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    • 4. 发明授权
    • Method of analyzing physiological function of target substance
    • 分析目标物质生理功能的方法
    • US07553624B2
    • 2009-06-30
    • US10557906
    • 2004-05-20
    • Takeharu NagaiAtsushi Miyawaki
    • Takeharu NagaiAtsushi Miyawaki
    • C12Q1/68C12Q1/70G01N33/53C07H19/04C07H21/02
    • G01N33/533
    • The present invention provides a method of analyzing the physiological function of a target substance by inactivating the physiological function of the target substance, comprising the steps of: (a) binding to the target substance a photoactive compound represented by formula (I): (in the formula, Q is a group for binding this compound with the target substance) to form a composite comprising the target substance and the photoactive compound; and (b) irradiating the obtained composite with light to inactivate the function of the target substance to which the photoactive compound has been bound, or to inactivate the function of the target substance at the site where the photoactive compound has been bound.
    • 本发明提供了通过使目标物质的生理功能失活来分析目标物质的生理功能的方法,包括以下步骤:(a)与目标物质结合由式(I)表示的光活性化合物:(在 式中,Q为与化合物与目标物质结合的基团),形成包含目标物质和光活性化合物的复合体; 和(b)用光照射得到的复合物,使光活性化合物结合的目标物质的功能失活,或者使光活性化合物结合的位置失活目标物质的功能。
    • 6. 发明申请
    • FLUORESCENT PROTEIN
    • 荧光蛋白
    • US20080166799A1
    • 2008-07-10
    • US11739133
    • 2007-04-24
    • Atsushi MIYAWAKISatoshi KARASAWA
    • Atsushi MIYAWAKISatoshi KARASAWA
    • C12N5/06C07H21/04C12N15/63
    • C07K14/37
    • An object of the present invention is to provide a novel fluorescent protein derived from organisms other than Aequorea victoria. According to the present invention, there is provided a fluorescent protein derived from Fungia sp., which has the following properties: (1) the excitation maximum wavelength is 455 nm, and the fluorescence maximum wavelength is 488 nm; (2) the molar absorption coefficient at 455 nm is 38700 or 27700; (3) the quantum yield is 0.85 or 0.81; and (4) the pH sensitivity of the fluorescent property is stable at pH 5 to 9; and a fluorescent protein derived from Fungia sp., which has the following properties: (1) the excitation maximum wavelength is 548 nm, and the fluorescence maximum wavelength is 561 nm; (2) the molar absorption coefficient at 548 nm is 75900 or 51000; (3) the quantum yield is 0.44 or 0.50; and (4) the pH sensitivity of the fluorescent property is pKa
    • 本发明的目的是提供一种源自维他命A(Aequorea victoria)以外的生物体的新型荧光蛋白。 根据本发明,提供了一种衍生自真菌属的荧光蛋白,具有以下性质:(1)激发最大波长为455nm,荧光最大波长为488nm; (2)455nm处的摩尔吸光系数为38700或27700; (3)量子产率为0.85或0.81; 和(4)荧光性能的pH敏感性在pH5至9下是稳定的; 和一种来自真菌属的荧光蛋白,具有以下特性:(1)激发最大波长为548nm,荧光最大波长为561nm; (2)548nm处的摩尔吸光系数为75900或51000; (3)量子产率为0.44或0.50; 和(4)荧光性质的pH敏感度为pKa <5.0。
    • 7. 发明申请
    • Method of detecting micronucleus in cell
    • 检测细胞中微核的方法
    • US20070207452A1
    • 2007-09-06
    • US11729529
    • 2007-03-29
    • Hirobumi SuzukiAtsushi Miyawaki
    • Hirobumi SuzukiAtsushi Miyawaki
    • C12Q1/00C12Q1/68
    • G01N33/5017
    • The present invention provides a method of detecting a micronucleus in a living cell to be measured, without having to fixate the cell, characterized by comprising generating a mother cell by introducing a gene encoding a single or a plurality of nucleus-related proteins and a gene encoding a fluorescence protein into a culture cell, and making then expressed in the cell, subjecting the cell to a treatment for a toxicity test or a mutagenicity test of a test substance, performing a limited excitation which makes a region of the micronucleus emit fluorescence limitedly, and quantitatively measuring an amount of the fluorescence corresponding to a component of the nucleus-related protein.
    • 本发明提供一种检测待测细胞中的微核的方法,而不必固定细胞,其特征在于包括通过引入编码单个或多个核相关蛋白的基因和基因产生母细胞 将荧光蛋白编码到培养细胞中,然后在细胞中表达,对细胞进行毒性试验或试验物质的诱变试验处理,进行有限激发,使微核区域有限地发射荧光 并定量测定与核相关蛋白质的成分相对应的荧光量。