A method for generating high-yield enriched neuronal cultures from P19 embryonal carcinoma cells

Journal of Neuroscience Methods

Volumn 204, Issue 1, 2012, Pages 87-103

  Monzo, Hector J ^a   Park, Thomas I H ^a   Montgomery, Johanna M ^a   Faull, Richard L M ^a   Dragunow, Mike ^a   Curtis, Maurice A ^a  

^a THE UNIVERSITY OF AUCKLAND   (New Zealand)

Author keywords

Mitotic inhibitor; Neurogenesis; Neuronal differentiation; Neuronal enrichment; P19 embryonal carcinoma cells; Retinoic acid

Indexed keywords

BIOLOGICAL MARKER; CALBINDIN; CALRETININ; CYTOSINE DERIVATIVE; DEOXYCYTIDINE; GLIAL FIBRILLARY ACIDIC PROTEIN; GLYCERALDEHYDE 3 PHOSPHATE DEHYDROGENASE; MATRIGEL; NESTIN; NEURON SPECIFIC NUCLEAR PROTEIN; RETINOIC ACID; SYNAPSIN I;

ANIMAL CELL; ARTICLE; CELL STRUCTURE; CELL VIABILITY; CENTRAL NERVOUS SYSTEM; CONTROLLED STUDY; EMBRYONAL CARCINOMA STEM CELL; IN VIVO STUDY; MONOLAYER CULTURE; MOUSE; NERVE CELL CULTURE; NERVE CELL DIFFERENTIATION; NERVOUS SYSTEM DEVELOPMENT; NEUROPHYSIOLOGY; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROCEDURES; PROTEIN EXPRESSION;

ANIMALS; CARCINOMA, EMBRYONAL; CELL CULTURE TECHNIQUES; CELL DIFFERENTIATION; CELL LINE; CELL LINE, TUMOR; CELL PROLIFERATION; MICE; NEUROGENESIS; NEURONS; TRETINOIN;

EID: 84855172417     PISSN: 01650270     EISSN: 1872678X     Source Type: Journal    
DOI: 10.1016/j.jneumeth.2011.11.008     Document Type: Article

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