变做的时间基本上是恒定的。

    Improved flow cytometer nozzle and flow cytometer sample handling methods
    87.
    发明公开
    Improved flow cytometer nozzle and flow cytometer sample handling methods 有权
    改进的流式细胞仪喷嘴和流式细胞仪样品处理方法

    公开(公告)号:EP2264430A2

    公开(公告)日:2010-12-22

    申请号:EP10182264.1

    申请日:2000-11-29

    申请人: XY, LLC

    IPC分类号: G01N15/14

    摘要: A flow cytometer system, comprising a sample injection tube having an injection point through which a sample may be introduced, a sheath fluid container having a bottom end and wherein said sample injection tube is located within said sheath fluid container, a sheath fluid port connected to said sheath fluid container, a first axial motion surface in a nozzle, a second axial motion surface in said nozzle, a limited maximal acceleration differentiation transition area between said first axial motion surface in said nozzle and said second axial motion surface in said nozzle wherein said limited maximal acceleration differentiation transition area is coordinated with said sample so as to be affirmatively limited to not exceed the practical capabilities of said sample over its length and an analytical system which senses below said nozzle.

    摘要翻译: 一种流式细胞仪系统,包括具有注入点的样本注入管,样本可以通过该注入点引入;鞘液流体容器,具有底端,并且其中所述样本注入管位于所述鞘液流体容器内;鞘流体端口,连接到 所述鞘液容器,喷嘴中的第一轴向运动表面,所述喷嘴中的第二轴向运动表面,所述喷嘴中的所述第一轴向运动表面和所述喷嘴中的所述第二轴向运动表面之间的有限的最大加速度区分过渡区,其中所述 有限的最大加速度区分过渡区域与所述样本协调,以便被肯定地限制为不超过所述样本在其长度上的实际能力以及在所述喷嘴下面感测的分析系统。

    APPARATUS AND METHOD FOR MEASURING THE FLUORESCENCE OF LARGE MULTI-CELLULAR ORGANISMS
    90.
    发明公开
    APPARATUS AND METHOD FOR MEASURING THE FLUORESCENCE OF LARGE MULTI-CELLULAR ORGANISMS 审中-公开
    设备和方法测量荧光BIG多细胞生物

    公开(公告)号:EP2089723A2

    公开(公告)日:2009-08-19

    申请号:EP07873852.3

    申请日:2007-11-13

    发明人: JOHNSON, Paul, E.

    IPC分类号: G01N35/10 G01N15/14 G01N1/00

    摘要: Apparatus and methods for measuring the fluorescence of large multi-cellular organisms in a sample (102, 804) of liquid includes a pumping mechanism, a fluorescence measuring device (104), a method of analyzing (100, 300, 508) the measurements, and optionally, a sorting mechanism (502). The pumping mechanism transfers large multi-cellular organisms from a reservoir (402, 836) through a fluorescence-measuring device (104) causing minimum physical damage and/or stress. The pressure differential driving the organisms from a sample container/reservoir through the measuring device can be derived from gravity (800), air pressure (412), or liquid pressure, or some combination of the three. The fluorescence can be measured in a cytometer using a light detector or imager (106). Generally the detection element will include a filter (114), isolating the wavelength of fluorescent emission. The illumination may be provided by a laser (112) or by an LED (302), combined with the use of dichroic mirrors to allow multiple wavelength simultaneous illumination. In addition, an LED will typically be used with a filter to isolate the optimum excitation wavelength while blocking scattered/reflected LED light from the detection element (but not the fluorescence).