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    • 1. 发明授权
    • Methods and compositions for interaction trap assays
    • 相互作用阱测定法的方法和组成
    • US07393318B2
    • 2008-07-01
    • US10801994
    • 2004-03-16
    • J. Keith JoungJeffrey MillerCarl O. Pabo
    • J. Keith JoungJeffrey MillerCarl O. Pabo
    • C40B40/08C40B40/06C40B40/10C07H21/04
    • G01N33/502C12N15/1055C12Q1/6897G01N33/50G01N33/5008C12Q2565/201
    • The present invention provides methods and compositions for interaction trap assays for detecting protein-protein, protein-DNA, or protein-RNA interactions. The methods and compositions of the invention may also be used to identify agents which may agonize or antagonize a protein-protein, protein-DNA, or protein-RNA interaction. In certain embodiments, the interaction trap system of the invention is useful for screening libraries with greater than 107 members. In other embodiments, the interaction trap system of the invention is used in conjunction with flow cytometry. The invention further provides a means for simultaneously screening a target protein or nucleic acid sequence for the ability to interact with two or more test proteins or nucleic acids.
    • 本发明提供了用于检测蛋白质 - 蛋白质,蛋白质-DNA或蛋白质 - RNA相互作用的相互作用阱测定法的方法和组合物。 本发明的方法和组合物还可用于鉴定可能激动或拮抗蛋白质 - 蛋白质,蛋白质-DNA或蛋白质 - RNA相互作用的试剂。 在某些实施方案中,本发明的相互作用捕获系统可用于筛选具有大于10个成员的文库。 在其它实施方案中,本发明的相互作用阱系统结合流式细胞术使用。 本发明还提供了用于同时筛选靶蛋白或核酸序列以获得与两种或多种测试蛋白或核酸相互作用的能力的方法。
    • 2. 发明授权
    • Methods and compositions for interaction trap assays
    • 相互作用阱测定法的方法和组成
    • US07297491B2
    • 2007-11-20
    • US10915233
    • 2004-08-10
    • J. Keith JoungJeffrey MillerCarl O. Pabo
    • J. Keith JoungJeffrey MillerCarl O. Pabo
    • C12Q1/68
    • C12N15/1055C12Q1/6897G01N33/50G01N33/5008G01N33/502C12Q2565/201
    • The present invention provides methods and compositions for interaction trap assays for detecting protein-protein, protein-DNA, or protein-RNA interactions. The methods and compositions of the invention may also be used to identify agents which may agonize or antagonize a protein-protein, protein-DNA, or protein-RNA interactions. In certain embodiments, the interaction trap system of the invention is useful for screening libraries with greater than 107 members. In other embodiments, the interaction trap system of the invention is used in conjunction with flow cytometry. The invention further provides a means for simultaneously screening a target protein or nucleic acid sequence for the ability to interact with two or more test proteins or nucleic acids.
    • 本发明提供了用于检测蛋白质 - 蛋白质,蛋白质-DNA或蛋白质 - RNA相互作用的相互作用阱测定法的方法和组合物。 本发明的方法和组合物还可用于鉴定可能激动或拮抗蛋白质 - 蛋白质,蛋白质-DNA或蛋白质 - RNA相互作用的试剂。 在某些实施方案中,本发明的相互作用捕获系统可用于筛选具有大于10个成员的文库。 在其它实施方案中,本发明的相互作用阱系统结合流式细胞术使用。 本发明还提供了用于同时筛选靶蛋白或核酸序列以获得与两种或多种测试蛋白或核酸相互作用的能力的方法。
    • 3. 发明申请
    • ENGINEERING OF ZINC FINGER ARRAYS BY CONTEXT-DEPENDENT ASSEMBLY
    • 按照附件大会编制ZINC指纹阵列
    • US20120178647A1
    • 2012-07-12
    • US13386995
    • 2010-08-03
    • J. Keith JoungJeffry D. Sander
    • J. Keith JoungJeffry D. Sander
    • C40B30/04C12N15/62C07K19/00C12N9/10C12N5/071C12N9/16C12N9/14C12P19/34C40B40/10C12P21/00C12N9/12
    • C12N15/1093C40B40/08C40B50/06
    • A method of designing a multi-zinc-finger polypeptide predicted to bind to a sequence of interest that has at least three subsites includes the steps of: a) providing a nucleotide sequence of interest having first, second, and third consecutive subsites, wherein each of the first and third subsites are adjacent to the second subsite; b) identifying first and second adjacent zinc finger polypeptide sequences previously shown to bind to the first and second subsites in the context of a multi-zinc finger polypeptide; c) identifying a third zinc finger polypeptide previously shown to bind to a third subsite adjacent to the second subsite when present in the context of a multi-zinc finger polypeptide adjacent to the second zinc finger polypeptide; and d) combining the first, second, and third zinc finger polypeptide sequences in linear order, thereby designing a multi-zinc finger polypeptide predicted to bind to the sequence of interest.
    • 设计预期结合具有至少三个亚位的感兴趣序列的多锌指多肽的方法包括以下步骤:a)提供具有第一,第二和第三连续子区的感兴趣的核苷酸序列,其中每个 的第一和第三子集与第二子网相邻; b)鉴定在多锌指多肽的上下文中先前显示结合第一和​​第二子集的第一和第二相邻锌指多肽序列; c)鉴定当与多于第二锌指多肽相邻的多锌指多肽的情况下,先前显示的第三锌指多肽与第二亚位点相邻的第三子部位结合; 和d)以线性顺序组合第一,第二和第三锌指多肽序列,从而设计预测结合感兴趣序列的多锌指多肽。
    • 5. 发明申请
    • Methods of Transcription Activator Like Effector Assembly
    • 转录激活剂与效应器装配方法
    • US20140274812A1
    • 2014-09-18
    • US14232067
    • 2012-07-12
    • J. Keith JoungJeffry D. Sander
    • J. Keith JoungJeffry D. Sander
    • C07K14/195C12N15/10
    • C07K14/195C07K2319/00C07K2319/24C07K2319/41C07K2319/43C07K2319/80C12N9/22C12N15/1093C12N15/66C12P19/34C12P21/02C12Q1/6806C12Y301/00C40B40/08C40B50/06C12Q2521/501C12Q2563/149
    • The disclosure describes methods that include providing a first nucleic acid having a sequence encoding a first set comprising one or more transcription activator-like effector (TALE) repeat domains and/or one or more portions of one or more TALE repeat domains; contacting the first nucleic acid with a first enzyme, wherein the first enzyme creates a first ligatable end; providing a second nucleic acid having a sequence encoding a second set comprising one or more TALE repeat domains and/or one or more portions of one or more TALE repeat domains; contacting the second nucleic acid with a second enzyme, wherein the second enzyme creates a second ligatable end, and wherein the first and second ligatable ends are compatible; and ligating the first and second nucleic acids through the first and second ligatable ends to produce a first ligated nucleic acid, wherein the first ligated nucleic acid is linked to a solid support, and wherein the first ligated nucleic acid encodes a polypeptide comprising said first and second sets.
    • 本公开描述了包括提供具有编码包含一个或多个转录激活子样效应子(TALE)重复结构域和/或一个或多个TALE重复结构域的一个或多个部分的第一组的序列的第一核酸的方法; 使所述第一核酸与第一酶接触,其中所述第一酶产生第一可结合末端; 提供具有编码包含一个或多个TALE重复结构域和/或一个或多个TALE重复结构域的一个或多个部分的第二组的序列的第二核酸; 使所述第二核酸与第二酶接触,其中所述第二酶产生第二可连接末端,并且其中所述第一和第二可连接末端是相容的; 以及通过所述第一和第二可连接末端连接所述第一和第二核酸以产生第一连接的核酸,其中所述第一连接的核酸与固体支持物连接,并且其中所述第一连接的核酸编码包含所述第一和第二核酸的多肽 第二套
    • 7. 发明授权
    • Methods and compositions for interaction trap assays
    • 相互作用阱测定法的方法和组成
    • US07029847B2
    • 2006-04-18
    • US09990762
    • 2001-11-14
    • J. Keith JoungJeffrey MillerCarl O. Pabo
    • J. Keith JoungJeffrey MillerCarl O. Pabo
    • C12Q1/68G01N33/53G01N33/567
    • C12N15/1055C12Q1/6897G01N33/50G01N33/5008G01N33/502C12Q2565/201
    • The present invention provides methods and compositions for interaction trap assays for detecting protein-protein, protein-DNA, or protein-RNA interactions. The methods and compositions of the invention may also be used to identify agents which may agonize or antagonize a protein-protein, protein-DNA, or protein-RNA interaction. In certain embodiments, the interaction trap system of the invention is useful for screening libraries with greater than 107 members. In other embodiments, the interaction trap system of the invention is used in conjunction with flow cytometry. The invention further provides a means for simultaneously screening a target protein or nucleic acid sequence for the ability to interact with two or more test proteins or nucleic acids.
    • 本发明提供了用于检测蛋白质 - 蛋白质,蛋白质-DNA或蛋白质 - RNA相互作用的相互作用阱测定法的方法和组合物。 本发明的方法和组合物还可用于鉴定可能激动或拮抗蛋白质 - 蛋白质,蛋白质-DNA或蛋白质 - RNA相互作用的试剂。 在某些实施方案中,本发明的相互作用捕获系统可用于筛选具有大于10个成员的文库。 在其它实施方案中,本发明的相互作用阱系统结合流式细胞术使用。 本发明还提供了用于同时筛选靶蛋白或核酸序列以获得与两种或多种测试蛋白或核酸相互作用的能力的方法。