108CC5

8062521, Mouse x Rat Hybridoma nerve, Neuronal

• Code UNSPSC : 41106514
• Source biologique: Mouse x Rat Hybridoma nerve
• Mode de croissance: Adherent
• Caryotype: Modal No. varied with passage see reference
• Morphologie: Neuronal
• Produits: Long processes after treatment with dibutyryl cAMP, dense core vesicles, excitable membranes, neurotransmitter enzymes, synthesis of neurohormones and uptake of catecholamines.
• Récepteurs: Receptors for neurohormones: delta opioid, PGE 1 vasoactive intestinal polypeptide, adenosine, somatostatin and acetylcholine.
• Maladie(s) pertinente(s): cancer

Propriétés

• Nom du produit: 108CC5, 08062521
• Source biologique: Mouse x Rat Hybridoma nerve
• Mode de croissance: Adherent
• Caryotype: Modal No. varied with passage see reference
• Morphologie: Neuronal
• Produits: Long processes after treatment with dibutyryl cAMP, dense core vesicles, excitable membranes, neurotransmitter enzymes, synthesis of neurohormones and uptake of catecholamines.
• Récepteurs: Receptors for neurohormones: delta opioid, PGE 1 vasoactive intestinal polypeptide, adenosine, somatostatin and acetylcholine.
• Technique(s): cell culture | mammalian: suitable
• Maladie(s) pertinente(s): cancer
• Conditions d'expédition: dry ice
• Température de stockage: −196°C

Description

Origine de la lignée cellulaire

Mouse neuroblastoma x Rat glioma hybrid

Description de la lignée cellulaire

The cell line108CC5 is formed by the fusion of mouse neuroblastoma N18TG2 and rat glioma C6-BU-1using inactivated Sendai virus. This cell line was renamed NG108-5 by Klee and Nirenberg . This is a cholinergic hybrid cell line.

Application

Used as a neuronal Model

Milieu de culture

DMEM + 2 mM glutamine + 10% Foetal Bovine Serum (FBS) HAT (0.1 mM hypoxanthine, 10 μM aminopterin and 16 μM thymidine) Cells can be cultured without HAT provided they were cultured inbetween in HT medium for 3-4 days

Procédure de repiquage

Split sub-confluent cultures (70-80%) 1:3 to 1:6 i.e. seeding at 1-2x10,000 cells/cm² using 0.05% trypsin/EDTA; 5% CO₂; 37°C. The cultures rapidly produce lactic acid through anaerobic glycolysis causing the media to become acidified. The medium must never be allowed to become acidic as cells detach in clumps and take many passages to recover. Frequent inspection of cultures is therefore required.

Autres remarques

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