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    • 1. 发明授权
    • Degree of hybridization detection method
    • 杂交检测方法
    • US06775621B1
    • 2004-08-10
    • US09459712
    • 1999-12-13
    • Noriko YurinoKenji YamamotoToshiaki ItoToshimasa Watanabe
    • Noriko YurinoKenji YamamotoToshiaki ItoToshimasa Watanabe
    • G01N3348
    • C12Q1/6837C12Q2545/114C12Q2545/101C12Q2563/107C12Q2565/102
    • The present invention provides a hybridization detection method capable of quantitatively determining the degree of the hybridization between a sample biopolymer and a probe biopolymer. In the method, the amount of a fluorescently labeled probe immobilized on a substrate as a spot is quantitatively determined by determining the fluorescence emitted from a fluorescent material labeling the probe, and the amount of a fluorescently labeled sample hybridized to the probe is quantitatively determined by determining the fluorescence emitted from the fluorescent material labeling the sample. The difference between the amount of the probe and the amount of the sample is normalized with the amount of the probe. Based on the normalized value, the amount of the sample hybridized to the probe can be determined relative to the amount of the probe spotted on the substrate.
    • 本发明提供能够定量测定样品生物聚合物和探针生物聚合物之间的杂交程度的杂交检测方法。 在该方法中,通过测定从标记探针的荧光物质发出的荧光来定量测定固定在基板上的荧光标记探针作为斑点的量,并且通过用探针杂交的荧光标记的样品的量定量地测定 确定从标记样品的荧光材料发出的荧光。 探针的量与样品量之间的差异用探针的量进行归一化。 基于归一化值,可以相对于在基板上点样的探针的量来确定与探针杂交的样品的量。
    • 2. 发明授权
    • Device for electrophoresis
    • 电泳装置
    • US06755952B1
    • 2004-06-29
    • US09787128
    • 2001-03-13
    • Kenji YamamotoNoriko Yurino
    • Kenji YamamotoNoriko Yurino
    • G01N27453
    • G01N27/44791G01N27/44721
    • The present invention allows detection in short time while maintaining the level of the resolving power as high as when a capillary is utilized. The entire surface of an electrophoresis board 10, which is provided with a two-dimensional tubular electrophoresis pathway, is irradiated with excitation light so as to pick up fluorescence or luminescence from a sample with a two-dimensional sensor. By reading the entire electrophoresis pathway, the separated state of the sample may be confirmed during the electrophoresis. As a result, the electrophoresis may be ended when the sample is sufficiently separated and a molecular weight thereof may be determined based on the migration distance.
    • 本发明允许在短时间内进行检测,同时保持分辨能力的水平高达使用毛细管时的高度。设置有二维管状电泳通路的电泳板10的整个表面用激发 以便从具有二维传感器的样品中吸收荧光或发光。 通过读取整个电泳途径,可以在电泳期间确认样品的分离状态。 结果,当样品充分分离并且可以基于迁移距离确定分子量时,可以结束电泳。