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    • 1. 发明申请
    • METHOD FOR SPECIFIC COVALENT COUPLING OF ANTIBODY USING A PHOTOACTIVABLE PROTEIN G VARIANT
    • 使用光化学蛋白G变体进行抗体的特异性共价连接的方法
    • WO2009136676A1
    • 2009-11-12
    • PCT/KR2008/002956
    • 2008-05-27
    • KOREA RESEARCH INSTITUTE OF BIOSCIENCE AND BIOTECHNOLOGYCHUNG, Bong HyunJUNG, Yong wonLEE, Jeong Min
    • CHUNG, Bong HyunJUNG, Yong wonLEE, Jeong Min
    • C07K14/315
    • C07K14/315G01N33/531G01N33/533
    • The present invention relates to a protein G variant comprising a mutated Fc binding domain, which is prepared by substituting cysteine for specific residues of the Fc-binding domain of protein G, and a method for preparing the same. Further, the present invention relates to a protein G variant comprising a cysteine mutated Fc binding domain that is site-selectively modified with a UV cross-linker. Further, the present invention relates to a method for UV cross-linking the protein G variant with antibody. The present invention relates to a protein G variant-antibody conjugate that is prepared by the above method. Further, the present invention provides a method for screening or analyzing antigens using the conjugate. Furthermore, the present invention provides a biochip or biosensor fabricated by linking the protein G variant to the surface of a solid support, and a method for fabricating the same. In addition, the present invention provides a method for immobilizing antibodies and analyzing antigens using the biochip or biosensor.
    • 本发明涉及包含通过用半胱氨酸代替蛋白G的Fc结合结构域的特异性残基制备的突变Fc结合结构域的蛋白G变体及其制备方法。 此外,本发明涉及包含用UV交联剂位点选择性修饰的半胱氨酸突变的Fc结合结构域的蛋白G变体。 此外,本发明涉及用抗体将蛋白G变体UV交联的方法。 本发明涉及通过上述方法制备的蛋白G变体 - 抗体缀合物。 此外,本发明提供了使用该缀合物筛选或分析抗原的方法。 此外,本发明提供通过将蛋白G变体与固体支持物的表面连接而制造的生物芯片或生物传感器及其制造方法。 此外,本发明提供了使用生物芯片或生物传感器固定抗体和分析抗原的方法。
    • 2. 发明申请
    • NOVEL RNA-BINDING PROTEIN AND LABEL-FREE DETECTION METHOD FOR DETECTING MICRORNA USING SAME
    • 新型RNA结合蛋白和用于检测MICRORNA的无标记检测方法
    • WO2012033382A3
    • 2012-06-28
    • PCT/KR2011006710
    • 2011-09-09
    • KOREA RES INST OF BIOSCIENCEJUNG YONG WONCHUNG BONG HYUNLEE JEONG MIN
    • JUNG YONG WONCHUNG BONG HYUNLEE JEONG MIN
    • C07K19/00C12N15/62C12Q1/68G01N33/68
    • C12Q1/6809C07K14/47C07K14/52C07K2319/00C12N9/22C12Q2522/101C12Q2525/207
    • The present invention relates to a novel RNA-binding protein, to a composition comprising same for detecting microRNA, and to a label-free detection method for detecting microRNA using same. According to the present invention, the method for detecting microRNA using the RNA-binding protein, which is a fusion protein comprising a PAZ domain and a double stranded RNA-binding domain and which binds to double stranded RNA having an overhanging 3' terminal, is a label-free detection method for detecting microRNA without an enzymatic labeling process or enzymatic amplifying reaction, which may overcome the drawbacks of conventional microRNA analysis methods, that is, methods for analyzing microRNA after enzymatic labeling or methods for coupling an antibody to microRNA, wherein the drawbacks may include complicated processes, or difficulties developing an RNA-structure-specific antibody resulting from an instable RNA structure. Thus, the method of the present invention may be utilized in the study of gene expression in a variety of diseases, in the detection of diagnostic markers of diseases, and in the evaluation of drug efficacy.
    • 本发明涉及一种新型RNA结合蛋白,涉及包含其的用于检测微小RNA的组合物以及使用其检测微小RNA的无标记检测方法。 根据本发明,使用作为包含PAZ结构域和双链RNA结合结构域并与具有突出端3'末端的双链RNA结合的融合蛋白的RNA结合蛋白检测微小RNA的方法是 用于检测没有酶标记过程或酶促扩增反应的微RNA的无标记检测方法,其可以克服常规微RNA分析方法的缺点,即在酶标记之后分析微小RNA的方法或将抗体偶联到微小RNA上的方法,其中 缺点可能包括复杂的过程,或由不稳定的RNA结构产生的RNA结构特异性抗体的困难。 因此,本发明的方法可用于研究各种疾病中的基因表达,检测疾病的诊断标志物和药物功效的评价。