MASS PRODUCTION METHOD OF PLURIPOTENT STEM CELL STOCK

    公开(公告)号:US20240352427A1

    公开(公告)日:2024-10-24

    申请号:US18747005

    申请日:2024-06-18

    CPC classification number: C12N5/0696 C12N2501/603 C12N2501/727

    Abstract: The purpose of the present invention is to produce a large amount of a high-quality pluripotent stem cell stock. A mass production method of a pluripotent stem cell stock that comprises thawing starting cells followed by adhesion culture to thereby stabilize the cell conditions, and then growing the cells to a cell count that enables suspension culture. Subsequently, the cells are suspension cultured while precisely controlling the culture environment to thereby grow a large number of high-quality cells. Then, a stock is prepared at a low temperature from the cells having been grown by the suspension culture.

    PRODUCTION METHOD FOR INDUCED PLURIPOTENT STEM CELLS

    公开(公告)号:US20250145965A1

    公开(公告)日:2025-05-08

    申请号:US18835550

    申请日:2023-02-02

    Abstract: To provide a method for producing induced pluripotent stem cells (iPS cells) that can initialize somatic cells without using feeder cells or a substrate. For production of iPS cells, the following steps are carried out: I. introducing an initialization gene into a somatic cell; and II. performing initialization and amplification culture of the cell into which the gene has been introduced, in a liquid medium comprising at least one of a protein kinase Cβ (PKCβ) inhibitor and a WNT inhibitor under a suspension culture condition.

    METHOD FOR PRODUCING PLURIPOTENT STEM CELL POPULATION

    公开(公告)号:US20240191185A1

    公开(公告)日:2024-06-13

    申请号:US18283744

    申请日:2022-03-25

    CPC classification number: C12N5/0606 C12N5/0696 C12N2500/02

    Abstract: The pluripotent stem cell culture environment is appropriately controlled to improve production efficiency, and to suppress cell death when passaging pluripotent stem cells from suspension culture. Pluripotent stem cells subjected to suspension culture in a perfusion mode under appropriate medium perfusion conditions are passaged in the subsequent culture step, thereby improving passage efficiency. By strictly controlling the amount of medium perfused in line with the progress of culture of pluripotent stem cells and/or adjusting the amount of carbon dioxide gas supplied in line with the progress of culture of pluripotent stem cells, culture efficiency and productivity can be remarkably improved.

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