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COACTIVATOR OF NUCLEAR RECEPTORS

机译:核受体的活化剂

摘要

A nucleic acid (I): (a) encoding a polypeptide of Seq. ID No. 2 (2055 amino acids, given in the specification); (b) of Seq. ID No. 1 (6995 base pairs, given in the specification); (c) that hybridizes with one of (a) and/or (b) under stringent conditions; or (d) comprising one of (a)-(c) with degeneration of the genetic code appropriate nucleotide sequence, is new. Independent claims are also included for: (1) a polypeptide encoded by the nucleic acid (I); (2) a vector represented in Seq. ID No. 2, that contains at least one copy of (I); (3) a cell transfected with a nucleic acid (I) or with the vector (2); (4) use of a cell (3) to express (I); (5) use of (1) or a part of it for the production of antibodies; (6) an antibody against (1); (7) use of (6) for the detection of (1); (8) use of a probe with nucleic acid sequences which are complementary to the nucleic acid sequence, which encode (1), for the production of a reagent for proving the presence of mRNA; (9) use of a (I) or (1) for the treatment of steroidal hormone dependent illnesses; (10) use of (I), (1), or (6) for the identification of the effectiveness of a (1); (11) a test system for the detection of the effect of (1) in a cell where a reporter gene is expressed in a cell, which if it contains no or only a little of a nuclear receptor, is transfected additionally with a vector, which contains the DNA of the nuclear receptor, the cell in the presence or absence of test substances is cultivated and the change of the expression of the reporter gene is measured; and (12) process for the supply of a pharmaceutical means, comprising that substances are brought into contact with a test system of (11), the effect of the substances on the test system compared with controls measured, a substance which shows a modulation of the activity of the polypeptide identified and mixed with usual formulation materials.
机译:核酸(I):(a)编码Seq。的多肽。 ID 2号(规范中给出的2055个氨基酸); (b)Seq。 ID号1(6995个碱基对,在规范中给出); (c)在严格条件下与(a)和/或(b)之一杂交;或(d)包含(a)-(c)之一,且其遗传密码具有适当的核苷酸序列的简并,是新的。还包括以下方面的独立权利要求:(1)由核酸(I)编码的多肽; (2)式中表示的向量。 ID号2,至少包含一份(I); (3)用核酸(I)或载体(2)转染的细胞。 (4)使用细胞(3)表达(I); (5)将(1)或其中一部分用于产生抗体; (6)针对(1)的抗体; (7)将(6)用于检测(1); (8)具有与编码(1)的核酸序列互补的核酸序列的探针在产生证明mRNA存在的试剂中的用途; (9)将(I)或(1)用于治疗类固醇激素依赖性疾病的用途; (10)使用(I),(1)或(6)来识别(1)的有效性; (11)一种用于检测细胞中(1)的作用的测试系统,其中在细胞中表达报告基因,如果该报告基因不包含或仅包含少量核受体,则用载体另外转染,含有核受体的DNA,培养存在或不存在受试物质的细胞,并测定报告基因表达的变化。 (12)提供药物的方法,包括使所述物质与(11)的测试系统接触,与所测量的对照相比,所述物质对测试系统的影响是显示出对药物的调节的物质。鉴定多肽的活性,并与常规制剂材料混合。

著录项

  • 公开/公告号NO20023483L

    专利类型

  • 公开/公告日2003-01-24

    原文格式PDF

  • 申请/专利权人 JENAPHARM GMBH & CO KG;

    申请/专利号NO20020003483

  • 发明设计人 OBENDORF MAIK;WOLF SIEGMUND;

    申请日2002-07-22

  • 分类号C12N15/12;C12N15/63;C07K14/47;C07K16/18;A61K38/17;G01N33/50;G01N33/74;

  • 国家 NO

  • 入库时间 2022-08-22 00:02:06

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