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. Author manuscript; available in PMC: 2014 May 1.
Published in final edited form as: J Immunol. 2013 Mar 29;190(9):4692–4706. doi: 10.4049/jimmunol.1202411

Fig. 2. Reduced emigration of 24p3−/− neutrophils.

Fig. 2

(A) Total cellularity of the peritoneal exudates of casein challenged mice. Cellularity was enumerated in a hemocytometer. Error bars depict SD. (B) Flow cytometry analysis of neutrophils in the peritoneal exudates. Forward and Side scatter analysis. (C & D) Peritoneal exudates were stained with Gr-1 antibody and %positive cells were determined by flow cytometry. Values are average means of triplicate experiments with 2 mice per genotype per experiment. Error bars depict SD. (E) Flow cytometry analysis of bone marrow, peripheral blood and peritoneal exudates of casein challenged mice following staining with a Gr-1 PE antibody. Values are average means of triplicate experiments with 2 mice per genotype per experiment. Error bars depict SD. (F & G). CBA analysis of inflammatory cytokines in the sera of casein challenged mice. Values are average means of triplicate experiments with 2 mice per genotype per experiment. Error bars depict SD. (H & I). Quantitative determination of chemokines MIP-2 and KC in the sera of casein challenged mice. Values are average means of triplicate experiments with 2 mice per genotype per experiment. Error bars depict SD.