Overlay histogram showing SH-SH5Y cells stained with ab85788 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab85788, 1μg/1x106 cells) for 30 min at 22°C. The secondary antibody used was Alexa Fluor® 488 goat anti-mouse IgG (H&L) (ab150113) at 1/2000 dilution for 30 min at 22°C. Isotype control antibody (black line) was mouse IgG1 [ICIGG1] (ab91353, 1μg/1x106 cells) used under the same conditions. Unlabelled sample (blue line) was also used as a control. Acquisition of >5,000 events were collected using a 20mW Argon ion laser (488nm) and 525/30 bandpass filter. This antibody gave a positive signal in SH-SY5Y cells fixed with 4% paraformaldehyde (10 min)/permeabilized with 0.1% PBS-Tween for 20 min used under the same conditions.
All lanes : Anti-CACNB4 antibody [S10-7] (ab85788) at 1 µg/mlLane 1 : Molecular weight markerLane 2 : Lysates prepared from CHO-T cells transfected with CACNB4 gene
ab85788 staining CACNB4 in human hippocapmpus tissue section by IHC-P. Bouin's fixed and paraffin-embedded tissue sections were used.
Anti-CACNB4 antibody [S10-7] (ab85788) at 1/1000 dilutiondeveloped using the ECL techniquePerformed under reducing conditions.