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    • 2. 发明授权
    • Nucleic acid base pair
    • 核酸碱基对
    • US07667031B2
    • 2010-02-23
    • US11078607
    • 2005-03-10
    • Ichiro HiraoMasahide IshikawaTsuyoshi FujiharaShigeyuki Yokoyama
    • Ichiro HiraoMasahide IshikawaTsuyoshi FujiharaShigeyuki Yokoyama
    • C07H21/00C07H21/04C07H19/06C07H19/048
    • C07H11/04C07H19/207C07H21/00C12N15/11C12P21/02
    • A novel artificial nucleic acid base pair which is obtained by forming a selective base pair by introducing a group having steric hindrance (preferably a group having steric hindrance and static repulsion and a stacking effect) and can be recognized by a polymerase such as DNA polymerase; a novel artificial gene; and a method of designing nucleic acid bases so as to form a selective base pair with the use of steric hindrance, static repulsion and stacking effect at the base moiety of the nucleic acid. An artificial nucleic acid comprising these bases; a process for producing the same; a codon containing the same; a nucleic acid molecule containing the same; a process for producing a non-natural gene by using the same; a process for producing a novel protein by using the above nucleic acid molecule or non-natural gene, and the like.
    • 通过引入具有空间位阻的基团(优选具有空间位阻和静电排斥和堆叠效应的基团)形成选择性碱基对而获得的新型人造核酸碱基对,可以通过聚合酶如DNA聚合酶识别; 一种新型人工基因; 以及设计核酸碱基以在核酸的碱基部分上使用空间位阻,静电排斥和堆叠效应形成选择性碱基对的方法。 包含这些碱的人造核酸; 其制造方法; 含有相同的密码子; 含有该核酸分子的核酸分子; 通过使用该方法生产非天然基因的方法; 通过使用上述核酸分子或非天然基因来生产新型蛋白质的方法等。
    • 4. 发明授权
    • Nucleic acid base pair
    • 核酸碱基对
    • US07101992B1
    • 2006-09-05
    • US09787196
    • 2000-07-14
    • Ichiro HiraoMasahide IshikawaTsuyoshi FujiharaShigeyuki Yokoyama
    • Ichiro HiraoMasahide IshikawaTsuyoshi FujiharaShigeyuki Yokoyama
    • C07H21/00C07H19/16C07H19/048
    • C07H11/04C07H19/207C07H21/00C12N15/11C12P21/02
    • A novel artificial nucleic acid base pair which is obtained by forming a selective base pair by introducing a group having steric hindrance (preferably a group having steric hindrance and static repulsion and a stacking effect) and can be recognized by a polymerase such as DNA polymerase; a novel artificial gene; and a method of designing nucleic acid bases so as to form a selective base pair with the use of steric hindrance, static repulsion and stacking effect at the base moity of the nucleic acid. An artificial nucleic acid comprising these bases; a process for producing the same; a codon containing the same; a nucleic acid molecule containing the same; a process for producing a non-natural gene by using the same; a process for producing a novel protein by using the above nucleic acid molecule or non-natural gene, and the like.
    • 通过引入具有空间位阻的基团(优选具有空间位阻和静电排斥和堆叠效应的基团)形成选择性碱基对而获得的新型人造核酸碱基对,可以通过聚合酶如DNA聚合酶识别; 一种新型人工基因; 以及设计核酸碱基的方法,以便在核酸的基础上使用空间位阻,静电排斥和堆叠效应形成选择性碱基对。 包含这些碱的人造核酸; 其制造方法; 含有相同的密码子; 含有该核酸分子的核酸分子; 通过使用该方法生产非天然基因的方法; 通过使用上述核酸分子或非天然基因来生产新型蛋白质的方法等。
    • 7. 发明申请
    • Protein detecting device
    • 蛋白检测装置
    • US20100144060A1
    • 2010-06-10
    • US12654137
    • 2009-12-11
    • Shozo FujitaShunsaku TakeishiTsuyoshi Fujihara
    • Shozo FujitaShunsaku TakeishiTsuyoshi Fujihara
    • G01N33/543
    • G01N33/5438G01N33/53G01N33/542G01N33/54353G01N33/68
    • A protein detecting device, which comprises: (1) a detecting unit having a bonding section, which has properties for specifically bonding to a protein to be detected, a detecting section for detecting the bonding of the protein to be detected to the bonding section, the detecting section being made up of a polynucleotide double strand and a charge separating group, and an electrode section detecting the change in electrical conductivity of, or amount of transferred charge in, the polynucleotide double strand modified by the bond of the protein, (2) a standard electrode, (3) a reference electrode, (4) a container for housing the detecting unit, the standard electrode and the reference electrode, and containing a sample solutions comprising the protein to be detected, and (5) a measuring unit for measuring the protein based on a signal detected in the detecting unit.
    • 一种蛋白质检测装置,其特征在于,包括:(1)检测单元,具有具有特异性地结合待检测蛋白质的接合部的检测部,检测所述被检测蛋白质与接合部的接合的检测部, 检测部分由多核苷酸双链和电荷分离基团组成,电极部分检测由蛋白质键修饰的多核苷酸双链中的导电性或转移电荷量的变化(2 )标准电极,(3)参考电极,(4)容纳检测单元,标准电极和参比电极的容器,并包含含有待检测蛋白质的样品溶液,和(5)测量单元 用于基于在检测单元中检测到的信号测量蛋白质。
    • 8. 发明授权
    • Functional molecule and process for producing the same
    • 功能分子及其制备方法
    • US07517646B2
    • 2009-04-14
    • US10943150
    • 2004-09-17
    • Tsuyoshi FujiharaShozo FujitaShunsaku Takeishi
    • Tsuyoshi FujiharaShozo FujitaShunsaku Takeishi
    • C12Q1/68C12P19/34C07H21/00C07H21/02C07H19/04
    • A61K31/7115A61K48/00C07H21/00C12N15/1048C12N15/1058C12N15/115C12N2310/53
    • A process for producing a functional molecule includes a forming step which forms a modified nucleotide n-mer (where, n represents an integer) containing a modified nucleoside prepared by introducing a substituent into a nucleoside composing a nucleic acid; and a producing step which produces a modified oligonucleotide sequence by randomly polymerizing the modified nucleotide n-mer. A preferable embodiment thereof includes a selecting step which selects a sequence having an affinity to a target from the modified oligonucleotide sequence, a determining step which amplifies the selected modified oligonucleotide sequence and determines the base sequence thereof, and a translating step which translates the sequence of the modified oligonucleotide sequence on the basis of a relation table prepared by relating at least one of 4n kinds of nucleotide n-mers, which are presented in the relation table prepared by the one-to-one combination of 4 kinds of nucleosides, to a modified nucleotide n-mer.
    • 制备功能性分子的方法包括:形成步骤,其形成含有通过将取代基引入构成核酸的核苷中制备的修饰核苷的修饰的核苷酸n-mer(其中,n表示整数); 以及通过随机聚合修饰的核苷酸n-mer产生修饰的寡核苷酸序列的制备步骤。 其优选实施方案包括从修饰的寡核苷酸序列中选择与靶具有亲和性的序列的选择步骤,放大所选择的修饰寡核苷酸序列并确定其碱基序列的确定步骤,以及翻译步骤, 基于通过将通过将4种核苷的一对一组合制备的关系表中存在的4n种核苷酸n-mers中的至少一种与至少一种核苷酸n-mers相关联的关系表,修饰的寡核苷酸序列与 修饰的核苷酸n-mer。