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29 条记录 (耗时 0.022 秒)

    Application of fluorescent protein to garden plant
    1.
    发明授权
    Application of fluorescent protein to garden plant 有权
    荧光蛋白在花园植物中的应用

    公开(公告)号：US08203032B2

    公开(公告)日：2012-06-19

    申请号：US12374995

    申请日：2007-07-25

    申请人： Iwao Waga ,  Hiromi Takenaka ,  Shu Muto

    发明人： Iwao Waga ,  Hiromi Takenaka ,  Shu Muto

    IPC分类号： C12N15/82 ,  C12N15/84 ,  C12N15/12

    CPC分类号： C12N15/8212 ,  C07K14/43509

    摘要： The present invention provides a process for generation of a transformed plant capable of emitting fluorescence by introducing a gene encoding a non-plant-derived fluorescent protein into a plant such that the fluorescent protein is recombinantly expressed in the active form of its mature protein in the leaf or petal of the plant, and also provides a transformed garden plant capable of emitting fluorescence that is generated by using the process. For example, cDNA encoding the full-length amino acid sequence of a Chiridius poppei-derived fluorescent protein CpYGFP or its H52F modified protein CpYGFP H52F is inserted into a T-DNA-based expression vector system, which is in turn introduced into the chromosomal DNA of a plant. As a result, the transformed plant thus generated can exhibit fluorescence attributed to these fluorescent proteins and exhibit no substantial difference in the other phenotypes from wild-type one of the plant.

    摘要翻译： 本发明提供一种通过将编码非植物来源的荧光蛋白的基因导入植物而产生能够发射荧光的转化植物的方法，使得荧光蛋白以其成熟蛋白的活性形式重组表达 植物的叶或花瓣，并且还提供能够发射通过使用该过程产生的荧光的转化的花园植物。 例如，将编码Chiridius Poppei衍生的荧光蛋白CpYGFP或其H52F修饰的蛋白质CpYGFP H52F的全长氨基酸序列的cDNA插入到基于T-DNA的表达载体系统中，其进而导入染色体DNA 的植物。 结果，由此产生的转化植物可以表现出归因于这些荧光蛋白的荧光，并且在野生型植物中的其它表型中没有显示实质性差异。

    APPLICATION OF FLUORESCENT PROTEIN TO GARDEN PLANT
    2.
    发明申请
    APPLICATION OF FLUORESCENT PROTEIN TO GARDEN PLANT 有权
    荧光蛋白应用于园艺植物

    公开(公告)号：US20100043104A1

    公开(公告)日：2010-02-18

    申请号：US12374995

    申请日：2007-07-25

    申请人： Iwao Waga ,  Hiromi Takenaka ,  Shu Muto

    发明人： Iwao Waga ,  Hiromi Takenaka ,  Shu Muto

    IPC分类号： C12N15/82

    CPC分类号： C12N15/8212 ,  C07K14/43509

    摘要： The present invention provides a process for generation of a transformed plant capable of emitting fluorescence by introducing a gene encoding a non-plant-derived fluorescent protein into a plant such that the fluorescent protein is recombinantly expressed in the active form of its mature protein in the leaf or petal of the plant, and also provides a transformed garden plant capable of emitting fluorescence that is generated by using the process. For example, cDNA encoding the full-length amino acid sequence of a Chiridius poppei-derived fluorescent protein CpYGFP or its H52F modified protein CpYGFP H52F is inserted into a T-DNA-based expression vector system, which is in turn introduced into the chromosomal DNA of a plant. As a result, the transformed plant thus generated can exhibit fluorescence attributed to these fluorescent proteins and exhibit no substantial difference in the other phenotypes from wild-type one of the plant.

    摘要翻译： 本发明提供一种通过将编码非植物来源的荧光蛋白的基因导入植物而产生能够发射荧光的转化植物的方法，使得荧光蛋白以其成熟蛋白的活性形式重组表达 植物的叶或花瓣，并且还提供能够发射通过使用该过程产生的荧光的转化的花园植物。 例如，将编码Chiridius Poppei衍生的荧光蛋白CpYGFP或其H52F修饰的蛋白质CpYGFP H52F的全长氨基酸序列的cDNA插入到基于T-DNA的表达载体系统中，其进而导入染色体DNA 的植物。 结果，由此产生的转化植物可以表现出归因于这些荧光蛋白的荧光，并且在野生型植物中的其它表型中没有显示实质性差异。

    Nucleic acid molecule capable of binding to c-Met and use thereof
    8.
    发明授权
    Nucleic acid molecule capable of binding to c-Met and use thereof 有权
    能够结合c-Met的核酸分子及其用途

    公开(公告)号：US08822667B2

    公开(公告)日：2014-09-02

    申请号：US13812190

    申请日：2011-07-26

    申请人： Naomi Hirabayashi ,  Shotaro Tsuji ,  Jou Akitomi ,  Shintarou Katou ,  Iwao Waga ,  Takashi Ohtsu

    发明人： Naomi Hirabayashi ,  Shotaro Tsuji ,  Jou Akitomi ,  Shintarou Katou ,  Iwao Waga ,  Takashi Ohtsu

    IPC分类号： C07H21/04 ,  C07H21/02 ,  A61K48/00

    CPC分类号： C07H21/02 ,  A61K31/52 ,  A61K31/7105 ,  C12N15/115 ,  C12N2310/16 ,  C12Q1/6883 ,  C12Q2525/301 ,  C12Q2527/125 ,  A61K2300/00

    摘要： The present invention provides a nucleic acid molecule capable of binding to c-Met as a substance that can be used for clarification of the pathogenic mechanism of diseases caused by c-Met, diagnosis and treatment of the diseases, and the like, and also the use thereof. The c-Met binding nucleic acid molecule of the present invention is any one of the following nucleic acid molecules (A1), (A2), (B1), and (B2). (A1) a nucleic acid molecule including the base sequence of any one of SEQ ID NOs: 1 to 38 (A2) a nucleic acid molecule that is capable of binding to c-Met and includes a base sequence obtained by substitution, deletion, addition, and/or insertion of one or more bases in the base sequence of any one of SEQ ID NOs: 1 to 38 (B1) a nucleic acid molecule including the base sequence of any one of SEQ ID NOs: 39 to 76 (B2) a nucleic acid molecule that is capable of binding to c-Met and includes a base sequence obtained by substitution, deletion, addition, and/or insertion of one or more bases in the base sequence of any one of SEQ ID NOs: 39 to 76.

    摘要翻译： 本发明提供能够结合c-Met的核酸分子，作为能够用于澄清由c-Met，疾病的诊断和治疗等引起的疾病的致病机制的物质，以及 使用它。 本发明的c-Met结合核酸分子是以下核酸分子（A1），（A2），（B1）和（B2）中的任一种。 （A1）包含SEQ ID NO：1至38（A2）中任一个的碱基序列的核酸分子，其能够结合c-Met并包含通过取代，缺失，加成获得的碱基序列 ，（SEQ ID NO：39）至（38）中的任何一个的碱基序列的核酸分子，和/或在SEQ ID NO：1至38（B1）中任一个的碱基序列中插入一个或多个碱基， 能够结合c-Met的核酸分子，并且包含通过SEQ ID NO：39至76中任一个的碱基序列中的一个或多个碱基的取代，缺失，添加和/或插入获得的碱基序列 。

    Prediction device, prediction method, program, and recording medium
    9.
    发明授权
    Prediction device, prediction method, program, and recording medium 有权
    预测装置，预测方法，程序和记录介质

    公开(公告)号：US09454642B2

    公开(公告)日：2016-09-27

    申请号：US13807876

    申请日：2011-07-02

    申请人： Jou Akitomi ,  Shintarou Katou ,  Shotaro Tsuji ,  Iwao Waga

    发明人： Jou Akitomi ,  Shintarou Katou ,  Shotaro Tsuji ,  Takashi Ohtsu ,  Iwao Waga

    IPC分类号： G01N33/50 ,  G06F19/16 ,  C12N15/115 ,  G06F19/18

    CPC分类号： G06F19/16 ,  C12N15/115 ,  C12N2310/16 ,  G06F19/18

    摘要： The present invention provides a prediction device, a prediction method, a program, and a recording medium, with which whether or not desired aptamer sequences are enriched can be predicted easily. The prediction device of the present invention 10 includes an input unit 11, a calculation unit 12, and a prediction unit 13. The input unit 11 is a unit through which sequence information on a target aptamer sequence group including selected aptamers in a target pool and a reference aptamer sequence group including reference aptamer sequences are inputted. The calculation unit 12 calculates the free energy of the target aptamer sequence group and the free energy of the reference aptamer sequence group. The prediction unit 13 compares the free energy of these sequence groups, and predicts that the target pool is an enriched pool when the free energy of the target aptamer sequence group is lower than the free energy of the reference aptamer sequence group. The reference aptamer sequence group is a candidate aptamer sequence group including a plurality of candidate aptamer sequences or a virtual aptamer sequence group that is derived from the target aptamer sequence group and includes virtual aptamer sequences having the same base composition as the target aptamer sequence group.

    摘要翻译： 本发明提供一种预测装置，预测方法，程序和记录介质，可以容易地预测其中是否需要富集需要的适体序列。 本发明的预测装置10包括输入单元11，计算单元12和预测单元13.输入单元11是通过目标池中包括所选择的适配体的目标适体序列组的序列信息和 输入包括参考适体序列的参照适体序列组。 计算单元12计算目标适体序列组的自由能和参考适体序列组的自由能。 预测单元13比较这些序列组的自由能，并且当靶适体序列组的自由能低于参考适体序列组的自由能时，预测目标池是富集池。 参照适体序列组是包含从目标适体序列组得到的多个候选适体序列或虚拟适体序列组的候选适体序列组，并且具有与靶适体序列组相同的基本组成的虚拟适配子序列。

    METHOD FOR EVALUATING REDOX ACTIVITY OF NUCLEIC ACID MOLECULE AND NUCLEIC ACID MOLECULE HAVING REDOX ACTIVITY
    10.
    发明申请
    METHOD FOR EVALUATING REDOX ACTIVITY OF NUCLEIC ACID MOLECULE AND NUCLEIC ACID MOLECULE HAVING REDOX ACTIVITY 有权
    用于评估具有还原活性的核酸分子和核酸分子的还原活性的方法

    公开(公告)号：US20140128589A1

    公开(公告)日：2014-05-08

    申请号：US14129392

    申请日：2012-07-02

    申请人： Naoto Kaneko ,  Katsunori Horii ,  Jou Akitomi ,  Shintarou Katou ,  Iwao Waga

    发明人： Naoto Kaneko ,  Katsunori Horii ,  Jou Akitomi ,  Shintarou Katou ,  Iwao Waga

    IPC分类号： C12N15/113 ,  G01N27/26 ,  G01N33/58

    CPC分类号： C12N15/113 ,  C12N15/1034 ,  C12N15/111 ,  C12N15/115 ,  C12N2310/127 ,  C12N2310/16 ,  C12N2310/351 ,  C12N2320/10 ,  C12N2330/31 ,  C12Q1/26 ,  C12Q1/6825 ,  G01N27/26 ,  G01N33/581 ,  C12Q2304/80 ,  C12Q2525/205 ,  C12Q2563/113

    摘要： The present invention provides a novel technique by which the redox activity of a nucleic acid molecule can be evaluated. An evaluation method of the present invention includes: a detection step of electrochemically detecting a redox reaction to a substrate, the redox reaction being catalyzed by a nucleic acid molecule to be evaluated, using a device that electrochemically detects a redox reaction; and an evaluation step of evaluating redox activity of the nucleic acid molecule from a result of the detection of the redox reaction. As the device, a device in which a base provided with a detection portion is included, the detection portion.includes an electrode system, and the nucleic acid molecule to be evaluated is arranged on the base is used. In the present invention, it is preferred that a plurality of kinds of nucleic acid molecule to be evaluated is arranged on the base, and the plurality of kinds of nucleic acid molecules to be evaluated is evaluated by a single device.

    摘要翻译： 本发明提供可以评价核酸分子的氧化还原活性的新技术。 本发明的评价方法包括：使用电化学检测氧化还原反应的装置电化学检测对基底的氧化还原反应的检测步骤，所述氧化还原反应由待评价的核酸分子催化; 以及从检测氧化还原反应的结果来评价核酸分子的氧化还原活性的评价步骤。 作为该装置，包括具有检测部的基部的检测部。 包括电极系统，并且使用要评估的核酸分子设置在基底上。 在本发明中，优选在基材上排列要评价的多种核酸分子，通过单个装置评价要评价的多种核酸分子。