Overlay histogram showing HeLa cells stained with ab109316 (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 (ab109316, 1/10000 dilution) for 30 min at 22°C. The secondary antibody used was Alexa Fluor® 488 goat anti-rabbit IgG (H&L) (ab150077) at 1/2000 dilution for 30 min at 22°C. Isotype control antibody (black line) was rabbit IgG (monoclonal) (0.1μg/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.
![All lanes : Anti-Zyxin antibody [EPR4302] (ab109316) at 1/10000 dilutionLane 1 : HeLa lysateLane 2 : MCF7 lysateLane 3 : C2C12 lysateLysates/proteins at 10 µg per lane.](http://www.bioprodhub.com/system/product_images/ab_products/2/sub_5/25185_Zyxin-Primary-antibodies-ab109316-1.jpg)
All lanes : Anti-Zyxin antibody [EPR4302] (ab109316) at 1/10000 dilutionLane 1 : HeLa lysateLane 2 : MCF7 lysateLane 3 : C2C12 lysateLysates/proteins at 10 µg per lane.
Immunohistochemical analysis of Zyxin in paraffin embedded Human kidney tissue, using ab109316 at a 1/250 dilution.
Immunofluorescent staining of Zyxin in HeLa cells, using ab109316 at a 1/100 dilution.