Optimisation of culture conditions for differentiation of C17.2 neural stem cells to be used for in vitro toxicity tests

Toxicology in Vitro

Volumn 27, Issue 5, 2013, Pages 1565-1569

  Lundqvist, Jessica ^a   EL Andaloussi Lilja, Johanna ^a   Svensson, Christina ^a   Gustafsson Dorfh, Helena ^a   Forsby, Anna ^a  

^a STOCKHOLM UNIVERSITY   (Sweden)

Author keywords

C17.2 cell line; Differentiation; Neural progenitor cells; Neurotrophic factors

Indexed keywords

BETA TUBULIN; BETA TUBULIN III; BIOLOGICAL MARKER; BRAIN DERIVED NEUROTROPHIC FACTOR; GLIAL FIBRILLARY ACIDIC PROTEIN; MESSENGER RNA; NERVE GROWTH FACTOR; NESTIN; ONCOPROTEIN; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; ASTROCYTE; BRAIN CELL; C17.2 CELL; CELL CLONING; CELL CULTURE; CELL DIFFERENTIATION; CELL IMMORTALIZATION; CELL LINE; CELL TYPE; CEREBELLUM; CONTROLLED STUDY; CULTURE MEDIUM; DOWN REGULATION; GLIA CELL; MONOLAYER CULTURE; NERVE CELL; NEURAL STEM CELL; NEURAL STEM CELL CULTURE; NONHUMAN; PRIMATE; PROTEIN EXPRESSION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; TOXICITY TESTING; WESTERN BLOTTING;

ANIMALS; CELL CULTURE TECHNIQUES; CELL DIFFERENTIATION; CELL LINE; MICE; NERVE TISSUE PROTEINS; NESTIN; NEURAL STEM CELLS; RNA, MESSENGER; TOXICITY TESTS; TUBULIN;

EQUIDAE;

EID: 84877805730     PISSN: 08872333     EISSN: 18793177     Source Type: Journal    
DOI: 10.1016/j.tiv.2012.04.020     Document Type: Article

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