宁波泰斯拓生物

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EOC 2

货号 TS212201
中文名称 null
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产品简介
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产品名称: EOC 2
商品货号: TS212201
Organism: Mus musculus, mouse
Tissue:
brain
Cell Type: microglia
Product Format: frozen
Morphology: macrophage
Culture Properties: adherent
Biosafety Level: 1

Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country.

Age: 10 days
Gender: female
Strain: C3H/HeJ
Applications:
The cells may be used to characterize the role of brain macrophages.
Storage Conditions: liquid nitrogen vapor phase
Images:
Derivation:
This is an immortalized cell line derived from the brain of an apparently normal 10 day old mouse.
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.
Clinical Data:
female
10 days
Antigen Expression:
CD11b/CD18 (Mac-1) +, Mac-2 +, Mac-3 +, CD80 (B7-1) +, CD86 (B7.2) +; CD45 +, Ly-6C +, F4/80 +, MHC Class I +, MHC Class II +, CD115 (colony stimulating factor 1 receptor (CSF-1R)) +, FcR +
Receptor Expression:
colony stimulating factor 1 (CSF-1R, CD115)
Genes Expressed:
CD11b/CD18 (Mac-1) +, Mac-2 +, Mac-3 +, CD80 (B7-1) +, CD86 (B7.2) +; CD45 +, Ly-6C +, F4/80 +, MHC Class I +, MHC Class II +, CD115 (colony stimulating factor 1 receptor (CSF-1R)) +, FcR +
Comments:
The cell line is dependent on colony stimulating factor 1 (CSF-1).
The cells exhibit phagocytic activity.

Unlike EOC 13.31 (ATCC CRL-2468) and EOC 20 (ATCC CRL-2469), these cells do not constitutively express high levels of major histocompatibility complex (MHC) class II antigens and expression is not upregulated by recombinant murine interferon-gamma.

C3H/HeJ strain is defective in TLR4 (toll-like receptor 4)

Complete Growth Medium: Dulbeccos modified Eagles 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%
Subculturing:
  1. Remove and discard 75% of the media.
  2. Scrape off the attached cells with a cell scraper.
  3. Add appropriate aliquots of cell suspension to new culture vessels.
  4. Incubate cultures at 37°C.

    Subcultivation Ratio: 1:2 to 1:4
    Medium Renewal: Every 2 to 3 days
    Cryopreservation:
    Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO
    Storage temperature: liquid nitrogen vapor phase
    Culture Conditions:
    Temperature: 37°C
    Name of Depositor: WS Walker
    Deposited As: mouse
    References:

    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

    Walker WS. Establishment of mononuclear phagocyte cell lines. J. Immunol. Methods 174: 25-31, 1994. PubMed: 8083530

    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

    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