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    • 3. 发明申请
    • VEGF-LIKE FACTOR ANTIBODIES AND METHODS OF USE THEREOF
    • VEGF-样因子抗体及其使用方法
    • US20110293602A1
    • 2011-12-01
    • US12729708
    • 2010-03-23
    • Yuichi HirataJunichi Nezu
    • Yuichi HirataJunichi Nezu
    • A61K39/395A61P7/00C07K16/18
    • C07K14/52A61K38/00A61K48/00
    • A novel human gene having a significant homology with a VEGF-C gene, a member of the VEGF family, has been isolated by the PCR method using primers designed based on the sequence of EST that is assumed to be homologous with the C-terminal region of the VEGF-C gene. Mouse and rat genes have been isolated based on the human gene isolated as above. A protein encoded by the above human gene has been isolated by introducing the gene into Escherichia coli and expressing it. The isolated protein and genes can be applied to, for example, gene therapy for the VEGF-D deficiency, wound healing, and promotion of collateral vessel formation. Furthermore, VEGF-D protein inhibitors can be used as a novel anticancer drug, etc.
    • 已经通过PCR方法分离了与VEGF-C基因具有显着同源性的新型人基因,该方法使用基于EST序列设计的引物,其被假设与C-末端区域同源 的VEGF-C基因。 已经基于如上分离的人基因分离了小鼠和大鼠基因。 通过将该基因导入大肠杆菌并表达上述人基因编码的蛋白质已被分离。 分离的蛋白质和基因可以应用于例如VEGF-D缺陷的基因治疗,伤口愈合和促进旁路血管形成。 此外,VEGF-D蛋白抑制剂可用作新型抗癌药物等。
    • 5. 发明授权
    • Antibodies that bind to a member of the IL-6/G-CSF/MGF family
    • 结合IL-6 / G-CSF / MGF家族成员的抗体
    • US07750126B2
    • 2010-07-06
    • US11716808
    • 2007-03-12
    • Yuichi Hirata
    • Yuichi Hirata
    • C07K16/24
    • C07K14/54A01K2217/05A61K38/00C07K14/52
    • A full-length cDNA corresponding to an EST (AA418955), which does not show any homology to other proteins in the database but has a weak homology to G-CSF, has been successfully isolated by synthesizing primers based on the EST sequence, and effecting PCR-cloning from a human fetal spleen library. Sequencing of the thus-isolated cDNA and analysis of its structure revealed that the cDNA has typical characteristics of a factor belonging to the IL-6/G-CSF/MGF family. It is also found out that the culture supernatant of said sequence-transfected CHO cells shows a proliferation supporting activity towards bone marrow cells in the coexistence of kit ligand.
    • 已经通过基于EST序列的合成引物成功地分离了对应于EST(AA418955)的全长cDNA,其不与数据库中的其它蛋白质显示任何同源性,但与G-CSF具有弱同源性,并且通过 来自人胎儿脾脏文库的PCR克隆。 这样分离的cDNA的测序及其结构的分析显示cDNA具有属于IL-6 / G-CSF / MGF家族的因子的典型特征。 还发现所述序列转染的CHO细胞的培养上清液在试剂盒配体的共存下显示对骨髓细胞的增殖支持活性。
    • 7. 发明申请
    • Filtration member for inflator and method of manufacturing the same
    • 充气机的过滤构件及其制造方法
    • US20070193235A1
    • 2007-08-23
    • US10596524
    • 2005-01-27
    • Yuichi Hirata
    • Yuichi Hirata
    • B01D50/00B60R21/26B23P15/16
    • B01D39/12B60R21/2644Y10S55/05Y10T29/49604
    • An inflator filter (15) includes a cylindrical body (15a) that is formed by winding a wire (16). The cylindrical body (15a) includes an inner circumferential portion (21) and an outer circumferential portion (22) covering an outer circumferential surface of the inner circumferential portion (21). The inner circumferential portion (21) is formed by superimposing a plurality of first pattern layers (18a) in a radial direction. The outer circumferential portion (22) is formed by superimposing one or more second pattern layers (18b) on an outer circumferential surface of the inner circumferential portion (21) in the radial direction. Each of the first and second pattern layers (18a and 18b) is formed from the wire (16) so as to have meshes. The meshes of each second pattern layer (18b) are smaller than the meshes of the first pattern layers (18a).
    • 充气机过滤器(15)包括通过缠绕线(16)而形成的圆筒体(15a)。 圆筒体(15a)包括内周部(21)和覆盖内周部(21)的外周面的外周部(22)。 内圆周部分(21)通过在径向上叠加多个第一图案层(18a)而形成。 外周部(22)通过在径向上在内周部(21)的外周面上重叠一个以上的第二图案层(18b)而形成。 第一和第二图案层(18a和18b)中的每一个由线(16)形成以具有网格。 每个第二图案层(18b)的网格小于第一图案层(18a)的网格。
    • 8. 发明授权
    • Nucleic acids encoding cytokine-like proteins that promote cell proliferation
    • 编码促进细胞增殖的细胞因子样蛋白的核酸
    • US07252967B2
    • 2007-08-07
    • US10440066
    • 2003-05-15
    • Yuichi Hirata
    • Yuichi Hirata
    • C12P21/02C07H21/04A61K38/18
    • C07K14/54A01K2217/05A61K38/00C07K14/52
    • A full-length cDNA corresponding to an EST (AA418955), which does not show any homology to other proteins in the database but has a weak homology to G-CSF, has been successfully isolated by synthesizing printers based on the EST sequence, and effecting PCR-cloning from a human fetal spleen library. Sequencing of the thus-isolated cDNA and analysis of its structure revealed that the cDNA has typical characteristics of a factor belonging to the IL-6/G-CSF/MGF family. It is also found out that the culture supernatant of said sequence-transfected CHO cells shows a proliferation supporting activity towards bone marrow cells in the coexistence of kit ligand.
    • 已经通过基于EST序列的合成引物成功地分离了对应于EST(AA418955)的全长cDNA,其不与数据库中的其它蛋白质显示任何同源性,但与G-CSF具有弱同源性。 来自人胎儿脾脏文库的PCR克隆。 这样分离的cDNA的测序及其结构的分析显示cDNA具有属于IL-6 / G-CSF / MGF家族的因子的典型特征。 还发现所述序列转染的CHO细胞的培养上清液在试剂盒配体的共存下显示对骨髓细胞的增殖支持活性。
    • 10. 发明申请
    • Novel VEGF-like factors
    • 新型VEGF样因子
    • US20060172343A1
    • 2006-08-03
    • US11397289
    • 2006-04-04
    • Yuichi HirataJunichi Nezu
    • Yuichi HirataJunichi Nezu
    • C07K14/475C07K16/22G01N33/53C07H21/04C12P21/06
    • C07K14/52A61K38/00A61K48/00
    • A novel human gene having a significant homology with a VEGF-C gene, a member of the VEGF family, has been isolated by the PCR method using primers designed based on the sequence of EST that is assumed to be homologous with the C-termial region of the VEGF-C gene. Mouse and rat genes have been isolated based on the human gene isolated as above. A protein encoded by the above human gene has been isolated by introducing the gene into Escherichia coli and expressing it. The isolated protein and genes can be applied to, for example, gene therapy for the VEGF-D deficiency, wound healing, and promotion of collateral vessel formation. Furthermore,VEGF-D protein inhibitorscanbeused as a novel anticancer drug, etc.
    • 已经通过PCR方法分离了与VEGF-C基因具有显着同源性的新型人基因,所述PCR方法使用基于EST序列设计的引物,其被假设为与C末端区域同源 的VEGF-C基因。 已经基于如上分离的人基因分离了小鼠和大鼠基因。 通过将该基因导入大肠杆菌并表达上述人基因编码的蛋白质已被分离。 分离的蛋白质和基因可以应用于例如VEGF-D缺陷的基因治疗,伤口愈合和促进旁路血管形成。 此外,VEGF-D蛋白抑制剂可被用作新型抗癌药物等。