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公开(公告)号:US20190100724A1
公开(公告)日:2019-04-04
申请号:US16082837
申请日:2017-02-17
Applicant: KEIO UNIVERSITY , OSAKA UNIVERSITY
Inventor: Toshiro SATO , Mami MATANO , Shinya SUGIMOTO , Junichi TAKAGI
Abstract: The present invention provides a cell culture medium with which serum-free long-term culture of an epithelial stem cell, an epithelial cancer cell, or a tissue containing at least one thereof can be achieved. The cell culture medium of the present invention includes: a Wnt agonist composed of a complex of Wnt protein and afamin, which is a substance capable of stabilizing the Wnt protein, and R-spondin; and at least one selected from the group consisting of a mitogenic growth factor, a bone morphogenetic protein (BMP) inhibitor, a transforming growth factor-β (TGF-β) inhibitor, and a p38 inhibitor.
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公开(公告)号:US20240360222A1
公开(公告)日:2024-10-31
申请号:US18662493
申请日:2024-05-13
Applicant: OSAKA UNIVERSITY
Inventor: Naoki HOSEN , Haruo SUGIYAMA , Atsushi KUMANOGOH , Junichi TAKAGI
CPC classification number: C07K16/2839 , A61K35/17 , A61K39/0011 , A61P35/00 , C07K19/00 , C12N5/10 , C12N15/09 , A61K2039/505 , A61K2039/5156 , A61K2039/5158 , C07K16/30 , C07K2317/34 , C07K2317/565 , C07K2317/622 , C07K2317/73 , C07K2317/92 , C07K2319/03 , C07K2319/33
Abstract: Provided is an active ingredient of a pharmaceutical composition for treating myeloma. Specifically, provided is an antibody whose epitope is present in the region of the amino acid residue positions 20 to 109 of human integrin β7.
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公开(公告)号:US20190390160A1
公开(公告)日:2019-12-26
申请号:US16565898
申请日:2019-09-10
Applicant: OSAKA UNIVERSITY
Inventor: Junichi TAKAGI , Emiko MIHARA , Akira KIKUCHI
Abstract: Provided is a novel method for producing a Wnt protein, which method comprises (1) a step of performing affinity purification targeting afamin to obtain a Wnt protein from a culture product, and/or (2) a step of performing affinity purification to obtain a Wnt protein in the form of a complex with afamin from a culture product. The method enables a Wnt protein having high Wnt activity to be produced in a simple and brief manner without use of special equipment.
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公开(公告)号:US20250136674A1
公开(公告)日:2025-05-01
申请号:US18835365
申请日:2022-02-03
Applicant: Kyoto University , University of Fukui , Aichi Prefecture , Osaka University
Inventor: Katsu TAKAHASHI , Manabu SUGAI , Yoshihito TOKITA , Junichi TAKAGI , Emiko MIHARA
Abstract: Provided are: an antibody which specifically binds to and neutralizes USAG-1 or an antigen-binding fragment thereof; and a pharmaceutical composition containing the antibody or the antigen-binding fragment.
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公开(公告)号:US20220204346A1
公开(公告)日:2022-06-30
申请号:US17441971
申请日:2020-03-27
Applicant: OSAKA UNIVERSITY
Inventor: Tsuyoshi INOUE , Haruyasu ASAHARA , Kei OHKUBO , Kenji IWASAKI , Naoyuki MIYAZAKI , Mika HIROSE , Atsushi NAKAGAWA , Junichi TAKAGI , Takefumi DOI , Hiroaki ADACHI
IPC: C01B32/156 , C01B32/05 , C01B32/168 , C01B32/194 , H01J37/20
Abstract: The present invention provides a method for producing a substance with a modified carbon allotrope surface that can suppress or prevent uneven distribution, uneven orientation, and the like of a structural analysis target substance in a structural analysis by cryo-electron microscopy. A method for producing a substance with a modified carbon allotrope surface of the present invention includes: the step of surface-treating by reacting a carbon allotrope surface with a halogen oxide radical, wherein the carbon allotrope surface is modified by the surface-treating.
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公开(公告)号:US20200283533A1
公开(公告)日:2020-09-10
申请号:US16808451
申请日:2020-03-04
Applicant: OSAKA UNIVERSITY
Inventor: Naoki HOSEN , Haruo SUGIYAMA , Atsushi KUMANOGOH , Junichi TAKAGI
Abstract: Provided is an active ingredient of a pharmaceutical composition for treating myeloma. Specifically, provided is an antibody whose epitope is present in the region of the amino acid residue positions 20 to 109 of human integrin β7.
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公开(公告)号:US20190276561A1
公开(公告)日:2019-09-12
申请号:US16345639
申请日:2017-11-07
Applicant: FUJIFILM WAKO PURE CHEMICAL CORPORATION , OSAKA UNIVERSITY
Inventor: Junichi TAKAGI
Abstract: An object of the present invention is to provide a fragment antibody which can be conveniently produced as one having antigen-binding activity, and which has a greater ability to crystallize itself alone or as a complex with an antigen molecule than that of Fv-clasp (v1) even in a case where the fragment antibody is obtained in an E. coli expression system. The present invention relates to a fragment antibody including a complex of a peptide (VH(112C)-SARAH) in which an N-terminus of a SARAH domain is linked to a C-terminus of a heavy chain domain (VH region) of an antibody, and an amino acid residue of antibody residue 112 according to Chothia numbering scheme in the VH region is mutated to cysteine; and a peptide (VL-SARAH(37C)) in which an N-terminus of a SARAH domain is linked to a C-terminus of a light chain domain (VL region) of an antibody, and an amino acid residue at position 13 from the C-terminus in the SARAH domain is mutated to cysteine.
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公开(公告)号:US20180230216A1
公开(公告)日:2018-08-16
申请号:US15751574
申请日:2016-08-02
Applicant: OSAKA UNIVERSITY
Inventor: Naoki HOSEN , Haruo SUGIYAMA , Atsushi KUMANOGOH , Junichi TAKAGI
CPC classification number: C07K16/2839 , A61K35/17 , A61K39/0011 , A61K2039/505 , A61K2039/5156 , A61K2039/5158 , A61P35/00 , C07K16/30 , C07K19/00 , C07K2317/34 , C07K2317/565 , C07K2317/622 , C07K2317/73 , C07K2317/92 , C07K2319/03 , C07K2319/33 , C12N5/10 , C12N15/09
Abstract: Provided is an active ingredient of a pharmaceutical composition for treating myeloma. Specifically, provided is an antibody whose epitope is present in the region of the amino acid residue positions 20 to 109 of human integrin β7.
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公开(公告)号:US20170355953A1
公开(公告)日:2017-12-14
申请号:US15539241
申请日:2015-12-24
Applicant: OSAKA UNIVERSITY
Inventor: Junichi TAKAGI , Emiko MIHARA , Akira KIKUCHI
Abstract: Provided is a novel method for producing a Wnt protein, which method comprises (1) a step of performing affinity purification targeting afamin to obtain a Wnt protein from a culture product, and/or (2) a step of performing affinity purification to obtain a Wnt protein in the form of a complex with afamin from a culture product. The method enables a Wnt protein having high Wnt activity to be produced in a simple and brief manner without use of special equipment.
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