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1.
公开(公告)号:US20060228359A1
公开(公告)日:2006-10-12
申请号:US11381977
申请日:2006-05-05
申请人: Reiner Gentz , Brent Kreider , Jun Zhang , Michael Antonaccio , Donna Mendrik , Pablo Jimenez , Vikram Patel , Craig Rosen , Mark Adams , Haodong Li , Steven Ruben
发明人: Reiner Gentz , Brent Kreider , Jun Zhang , Michael Antonaccio , Donna Mendrik , Pablo Jimenez , Vikram Patel , Craig Rosen , Mark Adams , Haodong Li , Steven Ruben
IPC分类号: A61K39/395 , G01N33/53 , C12N5/06 , C07K16/24
CPC分类号: G01N33/6863 , A61K38/00 , A61K48/00 , C07K1/113 , C07K1/36 , C07K14/50 , C07K14/521 , C07K14/523 , C07K16/24 , C07K2319/00 , C12N15/72 , C12N2799/026 , G01N2333/52
摘要: There are disclosed therapeutic compositions and methods using isolated nucleic acid molecules encoding a human myeloid progenitor inhibitory factor-1 (MPIF-1) polypeptide (previously termed MIP-3 and chemokine β8 (CKβ8 or ckb-8)); a human monocyte-colony inhibitory factor (M-CIF) polypeptide (previously termed MIP1-γ and chemokine β1(CKβ1 or ckb-1)), and a macrophage inhibitory protein-4 (MIP-4), as well as MPIF-1, M-CIF and/or MIP-4 polypeptides themselves, as are vectors, host cells and recombinant methods for producing the same.
摘要翻译: 公开了使用编码人骨髓祖细胞抑制因子-1(MPIF-1)多肽(以前称为MIP-3和趋化因子β8(CKbeta8或ckb-8))的分离的核酸分子的治疗组合物和方法。 人单核细胞集落抑制因子(M-CIF)多肽(以前称为MIP1-γ和趋化因子β1(CKbeta1或ckb-1))和巨噬细胞抑制蛋白-4(MIP-4)以及MPIF-1 ,M-CIF和/或MIP-4多肽本身,以及用于产生它们的载体,宿主细胞和重组方法。
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公开(公告)号:US20060035337A1
公开(公告)日:2006-02-16
申请号:US11247235
申请日:2005-10-12
申请人: Haodong Li , Brent Kreider
发明人: Haodong Li , Brent Kreider
CPC分类号: C07K14/521 , A61K38/00 , C07K14/522 , C07K14/523 , C07K14/5421 , Y02A50/473 , Y10S930/14
摘要: There are disclosed therapeutic compositions and methods using isolated nucleic acid molecules encoding a human chemokine beta-11 (Ck beta-11) polypeptide and a human leukocyte adhesion inhibitor-1 (LAI-1) polypeptide (previously termed chemokine α1 (CKα1 or cka-1), as well as Ck beta-11 and/or LAI-1 polypeptides themselves, as are vectors, host cells and recombinant methods for producing the same.
摘要翻译: 公开了使用编码人趋化因子β-11(Ckβ-11)多肽和人白细胞粘附抑制剂-1(LAI-1)多肽的分离的核酸分子的治疗组合物和方法(先前称为趋化因子α1(CKalpha1或cka- 1)以及Ckβ-11和/或LAI-1多肽本身,以及用于产生它们的载体,宿主细胞和重组方法。
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公开(公告)号:US20070048256A1
公开(公告)日:2007-03-01
申请号:US11537681
申请日:2006-10-02
申请人: Ying-Fei Wei , Brent Kreider , Craig Rosen
发明人: Ying-Fei Wei , Brent Kreider , Craig Rosen
CPC分类号: C07K14/523
摘要: The present invention concerns a member of the human chemokine CC protein family. In particular, isolated nucleic acid molecules are provided encoding the chemokine β-15 protein. Chemokine β-15 polypeptides are also provided. The invention further concerns diagnostic methods for detecting thymus disorders and therapeutic methods for modulating bone marrow cell proliferation and differentiation.
摘要翻译: 本发明涉及人趋化因子CC蛋白家族的成员。 特别地,提供编码趋化因子β-15蛋白的分离的核酸分子。 还提供趋化因子β-15多肽。 本发明还涉及用于检测胸腺疾病的诊断方法和用于调节骨髓细胞增殖和分化的治疗方法。
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公开(公告)号:US20080226586A9
公开(公告)日:2008-09-18
申请号:US11537681
申请日:2006-10-02
申请人: Ying-Fei Wei , Brent Kreider , Craig Rosen
发明人: Ying-Fei Wei , Brent Kreider , Craig Rosen
CPC分类号: C07K14/523
摘要: The present invention concerns a member of the human chemokine CC protein family. In particular, isolated nucleic acid molecules are provided encoding the chemokine β-15 protein. Chemokine β-15 polypeptides are also provided. The invention further concerns diagnostic methods for detecting thymus disorders and therapeutic methods for modulating bone marrow cell proliferation and differentiation.
摘要翻译: 本发明涉及人趋化因子CC蛋白家族的成员。 特别地,提供了编码趋化因子β-15蛋白的分离的核酸分子。 还提供趋化因子β-15多肽。 本发明还涉及用于检测胸腺疾病的诊断方法和用于调节骨髓细胞增殖和分化的治疗方法。
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公开(公告)号:US06846655B1
公开(公告)日:2005-01-25
申请号:US09434834
申请日:1999-11-05
CPC分类号: C12N15/1093 , Y10T436/143333
摘要: Disclosed herein is a method for generating a nucleic acid library, the method involving: (a) providing a population of single-stranded nucleic acid templates, each of the templates including a coding sequence and an operably linked promoter sequence; (b) hybridizing to the population of single-stranded nucleic acid templates a mixture of substantially complementary single-stranded nucleic acid fragments, the fragments being shorter in length than the nucleic acid template; (c) contacting each of the hybridization products of step (b) with both a DNA polymerase which lacks strand displacement activity and a DNA ligase under conditions in which the fragments act as primers for the completion of a second nucleic acid strand which is substantially complementary to the nucleic acid template; and (d) contacting the products of step (c) with RNA polymerase to generate an RNA library, the library being transcribed from the second nucleic acid strand.
摘要翻译: 本文公开了一种产生核酸文库的方法,所述方法包括:(a)提供单链核酸模板群,每个模板包括编码序列和可操作地连接的启动子序列; (b)与单链核酸模板群体杂交基本互补的单链核酸片段的混合物,其长度比核酸模板短; (c)步骤(b)的每个杂交产物与缺少链置换活性的DNA聚合酶和DNA连接酶在条件下接触,其中片段充当用于完成基本上互补的第二核酸链的引物 至核酸模板; 和(d)使步骤(c)的产物与RNA聚合酶接触以产生RNA文库,该文库从第二个核酸链转录。
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