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EOC 20

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  • 2026年03月02日
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    • 详细信息
    • 询价记录
    • 文献和实验
    • 技术资料
    • 细胞形态

      单核细胞/巨噬细胞

    • 品系

      C3H/HeJ

    • 器官来源

      大脑

    • 库存

      大量

    • ATCC Number

      CRL-2469™

    • 物种来源

      小鼠

    • 是否是肿瘤细胞

      0

    • 生长状态

      贴壁生长

    • 细胞类型

      其他细胞类型

    • 运输方式

      冻存运输

    • 年限

      10 days juvenile

    Designations: EOC 20
    Depositors:  WS Walker
    Biosafety Level: 1
    Shipped: frozen
    Medium & Serum: See Propagation
    Growth Properties: adherent
    Organism: Mus musculus deposited as mouse
    Morphology: macrophage

    Source: Organ: brain
    Strain: C3H/HeJ
    Cell Type: microglia;
    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.
    Receptors: colony stimulating factor 1 (CSF-1R, CD115)
    Antigen Expression: CD11b/CD18 (Mac-1) +, Mac-2 +, Mac-3 +, CD80 (B7-1) +, CD45 +, Ly-6C +, MHC Class I +, MHC Class II +, CD115 (colony stimulating factor 1 receptor (CSF-1R)) +, FcR +, F4/80 +/-, CD86 (B7.2) - [39974 ]
    Age: 10 days juvenile
    Gender: female
    Comments: This is an immortalized cell line derived from the brain of an apparently normal 10 day old mouse [PubMed: 8550814]. Cells were cloned in soft agar in the presence of CSF-1 and expanded on microcarrier beads. Beads were transferred to culture dishes and were subsequently passaged by scraping. The cell line is dependent on growth factor colony stimulating factor 1 (CSF-1). Conditioned medium is made from LADMAC cells (ATCC CRL-2420?) as a source of CSF-1.The cells exhibit phagocytic activity. These cells constitutively expressed high levels of major histocompatibility complex (MHC) class II antigens and expression was upregulated by recombinant murine interferon-gamma. The cells may be used to characterize the role of brain macrophages.C3H/HeJ strain is defective in TLR4 (toll-like receptor 4)
    Propagation: ATCC complete growth medium: Dulbecco's modified Eagle's medium with 4 mM L-glutamine adjusted to contain 1.5 g/L sodium bicarbonate and 4.5 g/L glucose, 70%; fetal bovine serum, 10%; LADMAC Conditioned Media (produced from the LADMAC cell line (CRL-2420), 20%
    Temperature: 37.0°C
    Subculturing: Subcultivation Ratio: A subcultivation ratio of 1:3 is recommended
    Medium Renewal: Every 2 to 3 days
    Remove 75% of the media. Scrape off the attached cells and transfer into new flasks.
    Preservation: culture medium 95%; DMSO, 5%
    Related Products: Recommended medium (without the additional supplements or serum described under ATCC Medium):ATCC 30-2002
    recommended serum:ATCC 30-2020
    purified RNA:ATCC CRL-2469R
    References: 38884: Olivas E, et al. Use of the Pannell-Milstein roller bottle apparatus to produce high concentrations of the CSF-1, the mouse macrophage growth factor. J. Immunol. Methods 182: 73-79, 1995. PubMed: 7769247
    39968: Walker WS. Establishment of mononuclear phagocyte cell lines. J. Immunol. Methods 174: 25-31, 1994. PubMed: 8083530
    39974: Walker WS, et al. Mouse microglial cell lines differing in constitutive and interferon-gamma-inducible antigen-presenting activities for naive and memory CD4+ and CD8+ T cells. J. Neuroimmunol. 63: 163-174, 1995. PubMed: 8550814
    39975: Askew D, Walker WS. Alloantigen presentation to naive CD8+ T cells by mouse microglia: evidence for a distinct phenotype based on expression of surface-associated and soluble costimulatory molecules. Glia 18: 118-128, 1996. PubMed: 8913775

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