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    • 2. 发明授权
    • Apparatus for microinjection of sample into amphibian oocytes
    • 用于将样品显微注射到两栖动物卵母细胞中的装置
    • US06593129B1
    • 2003-07-15
    • US09666530
    • 2000-09-20
    • Tomoko TakeshitaJun OtomoSayuri NomuraShokichi MatsunamiNoboru MoriyaSakae Saito
    • Tomoko TakeshitaJun OtomoSayuri NomuraShokichi MatsunamiNoboru MoriyaSakae Saito
    • C12M100
    • C12M23/50C12M35/00
    • An apparatus for microinjection of samples into amphibian oocytes, comprising a tray for holding a plurality of the amphibian oocytes, an injection needle for injecting a sample into the said amphibian oocytes, a driving means for moving a relative position between the said tray and the said injection needle and a controlling means for controlling the said movement by imputing a depth of the said injection needle for the said tray or the said amphibian oocytes in the injection of the sample, and injecting the sample into the said amphibian oocytes at the said depth. According to the present invention, the sample can be injected into the amphibian oocyte with constant depth.precisely and quality of oocyte or a positional site of needle injection can be recorded as the information.
    • 一种用于将样品显微注射到两栖动物卵母细胞中的装置,包括用于保持多个两栖动物卵母细胞的托盘,用于将样品注入所述两栖动物卵母细胞的注射针;驱动装置,用于使所述托盘和所述 注射针和控制装置,用于通过在注射样品时插入所述托盘或所述两栖动物卵母细胞的所述注射针的深度来控制所述运动,以及在所述深度将样品注入所述两栖动物卵母细胞。 根据本发明,可以将样品以恒定的深度精确地注入到两栖动物卵母细胞中,并且可以记录卵母细胞的质量或针注射的位置位置作为信息。
    • 7. 发明授权
    • Histamine measuring apparatus and a histamine measuring method
    • 组胺测定装置和组胺测定方法
    • US06337178B2
    • 2002-01-08
    • US09843866
    • 2001-04-30
    • Tomoko TakeshitaJun Otomo
    • Tomoko TakeshitaJun Otomo
    • C12M300
    • G01F1/00G01N2333/726Y10S435/808Y10S436/805Y10S436/806Y10S436/807Y10S436/826Y10T436/108331
    • Histamine may be quantitatively measured by performing the following steps. First, an oocyte that expresses histamine receptors is held in a recess formed at the bottom of a vessel. Then, first and second electrodes are inserted into the oocyte. Subsequently, the membrane potential of the oocyte is measured by using the first electrode to stabilize this membrane potential at a predetermined level by driving a current through the second electrode using circuitry for clamping the membrane potential of the oocyte. A sample is then infused into a fine reacting tube having an antigen immobilized on its inner surface together with some buffer solution to promote a histamine releasing reaction. The solution containing histamines that is released in the fine reacting tube is transferred to the vessel to make contact with the oocyte in the vessel. Finally, an electric response of the oocyte caused by the contact with the solution is detected and the concentration of the histamine released in the histamine releasing reaction in the fine reacting tube is determined. The entire blood or mast cell suspension may be used as a sample without pretreatment.
    • 组胺可以通过以下步骤进行定量测定。 首先,表达组胺受体的卵母细胞被保持在形成于血管底部的凹陷中。 然后,将第一和第二电极插入卵母细胞。 随后,通过使用第一电极通过使用用于钳位卵母细胞的膜电位的电路驱动通过第二电极的电流来将该膜电位稳定在预定水平来测量卵母细胞的膜电位。 然后将样品输入到具有固定在其内表面上的抗原与一些缓冲溶液的细小反应管中,以促进组胺释放反应。 将包含在细反应管中释放的组胺的溶液转移到容器中以与容器中的卵母细胞接触。 最后,检测由与溶液接触引起的卵母细胞的电响应,并确定微反应管中组胺释放反应中释放的组胺浓度。 整个血液或肥大细胞悬浮液可以用作样品而不进行预处理。
    • 9. 发明授权
    • Histamine measuring apparatus and a histamine measuring method
    • US06277559B1
    • 2001-08-21
    • US09788361
    • 2001-02-21
    • Tomoko TakeshitaJun Otomo
    • Tomoko TakeshitaJun Otomo
    • C12Q100
    • Histamine may be quantitatively measured by performing the following steps. First, an oocyte that expresses histamine receptors is held in a recess formed at the bottom of a vessel. Then, first and second electrodes are inserted into the oocyte. Subsequently, the membrane potential of the oocyte is measured by using the first electrode to stabilize this membrane potential at a predetermined level by driving a current through the second electrode using circuitry for clamping the membrane potential of the oocyte. A sample is then infused into a fine reacting tube having an antigen immobilized on its inner surface together with some buffer solution to promote a histamine releasing reaction. The solution containing histamines that is released in the fine reacting tube is transferred to the vessel to make contact with the oocyte in the vessel. Finally, an electric response of the oocyte caused by the contact with the solution is detected and the concentration of the histamine released in the histamine releasing reaction in the fine reacting tube is determined. The entire blood or mast cell suspension may be used as a sample without pretreatment.