Fig. 7.
Fig. 7. Anti–syntaxin 2 antibody inhibits [3H]5-HT release. / (A) The permeabilized platelet exocytosis assay was performed in the presence of increasing amounts of anti–syntaxin 2 (▪), 4 (•), and 7 (▴) antibodies and rabbit IgG (⋄ (0-0.18 mg/mL). After stimulation with Ca++ (10 μmol/L), [3H]5-HT release was measured and normalized as a percentage of control release. (B) [3H]5-HT secretion stimulated by 10 μmol/L Ca++ was analyzed in the presence of anti–syntaxin 2 antibody (20 μg/mL), anti–syntaxin 2 antibody (20 μg/mL) preincubated with His6–syntaxin 2 (0.24 mg/mL), His6–syntaxin 2 alone (0.24 mg/mL), anti–syntaxin 2 antibody (0.02 mg/mL) preincubated with His6–syntaxin 4 (0.24 mg/mL), and IgG purified from preimmune sera (20 μg/mL). The [3H]5-HT release was measured and normalized as a percentage of control release (n = 9).

Anti–syntaxin 2 antibody inhibits [3H]5-HT release.

(A) The permeabilized platelet exocytosis assay was performed in the presence of increasing amounts of anti–syntaxin 2 (▪), 4 (•), and 7 (▴) antibodies and rabbit IgG (⋄ (0-0.18 mg/mL). After stimulation with Ca++ (10 μmol/L), [3H]5-HT release was measured and normalized as a percentage of control release. (B) [3H]5-HT secretion stimulated by 10 μmol/L Ca++ was analyzed in the presence of anti–syntaxin 2 antibody (20 μg/mL), anti–syntaxin 2 antibody (20 μg/mL) preincubated with His6–syntaxin 2 (0.24 mg/mL), His6–syntaxin 2 alone (0.24 mg/mL), anti–syntaxin 2 antibody (0.02 mg/mL) preincubated with His6–syntaxin 4 (0.24 mg/mL), and IgG purified from preimmune sera (20 μg/mL). The [3H]5-HT release was measured and normalized as a percentage of control release (n = 9).

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