C17.2
7062902, mouse brain, Neuronal
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About This Item
Empfohlene Produkte
product name
C17.2, 07062902
Biologische Quelle
mouse brain
Wachstumsmodus
Adherent
Karyotyp
Not specified
Morphologie
Neuronal
Produkte
Not specified
Rezeptoren
Not specified
Methode(n)
cell culture | mammalian: suitable
Versandbedingung
dry ice
Lagertemp.
−196°C
Ursprung der Zelllinie
Mouse multipotent neural progenitor or stem-like cells
Beschreibung der Zelllinie
An immortalised mouse neural progenitor cell line capable of differentiation in vitro. The cell line was established by retorviral-mediated transduction of the avian myc oncogene into mitotic progenitor cells of neonatal mouse cerrebellum. Mouse strain CD1 x C57BL/6. This cell line is a valuable tool for in vitro and in vivo studies aimed at understanding the control of cell fate and differentiation of neural progenitors. The MMLV retrovirus vector used for the immortalisation process contained a neo resistance gene transcribed from an internal SV40 promoter. Therefore the cells are neo resistant. The morphology of the cells may change over time. Cells plated at low density may tend to become more process bearing whereas those plated more densely may tend to become flat and non-process bearing.
Nährmedium
DMEM + 2 mM Glutamine + 10% Fetal Bovine Serum (FBS). Flasks should be pre-coated with poly-L-lysine at 10 μg/ml in sterile distilled water.
Subkultur-Routine
Feed cells weekly with 50% conditioned medium and 50% fresh medium or split 1:10-1:20 in fresh medium using trypsin/EDTA. 5% CO2; 37 °C. Split sub-confluent cultures 1:10 - 1:20, i.e., seeding at 2-4 x 10,000 cells/cm2. Flasks should be pre-coated with poly-L-lysine at 10 μg/ml in sterile distilled water. Cells can be split as dilute as 1:50, but the phenotype may change, i.e., cells may appear flat with an epithelial-like morphology which usually do not stain for neurofilament or GFAP.
Sonstige Hinweise
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