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    • 5. 发明授权
    • Capillary electrophoresis apparatus
    • 毛细管电泳仪
    • US08702949B2
    • 2014-04-22
    • US13263040
    • 2010-04-08
    • Takeshi OhuraRyoji InabaManabu AkibaTakashi GomiMari Kotoura
    • Takeshi OhuraRyoji InabaManabu AkibaTakashi GomiMari Kotoura
    • G01N27/453
    • G01N27/44743G01N27/44782
    • The solution reservoir apparatus of the capillary electrophoresis apparatus securely affixes an evaporation-preventing membrane to a container when a capillary is inserted or withdrawn, without extending the cathode end of the capillary. The solution reservoir apparatus comprises a container for reserving a sample or solution, a cover having a bore through which the capillary is passed and covering the container, an evaporation-preventing membrane having a capillary hole through which the capillary is passed, and a container holder for holding the container. The evaporation-preventing membrane has a projection provided at the periphery of the capillary hole, the projection of the evaporation-preventing membrane is engaged with the bore on the cover when the evaporation-preventing membrane is positioned on the cover, and the evaporation-preventing membrane is supported by the cover.
    • 当毛细管插入或取出时,毛细管电泳装置的溶液储存装置在不延长毛细管的阴极端的情况下,将防蒸发膜牢固地固定在容器上。 溶液储存装置包括用于储存样品或溶液的容器,具有孔的盖,毛细管穿过孔覆盖容器,具有毛细孔通过的毛细孔的防蒸发膜和容器保持架 用于拿着容器。 防蒸发膜具有设置在毛细孔周边的突起,当防蒸发膜位于盖上时,防蒸发膜的突起与盖上的孔接合,并且防蒸发膜 膜由盖支撑。
    • 6. 发明申请
    • CAPILLARY ELECTROPHORESIS APPARATUS
    • 毛细管电泳装置
    • US20120024707A1
    • 2012-02-02
    • US13263040
    • 2010-04-08
    • Takeshi OhuraRyoji InabaManabu AkibaTakashi GomiMari Kotoura
    • Takeshi OhuraRyoji InabaManabu AkibaTakashi GomiMari Kotoura
    • G01N27/453
    • G01N27/44743G01N27/44782
    • The solution reservoir apparatus of the capillary electrophoresis apparatus securely affixes an evaporation-preventing membrane to a container when a capillary is inserted or withdrawn, without extending the cathode end of the capillary. The solution reservoir apparatus comprises a container for reserving a sample or solution, a cover having a bore through which the capillary is passed and covering the container, an evaporation-preventing membrane having a capillary hole through which the capillary is passed, and a container holder for holding the container. The evaporation-preventing membrane has a projection provided at the periphery of the capillary hole, the projection of the evaporation-preventing membrane is engaged with the bore on the cover when the evaporation-preventing membrane is positioned on the cover, and the evaporation-preventing membrane is supported by the cover.
    • 当毛细管插入或取出时,毛细管电泳装置的溶液储存装置在不延长毛细管的阴极端的情况下,将防蒸发膜牢固地固定在容器上。 溶液储存装置包括用于储存样品或溶液的容器,具有孔的盖,毛细管穿过孔覆盖容器,具有毛细孔通过的毛细孔的防蒸发膜和容器保持架 用于拿着容器。 防蒸发膜具有设置在毛细孔周边的突起,当防蒸发膜位于盖上时,防蒸发膜的突起与盖上的孔接合,并且防蒸发膜 膜由盖支撑。
    • 7. 发明授权
    • Electrophoresis unit and electrophoretic analysis method
    • 电泳单元和电泳分析方法
    • US07943027B2
    • 2011-05-17
    • US11979570
    • 2007-11-06
    • Motohiro YamazakiRyoji InabaSatoshi TakahashiTomohiro ShojiTakeshi OhuraTakashi Gomi
    • Motohiro YamazakiRyoji InabaSatoshi TakahashiTomohiro ShojiTakeshi OhuraTakashi Gomi
    • G01N27/447G01N27/453
    • B01D57/02C07K1/26G01N27/44721G01N27/44782
    • The object of the present invention is that a dynamic range is extended in an electrophoresis unit and concentration differences among a plurality of samples measured simultaneously are increased.An irradiation time to the samples is adjusted during analysis without changing a sampling time. By shortening the irradiation time, a fluorescence amount of the samples is reduced to cause signal intensity detected by a detector to physically decrease. If the irradiation time is very short (several 100 msec), the irradiation time and fluorescence intensity are in a direct proportional relationship. It is known that, if the irradiation time is reduced to 1/n, the fluorescence intensity, that is, signal intensity to be detected will be 1/n. Thus, for data whose irradiation time is reduced to 1/n during analysis, data obtained by multiplying a substantially measured value by n is used for data analysis as a true value to be originally acquired.
    • 本发明的目的是在电泳单元中扩展动态范围,同时增加多个样本之间的浓度差。 在分析过程中调整样品的照射时间,而不改变采样时间。 通过缩短照射时间,减少样品的荧光量,使得由检测器检测出的信号强度物理降低。 如果照射时间非常短(几百毫秒),照射时间和荧光强度成正比关系。 已知如果照射时间减少到1 / n,则荧光强度即被检测信号强度为1 / n。 因此,对于在分析期间其照射时间减少到1 / n的数据,将通过将基本上测量的值乘以n获得的数据用作数据分析作为最初获取的真实值。