METHOD FOR ISOLATING URETERIC BUD TIP CELLS

    公开(公告)号:US20220380732A1

    公开(公告)日:2022-12-01

    申请号:US17765358

    申请日:2020-09-30

    Abstract: Provided is a method for isolating a ureteric bud tip cell from cells, a tissue, or an organoid comprising the ureteric bud tip cell, comprising the following steps of contacting the cells, tissue, or organoid comprising the ureteric bud tip cell with a very low density lipoprotein receptor (VLDL-R) binding agent, and isolating the ureteric bud tip cell using the binding agent as an indicator.

    STEPWISE METHOD FOR INDUCING CHOLANGIOCYTE PROGENITORS FROM HEPATOBLASTS

    公开(公告)号:US20200010807A1

    公开(公告)日:2020-01-09

    申请号:US16461905

    申请日:2017-11-21

    Abstract: Provided are: a method for producing biliary epithelial progenitor cells, said method comprising a step for culturing hepatoblasts in a medium containing TGFβ and EGF; and a method for constructing a three-dimensional duct-like structure of biliary epithelial progenitor cells, said method comprising a step for culturing hepatoblasts or biliary epithelial progenitor cells in a medium containing HGF, EGF, a Notch inhibitor and a GSK3 inhibitor in the presence of a three-dimensional scaffold material.

    METHOD FOR PRODUCING RENAL PROGENITOR CELLS
    16.
    发明申请

    公开(公告)号:US20180273905A1

    公开(公告)日:2018-09-27

    申请号:US15758580

    申请日:2016-09-09

    Abstract: An object of the present invention resides in providing a method for acquiring and producing high-purity renal progenitor cells from a renal progenitor cell population into which pluripotent stem cells are induced to differentiate, by identifying a cell surface antigen marker specific to renal progenitor cells.A method for producing renal progenitor cells into which pluripotent stem cells are induced to differentiate, the method comprising the steps of:(i) culturing the pluripotent stem cells under conditions that induce differentiation into renal progenitor cells; and (ii) sorting a cell population from the cells obtained at step (i), by using at least one cell surface marker selected from the group consisting of CD9(−), CD55(−), CD106(+), CD140a(+), CD140b(+), CD165(+), CD271(+) and CD326(−).

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