Hoechst fluorescence intensity can be used to separate viable bromodeoxyuridine-labeled cells from viable non-bromodeoxyuridine-labeled cells

Cytometry

Volumn 41, Issue 2, 2000, Pages 89-95

  Mozdziak, P E ^a   Pulvermacher, P M ^b   Schultz, E ^b   Schell, K ^c  

^a NORTH CAROLINA STATE UNIVERSITY   (United States)

^b UNIVERSITY OF WISCONSIN MADISON   (United States)

^c UNIVERSITY OF WISCONSIN   (United States)

Author keywords

BrdU; Flow cytometry; Muscle; NIH 3T3 cells; Satellite cells

Indexed keywords

BROXURIDINE;

ANIMAL CELL; ARTICLE; CELL LABELING; CELL VIABILITY; CYTOMETRY; FLUORESCENCE; NONHUMAN; PRIORITY JOURNAL; SATELLITE CELL;

NASA DISCIPLINE MUSCULOSKELETAL; NON-NASA CENTER;

3T3 CELLS; ANIMAL; ANTIBODIES, MONOCLONAL; ANTIMETABOLITES; BENZIMIDAZOLES; BROMODEOXYURIDINE; CELL SEPARATION; CELL SURVIVAL; CELLS, CULTURED; DNA; FLOW CYTOMETRY; FLUORESCENT DYES; INDICATORS AND REAGENTS; INTERCALATING AGENTS; MALE; MICE; MITOSIS; MUSCLE, SKELETAL; PROPIDIUM; RATS;

EID: 0033814280     PISSN: 01964763     EISSN: None     Source Type: Journal    
DOI: 10.1002/1097-0320(20001001)41:2<89::AID-CYTO2>3.0.CO;2-I     Document Type: Article

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