RAW 264 Cell Line from mouse
85062803, mouse blood, Macrophage
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RAW 264 Cell Line from mouse, 85062803
Biologische Quelle
mouse blood
Beschreibung
Mouse leukemic monocyte-macrophage
Wachstumsmodus
Semi-adherent
Karyotyp
Not specified
Morphologie
Macrophage
Produkte
Lysozyme
Rezeptoren
Immunoglobulin and complement
Methode(n)
cell culture | mammalian: suitable
Relevante Krankheit(en)
cancer
Versandbedingung
dry ice
Lagertemp.
−196°C
Ursprung der Zelllinie
Mouse leukaemic monocyte-macrophage
Beschreibung der Zelllinie
Established from an ascites of a tumour induced in a male mouse by intraperitoneal injection of Abselon Leukaemia virus (A-MuLV). Cells with pinocytose neutral red and phagocytose zymosan. Cells capable of antibody-dependent lysis of sheep erythrocytes and tumour targets. Growth inhibited by LPS (0.5ng/ml).
Anwendung
RAW 264 Cell Line from mouse has been used:
- to study the anti-inflammatory effect of galectin-3 on RAW 264 macrophages which are stimulated with lipopolysaccharide
- to study the effect of titanium particles on progranulin (PGRN) expression in RAW 264 cells
- to study the effects of a nutritional supplement on interferon-γ (IFN-γ)-induced expression of macrophage chemoattractant protein-1 (MCP-1) and intercellular adhesion molecule-1 (ICAM-1)
Nährmedium
EMEM (EBSS) + 2mM Glutamine + 1% Non Essential Amino Acids (NEAA) + 10% Foetal Bovine Serum (FBS) or DMEM + 2mM Glutamine + 10% Foetal Bovine Serum (FBS).
Subkultur-Routine
Split sub-confluent cultures (70-80%) 1:3 to 1:6 i.e. seeding at 2-4x10,000 cells/cm2; 5% CO2; 37°C. Remove the cells mechanically. Cells are semi-adherent, i.e. some cells grows in suspension, some loosely attach to the surface and others flattened out and attach to the flask. Cells should not be allowed to overgrow and become confluent as this can lead to loss of the flattened adherent cell characteristic.
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