C17.2

7062902, mouse brain, Neuronal

• Code UNSPSC : 41106514

Propriétés

• product name: C17.2, 07062902
• Source biologique: mouse brain
• Mode de croissance: Adherent
• Caryotype: Not specified
• Morphologie: Neuronal
• Produits: Not specified
• Récepteurs: Not specified
• Technique(s): cell culture | mammalian: suitable
• Conditions d'expédition: dry ice
• Température de stockage: −196°C

Description

Origine de la lignée cellulaire

Mouse multipotent neural progenitor or stem-like cells

Description de la lignée cellulaire

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.

Milieu de culture

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.

Procédure de repiquage

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.

Autres remarques

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