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RL-65

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  • 2026年03月01日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 物种来源

      大鼠

    • 是否是肿瘤细胞

      0

    • ATCC Number

      CRL-10354™

    • 年限

      5 days

    • 品系

      Sprague-Dawley

    • 运输方式

      冻存运输

    • 器官来源

    • 库存

      大量

    • 细胞形态

      上皮样

    • 生长状态

      贴壁生长

    Designations: RL-65
    Depositors:  Genentech, Inc.
    Biosafety Level: 1
    Shipped: frozen
    Medium & Serum: See Propagation
    Growth Properties: adherent
    Organism: Rattus norvegicus deposited as Rattus sp.
    Morphology: epithelial

    Source: Organ: lung
    Strain: Sprague-Dawley
    Cellular Products: cytoskeletal proteins (alpha keratin, actin, desmin, vimentin, tubulin); fibronectin; laminin
    Permits/Forms: In addition to the MTA mentioned above, other ATCC and/or regulatory permits may be required for the transfer of this ATCC material. Anyone purchasing ATCC material is ultimately responsible for obtaining the permits. Please click here for information regarding the specific requirements for shipment to your location.
    Tumorigenic: No
    Age: 5 days
    Comments: The cells exhibit different characteristic when grown with or without retinoic acid.
    In the presence of retinoic acid (50 nM), the cells resemble low non-keratinized or squamous epithelium with densely packed colonies.
    In the absence of retinoic acid, the cells form a keratinized epithelium.
    Long term cultures in the absence of retinoic acid form a stratified highly keratinized epithelium with large networks of epithelial filaments.
    The cells are maintained in a serum free medium.
    If grown in media containing serum, the properties of the cells will change.
    Propagation: ATCC complete growth medium: A 1:1 mixture of Dulbecco's modified Eagle's medium and Ham's F12 medium with 2.5 mM L-glutamine adjusted to contain 1.2 g/L sodium bicarbonate and supplemented with 0.005 mg/ml insulin, 0.01 mg/ml human transferrin, 0.1 mM ethanolamine, 0.1 mM phosphoethanolamine, 25 nM selenium, 500 nM hydrocortisone, 0.005 mM forskolin, and bovine pituitary extract (0.15 mg protein per ml).
    Temperature: 37.0°C
    Atmosphere: air, 95%; carbon dioxide (CO2), 5%
    Subculturing: Subcultivation Ratio: A subcultivation ratio of 1:10 to 1:20 is recommended
    Medium Renewal: Every 2 to 3 days
    Remove medium, add fresh 0.25% trypsin - 0.53 mM EDTA, rinse and remove trypsin. Allow the culture to sit at room temperature (or 37C) until the cells detach (about 5 minutes).
    Centrifuge, resuspend cells in fresh medium and dispense into new flasks.
    Preservation: culture medium 95%; DMSO, 5%
    Related Products: Recommended medium (without the additional supplements or serum described under ATCC Medium):ATCC 30-2006
    References: 22065: Mather JP, Roberts PE. Method of isolating lung cell line. US Patent 5,364,785 dated Nov 15 1994
    22473: Roberts PE, et al. A novel epithelial cell from neonatal rat lung: isolation and differentiated phenotype. Am. J. Physiol. 259: L415-L425, 1990. PubMed: 2260675

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    • CD65/CD65s分子

      CD65/CD65s 分子     CD65 常用单克隆抗体或代号: VIM2,HE10,CF4 主要表达细胞: PMN [M] 分子质量(kDa)和结构: 岩藻糖基神经节苷脂 功    能: 中性粒细胞活化   CD65s 常用单克隆抗体或代号: 88H7 主要表达细胞: PMN,M [M] 分子质量(kDa)和结构: Siapoly- sialyl- n

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