Fig. 4.
Fig. 4. Immunoblotting of exocytosed material. / After stimulation, the neutrophils were pelleted and the supernatant containing the exocytosed material was analyzed by SDS-PAGE and immunoblotting with anti–hCAP-18 antibodies. (A) Exocytosed material from neutrophils harvested from skin windows (107cells/mL), unstimulated cells (lane a) or cells stimulated with fMLP (lane b), IgG-coated latex beads (lane c), or ionomycin (lane d). (B) Exocytosed material from neutrophils isolated from peripheral blood (107 cells/mL), unstimulated cells (lane a) or cells stimulated with fMLP (lane b), IgG-coated latex beads (lane c), or ionomycin (lane d). (C) Exocytosed material from fMLP-stimulated neutrophils (3 × 108 cells/mL) from peripheral blood.

Immunoblotting of exocytosed material.

After stimulation, the neutrophils were pelleted and the supernatant containing the exocytosed material was analyzed by SDS-PAGE and immunoblotting with anti–hCAP-18 antibodies. (A) Exocytosed material from neutrophils harvested from skin windows (107cells/mL), unstimulated cells (lane a) or cells stimulated with fMLP (lane b), IgG-coated latex beads (lane c), or ionomycin (lane d). (B) Exocytosed material from neutrophils isolated from peripheral blood (107 cells/mL), unstimulated cells (lane a) or cells stimulated with fMLP (lane b), IgG-coated latex beads (lane c), or ionomycin (lane d). (C) Exocytosed material from fMLP-stimulated neutrophils (3 × 108 cells/mL) from peripheral blood.

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