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MEASUREMENT METHOD OF PERIPHERAL BLOOD NEUTROPHIL APOPTOSIS

机译:外周血中性神经细胞凋亡的测定方法

摘要

PROBLEM TO BE SOLVED: To provide methods of measuring the ratio of peripheral blood neutrophil apoptosis, in which the ratio of in vivo neutrophil apoptosis is grasped rapidly and simply in real time, while minimizing the effect on the neutrophil after blood collecting.;SOLUTION: A method of measuring the ratio of peripheral blood neutrophil apoptosis comprises (a) a step in which neutrophils are separated from a biogenic blood sample and washed with phosphate buffered saline (PBS) to prepare a neutrophil suspension (phosphate buffered saline) with a concentration of 1×107/mL or more; (b) mixing the neutrophil suspension with the apoptosis Dye and subsequently culturing; (c) examining the cultured neutrophil suspension with a microscope using a hemocytometer and counting the ratio of dyed apoptosis positive neutrophils to the total count of the neutrophils in one visual field, wherein the centrifugation is performed for 3 to 10 minutes at 400 to 800 g, the concentration of the apoptosis Dye is 2 to 5%, and the culture is performed in 5% carbonic acid gas at 37°C for 8 to 10 minutes.;SELECTED DRAWING: Figure 3;COPYRIGHT: (C)2017,JPO&INPIT
机译:要解决的问题:提供一种测量外周血中性粒细胞凋亡率的方法,其中可以快速,简单地实时掌握体内中性粒细胞凋亡率,同时将采血后对中性粒细胞的影响降至最低。解决方案:一种测量外周血中性粒细胞凋亡比率的方法,其包括:(a)从生物血样中分离中性粒细胞,并用磷酸盐缓冲盐水(PBS)洗涤,以制备浓度为0.1μg的中性粒细胞悬液(磷酸盐缓冲盐水)的步骤。 1×10 7 / mL或更高; (b)将中性粒细胞悬浮液与细胞凋亡染料混合,然后培养; (c)使用血球计数器在显微镜下检查培养的嗜中性粒细胞悬液,并在一个视野中计数染色的凋亡阳性嗜中性粒细胞与嗜中性粒细胞总数的比率,其中在400至800g下离心3至10分钟,凋亡染料的浓度为2%到5%,并在5%的碳酸气体中于37°C进行培养8到10分钟。;部分附图:图3;版权:(C)2017,JPO&INPIT

著录项

  • 公开/公告号JP2017108660A

    专利类型

  • 公开/公告日2017-06-22

    原文格式PDF

  • 申请/专利权人 HANUMAT CO LTD;

    申请/专利号JP20150244235

  • 发明设计人 TANAKA KOJI;KUSUNOKI MASATO;

    申请日2015-12-15

  • 分类号C12Q1/02;G01N33/48;

  • 国家 JP

  • 入库时间 2022-08-21 13:59:56

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