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实验试剂 F-12培养基 21700-075 10*1L I

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  • Invitrogen
  • 21700-075
  • 2025年07月11日
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    F-12培养基 21700-075 10*1L Invitrogen
    F-12培养基 21700-075 10*1L Invitrogen

    描述

    Ham's F-12 Nutrient Mixture (F-12) was designed for serum-free single-cell plating of Chinese Hamster Ovary (CHO) cells. F-12 has since been used for serum-free growth of CHO cultures as well as serum-supplemented growth of other mammalian cells, including chondrocytes and rat prostate epithelial cells. Life Technologies offers a variety of Gibco® F-12 modifications for a range of cell culture applications. Find the right formulation using the media selector tool.

    This Ham's F-12 is modified as follows:

    With Without
    • L-glutamine • Sodium Bicarbonate
    • Phenol Red


    The complete formulation is available.

    Compared to other basal media, F-12 contains a wider variety of components, including zinc, putrescine, hypoxanthine, and thymidine. Serum-free growth of CHO cells in F-12 has led to a variety of improved formulations.

    Product Intended Use
    For in vitro diagnostic use. CAUTION: Not for human or animal therapeutic use. Uses other than the intended use may be a violation of local law.

    cGMP Manufacturing and Quality System
    For supply chain continuity, Life Technologies manufactures Gibco® F-12 at two separate facilities located in Grand Island, NY and Scotland, UK. Both sites are compliant with cGMP manufacturing requirements, are certified to ISO 13485, and are registered with the FDA as medical device manufacturers. In addition, the New York facility has ISO 9001 certification.

    Gibco® F-12 contains no proteins or growth factors. Therefore, F-12 requires supplementation, commonly with 10% Fetal Bovine Serum (FBS). F-12 uses a sodium bicarbonate buffer system (1.176 g / L) and therefore requires a 5-10% CO2 environment to maintain physiological pH. Powder forms of Gibco® cell culture medium require sodium bicarbonate supplementation, pH adjustment, and filtration at the time of preparation (see protocol for details).

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    图标文献和实验
    相关实验
    • 用于基因芯片分析的细胞RNA的抽提

      一、实验试剂: Trizol试剂(Invitrogen公司),PBS缓冲液; 二、具体过程: 1、细胞培养结束后,若是贴壁细胞,可以用移液器吸去培养基,并加入3ml左右的PBS洗一次(需要注意的是从冰箱中取出的PBS缓冲液温度要尽量回复到室温,避免给细胞冷的刺激)。吸去PBS后,即可加入适量的Trizol试剂,Trizol的量一般是每10cm 2 的面积加1ml的Trizol;若是悬浮

    • 蛋白印迹(Western Blot)常用试剂

      DMEM高糖 ( 含丙酮酸钠 ) 10×1L 420 Gibco 31600-034 DMEM低糖 10×1L 420 Gibco 21700-075 F12培养基 (Ham) 10×1L 460 Gibco

    • 转染和转染效率测定步骤

      6小时稳定。表6. 在24孔板中转染Invitrogen细胞系的推荐使用量 Table 6Cell Line Cill/well(×10) LIPOFECTAMINE 2000 Reagent(µl)CHO-S 1.5 2.5-3.0COS-7L 0.8 2.5-3.0293H,293F 2.0 1.5-2.05. 直接将复合物加入到每孔中,摇动培养板,轻轻混匀。注意:如果在无血清条件下转染,使用含血清的正常生长培养基进行细胞铺板。在加入复合物前移去生长培养基,替换为0.5ml无血清培养基

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