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    Method of detecting hematopoietic progenitor cells
    1.
    再颁专利
    Method of detecting hematopoietic progenitor cells 有权
    检测造血祖细胞的方法

    公开(公告)号：USRE39006E1

    公开(公告)日：2006-03-07

    申请号：US10704463

    申请日：2003-11-07

    申请人： Berend Houwen ,  Yukio Tsujino ,  Takashi Morikawa ,  Yoshiro Ikeuchi ,  Yukio Hamaguchi ,  Fu-sheng Wang ,  Kojiro Hirai

    发明人： Berend Houwen ,  Yukio Tsujino ,  Takashi Morikawa ,  Yoshiro Ikeuchi ,  Yukio Hamaguchi ,  Fu-sheng Wang ,  Kojiro Hirai

    IPC分类号： C12Q1/04

    CPC分类号： G01N33/5094

    摘要： Improved method for detecting and/or counting the appearance of hematopoietic progenitor cells which comprises the steps of mixing a blood sample with a reagent capable of detecting immature cells without employing any immunological techniques, obtaining cell information about the thus treated sample using a particle analyzer and constructing a cell distribution profile, delineating a portion of the profile as a zone in which at least one subclass of hematopoietic progenitor cells appear, and counting the cells within the zone. The method is capable of detecting the appearance of hematopoietic progenitor cells in a simple and positive manner.

    摘要翻译： 用于检测和/或计数造血祖细胞外观的改进方法，其包括以下步骤：将血液样品与能够检测未成熟细胞的试剂混合而不使用任何免疫技术，使用粒子分析仪获得关于如此处理的样品的细胞信息; 构建细胞分布轮廓，将轮廓的一部分描绘为其中存在至少一个造血祖细胞亚类的区域，并对该区域内的细胞进行计数。 该方法能够以简单和积极的方式检测造血祖细胞的外观。

    Diluting reagent and method compelling time-independent consistency in MCV assay
    3.
    发明授权
    Diluting reagent and method compelling time-independent consistency in MCV assay 有权
    稀释试剂和方法在MCV测定中引人注目的时间依赖性一致性

    公开(公告)号：US06225124B1

    公开(公告)日：2001-05-01

    申请号：US09323689

    申请日：1999-06-02

    申请人： Berend Houwen ,  Kinya Uchihashi ,  Yukio Hamaguchi ,  Rolf Mast

    发明人： Berend Houwen ,  Kinya Uchihashi ,  Yukio Hamaguchi ,  Rolf Mast

    IPC分类号： G01N3348

    CPC分类号： G01N33/5094 ,  G01N15/12 ,  Y10T436/10 ,  Y10T436/101666 ,  Y10T436/108331 ,  Y10T436/2525 ,  Y10T436/25625

    摘要： Aqueous blood-sample diluting reagent and method of its use for compelling a morphological change in a blood sample to yield an MCV value assayed at elapsed time after the sample is drawn to be consistent within a diagnostically acceptable range with the original, immediate post-drawing MCV value. Selection of a small amount of a predetermined surfactant added within a limited range of concentration, and of a salt for adjusting osmotic pressure of the sample is thereby determined. The blood sample is treated with an anti-coagulant agent immediately post-drawing, and for assay in a particle analyzer at post-drawing elapsed time is diluted with the reagent solution. The reagent has an osmotic pressure (&pgr;) of approximately 150-400 mOsm/kg and a pH of 6.0-8.5. The surfactant is present in a 0.0005% to 0.5% concentration and has a hydrophile-lipophile balance (HLB) of 10-20.

    摘要翻译： 水性血液样品稀释试剂及其用于强制血液样品中形态学变化的方法，以产生在样品抽出后经过时间测定的MCV值，使其在诊断上可接受的范围内与原始的立即后绘图 MCV值。 由此确定少量在有限浓度范围内加入的预定表面活性剂和用于调节样品渗透压的盐的选择。 血液样品立即在拉伸后用抗凝剂处理，并且在抽出后经过时间的粒子分析仪中用试剂溶液稀释。 试剂的渗透压（pI）为约150-400mOsm / kg，pH为6.0-8.5。 表面活性剂的浓度为0.0005％至0.5％，亲水亲油平衡（HLB）为10-20。

    Process for discriminating and counting erythroblasts
    4.
    发明授权
    Process for discriminating and counting erythroblasts 失效
    红细胞鉴别和计数的方法

    公开(公告)号：US06911313B2

    公开(公告)日：2005-06-28

    申请号：US09058323

    申请日：1998-04-09

    申请人： Berend Houwen ,  Fu-sheng Wang ,  Tomohiro Tsuji ,  Takashi Sakata ,  Yukio Hamaguchi

    发明人： Berend Houwen ,  Fu-sheng Wang ,  Tomohiro Tsuji ,  Takashi Sakata ,  Yukio Hamaguchi

    IPC分类号： G01N33/50 ,  G01N33/569 ,  G01N33/80 ,  G01N33/53 ,  G01N21/76

    CPC分类号： G01N33/5094 ,  G01N15/1459 ,  G01N33/56972 ,  G01N33/80 ,  G01N2015/1006 ,  G01N2015/1402 ,  Y10T436/107497 ,  Y10T436/108331 ,  Y10T436/13 ,  Y10T436/25125 ,  Y10T436/2525 ,  Y10T436/25375

    摘要： A method for discriminating and counting erythroblasts comprises the steps of: (i) staining leukocytes in a hematologic sample by adding a fluorescent labeled antibody capable of binding specifically with leukocytes to the hematologic sample; (ii) raising the permeability only of cell membranes of erythroblasts in the hematologic sample to a nucleotide fluorescent dye which does not permeate a cell membrane usually, the nucleotide fluorescent dye having a fluorescent spectrum capable of being distinguished from that of a fluorescent labeling compound of the fluorescent labeled antibody in step (i); (iii) staining nuclei of the erythroblasts in the hematologic sample with the nucleotide fluorescent dye; (iv) subjecting the hematologic sample to flowcytometry to detect at least two fluorescent signals from each cell; and (v) discriminating and counting the erythroblasts from difference in intensity between the at least two fluorescent signals.

    摘要翻译： 用于鉴别和计数红细胞的方法包括以下步骤：（i）通过将能够与白细胞特异性结合的荧光标记抗体加入到血液样品中来染色血液学样品中的白细胞; （ii）将血液学样品中的红细胞的细胞膜的渗透性提高至不透过细胞膜的核苷酸荧光染料，所述核苷酸荧光染料具有与荧光标记化合物的荧光标记化合物不同的荧光光谱 步骤（i）中的荧光标记抗体; （iii）用核苷酸荧光染料染色血液样品中的红细胞核; （iv）使血液样品经流式细胞术检测来自每个细胞的至少两个荧光信号; 和（v）鉴别和计数红细胞与至少两个荧光信号之间的强度差异。

    Method for classifying and counting leukocytes
    5.
    发明授权
    Method for classifying and counting leukocytes 失效
    白细胞分类和计数方法

    公开(公告)号：US06900023B1

    公开(公告)日：2005-05-31

    申请号：US09388899

    申请日：1999-09-02

    申请人： Berend Houwen ,  Fu-sheng Wang ,  Hiroyuki Fujimoto ,  Takashi Sakata ,  Yukio Hamaguchi

    发明人： Berend Houwen ,  Fu-sheng Wang ,  Hiroyuki Fujimoto ,  Takashi Sakata ,  Yukio Hamaguchi

    IPC分类号： G01N33/49 ,  G01N15/14 ,  G01N33/50 ,  G01N33/53 ,  G01N33/536 ,  G01N33/569

    CPC分类号： G01N33/56972 ,  G01N33/5094 ,  G01N2333/70546 ,  Y10S435/962 ,  Y10S436/80 ,  Y10S436/824 ,  Y10S436/825 ,  Y10T436/101666 ,  Y10T436/107497 ,  Y10T436/13 ,  Y10T436/25 ,  Y10T436/25125

    摘要： A method for classifying and counting leukocytes comprises the steps of: (1) adding to a hematological sample the following fluorescence-labeled antibodies labeled with fluorescent dyes which emit fluorescences distinguishable from each other; (a) a first fluorescence-labeled antibody (1st antibody) which bonds specifically to leukocytes, (b) a second fluorescence-labeled antibody (2nd antibody) which bonds to at least one kind of neutrophilic cells, and (c) a third fluorescence-labeled antibody (3rd antibody) which bonds to at least one kind of immature granulocytic cells, in order to stain leukocytic cells in the sample, and removing erythrocytes from the sample; (2) analyzing the resulting sample using a flow cytometer to measure at least one scattered light signal and three separate fluorescence signals; (3) defining a group of granulocytic cells on the basis of intensity of the scattered light and intensity of fluorescence from the 1st antibody; (4) defining neutrophilic cells in the defined group of granulocylic cells on the basis of the intensity of the fluorescence from the 1st antibody and intensity of fluorescence from the 2nd or 3rd antibody; (5) classifying the defined group of the neutrophilic cells into groups of neutrophilic cells different in degree of maturity on the basis of the intensity of the fluorescence from the 2nd antibody and the intensity of the fluorescence from the 3rd antibody, and counting the number of cells in each of the groups.

    摘要翻译： 用于白细胞分类和计数的方法包括以下步骤：（1）向血液样品中加入以荧光染料标记的荧光标记的抗体，所述荧光染料发射荧光彼此区分; （a）与白细胞特异性结合的第一荧光标记抗体（第一抗体），（b）与至少一种嗜中性粒细胞结合的第二荧光标记抗体（第二抗体），和（c）第三荧光 标记的抗体（第3抗体），其与至少一种未成熟的粒细胞细胞结合，以染色样品中的白细胞，并从样品中除去红细胞; （2）使用流式细胞仪分析所得样品以测量至少一个散射光信号和三个分离的荧光信号; （3）基于散射光的强度和第一抗体的荧光强度来定义一组粒细胞; （4）基于来自第一抗体的荧光强度和来自第二或第三抗体的荧光强度来定义所定义的颗粒细胞组中的嗜中性细胞; （5）基于来自第二抗体的荧光强度和来自第三抗体的荧光强度，将所定义的嗜中性粒细胞群分类成不同程度的嗜中性粒细胞组，并计数第 每个组中的细胞。

    Apparatus and method for displaying normalized clinical test data
    6.
    发明授权
    Apparatus and method for displaying normalized clinical test data 失效
    用于显示标准化临床测试数据的装置和方法

    公开(公告)号：US5675760A

    公开(公告)日：1997-10-07

    申请号：US303205

    申请日：1994-09-08

    申请人： Berend Houwen ,  Shigeo Kanamori ,  Kaoru Asano

    发明人： Berend Houwen ,  Shigeo Kanamori ,  Kaoru Asano

    IPC分类号： G06Q50/22 ,  G06F19/00 ,  G06T11/00

    CPC分类号： G06F19/3487 ,  G01N2035/00891 ,  G06F19/3406 ,  G06F19/345

    摘要： A calculator selects desired data out of a set of data obtained by analyzing a sample, such as blood or urine, and normalizes the selected data with respect to a predetermined level. The normalized values obtained by the calculator may be displayed as values and/or graphs. The graphical display may show a partition line set according to the experiences of the laboratory, so the graph may be quickly understood.

    摘要翻译： 计算器通过分析诸如血液或尿液的样品而获得的一组数据中的所需数据，并相对于预定水平对所选数据进行归一化。 由计算器获得的归一化值可以显示为值和/或图。 图形显示可以根据实验室的经验显示分割线集合，因此可以快速了解图形。