McCoy's 5A (Modified) Medium

McCoy's 5A (Modified) Medium

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  • ¥430
  • Gibco™
  • 16600082
  • 2025年11月06日
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    • 详细信息
    • 技术资料
    • 供应商

      上海觅拓

    • 规格

      500mL

    规格

    Form: Liquid
    Glutamine: L-Glutamine
    HEPES Buffer: No HEPES
    Phenol Red Indicator: Phenol Red
    Product Line: Gibco®
    Product Size: 500 mL
    Sodium Pyruvate Additive: No Sodium Pyruvate
    Volume (Metric): 500 ml
    Green Features: Sustainable packaging
    Shipping Condition: Room Temperature

    描述

    McCoy's 5A (modified) Medium is a general purpose medium that supports the propagation of many types of primary cells, established cell lines, and explants from biopsy tissues. This medium will support the growth of primary mammalian cells derived from normal bone marrow, skin, spleen, kidney, lung, rat embryos, and other tissues.

    This McCoy's 5A is modified as follows:
    With Without
    • High Glucose • Sodium Pyruvate
    • L-glutamine • HEPES
    • Bacto-peptone  
    • Phenol Red  

    The complete formulation is available.

    Using McCoy's 5A (modified) Medium
    Dr. Thomas McCoy originally formulated McCoy's 5A medium as a modification of Basal Medium 5A. Unlike other media, McCoy's 5A contains the reducing agent glutathione, bacto-peptone, and a high level of glucose. This product also includes Dr. Hsu's addition of Hanks' salts to enable use outside a CO2 incubator. McCoy's 5A (modified) Medium requires serum supplementation, commonly with 10% Fetal Bovine Serum (FBS). McCoy's 5A (modified) Medium uses a sodium bicarbonate buffer system (2.2 g/L), and therefore requires a 5–10% CO2 environment to maintain physiological pH.

    cGMP manufacturing and quality system
    McCoy's 5A (modified) Medium is manufactured at a cGMP-compliant facility located in Grand Island, New York. The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards. For supply chain continuity, we offer an identical McCoy's 5A (modified) Medium product made in our Scotland facility (26600-023). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard.

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