An efficient culture method for generating large quantities of mature mouse splenic macrophages

Journal of Immunological Methods

Volumn 338, Issue 1-2, 2008, Pages 47-57

  Alatery, Attiya ^a   Basta, Sameh ^a  

^a QUEEN S UNIVERSITY   (Canada)

Author keywords

Bone marrow; Macrophages; MHC; Phagocytosis; Spleen

Indexed keywords

CD68 ANTIGEN; COLONY STIMULATING FACTOR 1; MOMA 2 PROTEIN; MONOCLONAL ANTIBODY; SIGR R1 PROTEIN; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ARTICLE; BONE MARROW CELL; CELL CULTURE; CELL DIFFERENTIATION; CELL FUNCTION; CELL ISOLATION; CELL MATURATION; CELL POPULATION; CONTROLLED STUDY; DOWN REGULATION; EMBRYO; FLOW CYTOMETRY; HUMAN; HUMAN CELL; IMMUNOFLUORESCENCE MICROSCOPY; IN VITRO STUDY; LYSOSOME; MACROPHAGE; MOUSE; NONHUMAN; PHAGOCYTOSIS; PRIORITY JOURNAL; PROTEIN EXPRESSION; SPLEEN CELL; UPREGULATION;

ANIMALS; BONE MARROW CELLS; CELL CULTURE TECHNIQUES; CULTURE MEDIA, CONDITIONED; FLOW CYTOMETRY; HUMANS; LYSOSOMES; MACROPHAGE COLONY-STIMULATING FACTOR; MACROPHAGES; MEMBRANE GLYCOPROTEINS; MICE; MICE, INBRED C57BL; PHENOTYPE; RECEPTORS, IMMUNOLOGIC; SPLEEN;

EID: 50949120645     PISSN: 00221759     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jim.2008.07.009     Document Type: Article

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