A new approach to neural cell culture for long-term studies

Journal of Neuroscience Methods

Volumn 110, Issue 1-2, 2001, Pages 17-24

  Potter, Steve M ^a   DeMarse, Thomas B ^a  

^a CALIFORNIA INSTITUTE OF TECHNOLOGY   (United States)

Author keywords

Contamination; Cultured mammalian neurons; Hyperosmolality; Mold infection; Multi electrode arrays; Osmolarity; PH; Sealed culture chambers; Teflon membrane

Indexed keywords

CARBON DIOXIDE; OXYGEN; POLITEF;

AIRBORNE INFECTION; ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; CELL CULTURE; CONTROLLED STUDY; CULTURE MEDIUM; ELECTRIC ACTIVITY; ELECTRODE; ELECTROSTIMULATION; EMBRYO; EVAPORATION; FEMALE; HEALTH; HUMIDIFIER; INCUBATOR; MEMBRANE; NERVE CELL; NERVE CELL NETWORK; NONHUMAN; PRIORITY JOURNAL; RAT; STUDY; SURVIVAL TIME; TECHNIQUE; WATER PERMEABILITY; WATER VAPOR;

ANIMALS; CARBON DIOXIDE; CELL CULTURE TECHNIQUES; CELL SURVIVAL; CELLS, CULTURED; CULTURE MEDIA; ELECTROPHYSIOLOGY; EQUIPMENT CONTAMINATION; FETUS; HYDROGEN-ION CONCENTRATION; MEMBRANES, ARTIFICIAL; MICROELECTRODES; NEURONS; OSMOLAR CONCENTRATION; PERMEABILITY; RATS; TIME FACTORS;

EID: 0035975664     PISSN: 01650270     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-0270(01)00412-5     Document Type: Article

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