NEUTROKINE-ALPHA AND NEUTROKINE-ALPHA SPLICE VARIANT
    6.
    发明申请
    NEUTROKINE-ALPHA AND NEUTROKINE-ALPHA SPLICE VARIANT 有权
    NEUTROKINE-ALPHA和NEUTROKINE-ALPHA SPLICE变体

    公开(公告)号:US20100261207A9

    公开(公告)日:2010-10-14

    申请号:US12295572

    申请日:2007-03-30

    IPC分类号: G01N33/53 G01N33/566

    摘要: The present invention relates to nucleic acid molecules encoding Neutrokine-alpha and/or Neutrokine-alphaSV polypeptides, including soluble forms of the extracellular domain Neutrokine-alpha and/or Neutrokine-alphaSV polypeptides are also provided as are vectors, host cells and recombinant methods for producing the same. The invention further relates to antibodies or portions thereof that specifically bind Neutrokine-alpha and/or Neutrokine-alphaSV and diagnostic and therapeutic methods using these antibodies. Also provided are diagnostic methods for detecting immune system-related disorders and therapeutic methods for treating immune system-related disorders using the compositions of the invention.

    摘要翻译: 本发明涉及编码Neutrokine-α和/或Neutrokine-αSV多肽的核酸分子,包括细胞外结构域Neutrokine-α和/或Neutrokine-αSV多肽的可溶形式,载体,宿主细胞和重组方法 生产相同。 本发明进一步涉及使用这些抗体特异性结合中枢神经素α和/或中枢神经素-αSV的诊断和治疗方法的抗体或其部分。 还提供了用于检测免疫系统相关疾病的诊断方法和使用本发明的组合物治疗免疫系统相关疾病的治疗方法。

    Death domain containing receptor 5
    7.
    发明授权
    Death domain containing receptor 5 失效
    含有受体5的死亡域

    公开(公告)号:US07803615B1

    公开(公告)日:2010-09-28

    申请号:US09042583

    申请日:1998-03-17

    摘要: The present invention relates to novel Death Domain Containing Receptor-5 (DR5) proteins which are members of the tumor necrosis factor (TNF) receptor family, and have now been shown to bind TRAIL. In particular, isolated nucleic acid molecules are provided encoding the human DR5 proteins. DR5 polypeptides are also provided as are vectors, host cells and recombinant methods for producing the same. The invention further relates to screening methods for identifying antagonists and antagonists of DR5 activity.

    摘要翻译: 本发明涉及作为肿瘤坏死因子(TNF)受体家族的成员的新的含有死亡域的受体-5(DR5)蛋白,现在已经显示结合TRAIL。 特别地,提供编码人DR5蛋白的分离的核酸分子。 还提供了DR5多肽,载体,宿主细胞以及用于制备它们的重组方法。 本发明还涉及用于鉴定DR5活性的拮抗剂和拮抗剂的筛选方法。

    NEUTROKINE-ALPHA AND NEUTROKINE-ALPHA SPLICE VARIANT
    8.
    发明申请
    NEUTROKINE-ALPHA AND NEUTROKINE-ALPHA SPLICE VARIANT 有权
    NEUTROKINE-ALPHA和NEUTROKINE-ALPHA SPLICE变体

    公开(公告)号:US20090221008A1

    公开(公告)日:2009-09-03

    申请号:US12295572

    申请日:2007-03-30

    IPC分类号: G01N33/53 G01N33/566

    摘要: The present invention relates to nucleic acid molecules encoding Neutrokine-alpha and/or Neutrokine-alphaSV polypeptides, including soluble forms of the extracellular domain Neutrokine-alpha and/or Neutrokine-alphaSV polypeptides are also provided as are vectors, host cells and recombinant methods for producing the same. The invention further relates to antibodies or portions thereof that specifically bind Neutrokine-alpha and/or Neutrokine-alphaSV and diagnostic and therapeutic methods using these antibodies. Also provided are diagnostic methods for detecting immune system-related disorders and therapeutic methods for treating immune system-related disorders using the compositions of the invention.

    摘要翻译: 本发明涉及编码Neutrokine-α和/或Neutrokine-αSV多肽的核酸分子,包括细胞外结构域Neutrokine-α和/或Neutrokine-αSV多肽的可溶形式,载体,宿主细胞和重组方法 生产相同。 本发明进一步涉及使用这些抗体特异性结合中枢神经素α和/或中枢神经素-αSV的诊断和治疗方法的抗体或其部分。 还提供了用于检测免疫系统相关疾病的诊断方法和使用本发明的组合物治疗免疫系统相关疾病的治疗方法。

    Human Tumor Necrosis Factor Receptor-Like 2

    公开(公告)号:US20090092608A1

    公开(公告)日:2009-04-09

    申请号:US12241203

    申请日:2008-09-30

    摘要: The present invention relates to novel members of the Tumor Necrosis Factor family of receptors. The invention provides isolated nucleic acid molecules encoding a human TR2 receptor and two splice variants thereof. TR2 polypeptides are also provided as are vectors, host cells and recombinant methods for producing the same. The invention further relates to screening methods for identifying agonists and antagonists of TR2 receptor activity. Also provided are diagnostic methods for detecting disease states related to the aberrant expression of TR2 receptors. Further provided are therapeutic methods for treating disease states related to aberrant proliferation and differentiation of cells which express the TR2 receptors.