SH3PX1/SNX9 expression in U2OS cells analyzed by immunofluorescence. Cells were fixed in PFA and permeabilized with 0.15% Triton. Staining was performed with Anti-SH3PX1/SNX9 Antibody (A84187) at 10µg/ml for 1 hour and Alexa Fluor 488 secondary antibody at 2µg/ml. Cytoplasmic staining shown and nuclei were stained with DAPI (blue). Negative control: Goat IgG Isotype Control at 10µg/ml followed by Alexa Fluor 488 secondary antibody at 2µg/ml.