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iPS-27 Cells T2008|产品详情|进口橙子视频旧款采购网




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    上海橙子视频app安卓下载生物科技公司
    Tel:400-968-7988    021-33779008
    iPS-27 Cells
    品牌:Abmgood
    货号:T2008
    规格:
    货期:

    iPS-27 Cells

    商品详情 参考文献 相关资料
    Print Version
    Safety Biosesafety Level II
    Organism Human
    Source Organ Fetal Lung Fibroblasts (MRC-5)
    Picture
    Image
    Concentration 106 Cells/ml
    Induction iPS-27 was generated using lentiviral transduction of human fetal lung fibroblasts with cMYC, KLF4, OCT4 and SOX2.
    Pluripotency Positive for markers Nanog, Tra-1-60, Tra-1-80 and SSEA-3 by immunofluorescence and flow cytometry. Capable of differentiating into derivatives of the 3 germ layers.
    Propagation The base medium for this cell line is Prigrow IV medium available from ABM (TM004). To make the complete growth medium, add the following components to the base medium: serum replacer to a final concentration of 20%; b-FGF to a final concentration of 6ng/ml; 1 mM L-glutamine and 2-mercaptoethanol solution; 1X Non-essential amino acids. Sterilize the media through a 0.22 micron filter before use. This cell line needs to be cultured on mouse embryonic fibroblasts (ABM T2001) feeder cells. Atmosphere:air: 95%, CO2: 5%; Temperature: 37.0°C.
    Subculturing 1. Remove and discard culture medium.

    2. Add 2.0mL of Dispase solution to flask and incubate the cells at 37°C to facilitate dispersal. Observe cells under an inverted microscope until cell layer is dispersed.

    3.Transfer the dispase solutions containing colonies into a conical tube.

    4. Centrifuge cells at 1000rpm for 3 minutes to pellet.

    5. Gently aspirate out the solution, leaving pellet undisturbed.

    6. Resuspend pellet in fresh culture medium and plate on MEF feeder plates.

    7. Incubate cultures at 37°C.
    Storage -180°C
    Shipping On Dry Ice
    Notes For Research Use Only, not for therapeutic or diagnostic purposes.
    References 1. Stuart M Chambers, Christopher A Fasano, Eirni P Papapetrou, Mark Tomishima, Michel Sadelain and Lorenz Studer. Highly efficient neural conversion of human ES and iPS cells by dual inhibition of SMAD signaling. Nat Biotechnol. 26, 275-280 (2009).

    2. Papapetrou EP, Tomishima MJ, Chambers SM, Mica Y, Reed E, Menon J, Tabar V, Mo Q, Studer L, Sadelain M. Stoichiometric and temporal requirements of Oct4, Sox2, Klf4, and c-Myc expression for efficient human iPSC induction and differentiation. Proc Natl Acad Sci U S A. Aug 4;106(31):12759-64. (2009).
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