Culturing with trehalose produces viable endothelial cells after cryopreservation

Cryobiology

Volumn 64, Issue 3, 2012, Pages 240-244

  Campbell, Lia H ^a   Brockbank, Kelvin G M ^a,b,c  

^a Cell and Tissue Systems Inc   (United States)

^b GEORGIA INSTITUTE OF TECHNOLOGY   (United States)

^c MEDICAL UNIVERSITY OF SOUTH CAROLINA   (United States)

Author keywords

Cell culture; Cell metabolic activity; Cryopreservation; Dimethylsulfoxide; Freezing; Incubation; Proliferation; Sugar; Trehalose

Indexed keywords

BICARBONATE; BUFFER; DIMETHYL SULFOXIDE; RESAZURIN; RESORUFIN; TREHALOSE;

ANIMAL CELL; ARTICLE; CELL ACTIVITY; CELL ADHESION; CELL CULTURE; CELL METABOLISM; CELL PH; CELL PROLIFERATION; CONCENTRATION (PARAMETERS); CRYOPRESERVATION; CRYOPROTECTION; ENDOTHELIUM CELL; FLUORESCENCE ANALYSIS; FREEZING; INCUBATION TIME; NONHUMAN; PRIORITY JOURNAL; PROCESS OPTIMIZATION;

ANIMALS; CATTLE; CELL LINE; CELL PROLIFERATION; CELL SURVIVAL; CRYOPRESERVATION; CRYOPROTECTIVE AGENTS; CULTURE MEDIA; DIMETHYL SULFOXIDE; ENDOTHELIAL CELLS; FLUORESCENT DYES; FREEZING; HYDROGEN-ION CONCENTRATION; OXAZINES; SODIUM BICARBONATE; TREHALOSE; XANTHENES;

ACCIPITRIDAE; ANIMALIA; ARTEMIA; BOVINAE; TARDIGRADA;

EID: 84861229342     PISSN: 00112240     EISSN: 10902392     Source Type: Journal    
DOI: 10.1016/j.cryobiol.2012.02.006     Document Type: Article

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