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Gibco™ CTS™ KnockOut™ SR XenoFree Medium Non-distribution product as customer accommodation. Green Product

CTS™ KnockOut™ SR XenoFree Medium

Manufacturer:  Gibco™ 12618013

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Catalog No. 12-618-013


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Description

Description

GIBCO™ CTS™ KnockOut™ SR XenoFree Medium, when formulated as a complete medium, enables the growth and expansion of human embryonic stem cells (hESC) and human induced pluripotent stem cells (hiPSC) in a cell culture medium containing only human-derived or human recombinant proteins, to facilitate the transition of hESC and hiPSC research from the bench to the clinic.

The CTS™ product line enables you to reduce your burden in qualifying reagents during your transition from research applications to clinical applications.

  • Defined, xenofree medium for hESC⁄iPSC stem cell culture.
  • First-to-market xenofree hESC⁄iPSC product intended for Ex Vivo tissue and cell culture processing applications.

    CTS™ KnockOut™ SR XenoFree Medium does not contain bovine or other non-human, animal-derived components. Besides pluripotent stem cell culture expansion and maintenance, CTS™ KnockOut™ SR XenoFree Medium can be used for hESC⁄hiPSC cryopreservation, derivation, and differentiation studies.

    GIBCO™ CTS™ products are of high quality, and are supplied with harmonized documentation such as Certificates of Analysis, Certificates of Origin, and access to authorization letters for our Drug Master Files, as appropriate.

    For human ex vivo tissue and cell culture processing applications. CAUTION: Not intended for direct administration to humans or animals.
  • Specifications

    Specifications

    Serum-Free, Xeno-Free
    cGMP for medical devices, 21 CFR Part 820 and ISO 13485
    ES Cell-Qualified
    Dry Ice
    Frozen
    Cell Therapy Research
    Sterile
    -5 to -20°C
    CTS™, KnockOut™
    500mL
    Human
    No Glutamine
    Stem Cells (iPS - Induced Pluripotent Stem), Stem Cells (Embryonic)
    Documents
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    For human ex vivo tissue and cell culture processing applications. CAUTION: When used as a medical device, Federal Law restricts this device to sale by or on the order of a physician.