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    kdpay钱包(中国) /科研细胞 /鼠源细胞系 /其他鼠源细胞系 /EOMA(小鼠血管内皮瘤细胞)

    EOMA(小鼠血管内皮瘤细胞)

    CBP61138

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    I. General information 
    Synonyms: EOMA
    Background: The EOMA cell line was originally derived in 1980 from a mixed hemangioendothelioma arising in an adult mouse.
    Species: Mus musculus, mouse
    Tissue: tumor
    Disease: hemangioendothelioma
    Gender: adult
    Morphology: endothelial
    Growth Mode: adherent
    Doubling Time: N/A
    DNA Profile: N/A
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    Culture Medium:

    DMEM+10%FBS

    EOMA完全培养基,# CBP61138M
    We strongly suggest to purchase the complete medium from us.

    Cryopreservation medium: 90%FBS+10%DMSO
    Antigen Expression: CD31 +
    vascular addressin +
    CD45 (Ly5-T200) +
    Receptor Expression: acetylated low density liproprotein
    Ref
    Oncogene: N/A
    Genes Expressed: angiotensin converting enzyme (ACE)
    thrombospondin
    cathepsin L
    endostatin
    interleukin-6 (interleukin 6, IL-6)
    Cellular Products: angiotensin converting enzyme (ACE)
    thrombospondin
    cathepsin L
    endostatin
    interleukin-6 (interleukin 6, IL-6)
    Tumor Formation: Yes, in syngeneic mice
    Comments: The cells synthesize angiotensin-converting enzyme, express surface receptors for acetylated low density lipoprotein, produce thrombospondin and show intracellular staining with an antibody to von Willebrand factor.
    Cathepsin L is secreted by EOMA cells and is responsible for the generation of endostatin L.
    Although constitutive cytokine gene expression exists in EOMA cells, the level of IL-6 mRNA is prominently elevated by incubation with Liposome encapsulated hemoglobin (LEH).
    The cells constitutively express the vascular addressin identified by antibody MECA-99.
    EOMA cells exhibit characteristic endothelial cell properties, such as rearrangement into tubelike structures on Matrigel and retention of cobblestone morphology at confluence. They behave in vitro in a manner similar to microvascular endothelial cells.
    For more information, please contact us (4008-750-250).

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