Overlay histogram showing HeLa cells stained with ab155103 (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 (ab155103, 1/1000 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. This antibody gave a positive signal in HeLa cells fixed with 4% paraformaldehyde (10 min)/permeabilized with 0.1% PBS-Tween for 20 min used under the same conditions.
![All lanes : Anti-Ran antibody [EPR10791(B)] (ab155103) at 1/1000 dilutionLane 1 : HepG2 cell lysateLane 2 : Lovo cell lysateLane 3 : Jurkat cell lysateLane 4 : HeLa cell lysateLane 5 : C6 cell lysateLane 6 : RAW264.7 cell lysateLane 7 : PC12 cell lysateLane 8 : NIH 3T3 cell lysateLysates/proteins at 10 µg per lane.SecondaryHRP labelled goat anti-rabbit at 1/2000 dilution](http://www.bioprodhub.com/system/product_images/ab_products/2/sub_4/20517_Ran-Primary-antibodies-ab155103-1.jpg)
All lanes : Anti-Ran antibody [EPR10791(B)] (ab155103) at 1/1000 dilutionLane 1 : HepG2 cell lysateLane 2 : Lovo cell lysateLane 3 : Jurkat cell lysateLane 4 : HeLa cell lysateLane 5 : C6 cell lysateLane 6 : RAW264.7 cell lysateLane 7 : PC12 cell lysateLane 8 : NIH 3T3 cell lysateLysates/proteins at 10 µg per lane.SecondaryHRP labelled goat anti-rabbit at 1/2000 dilution
Immunofluorescence analysis of HepG2 cells labeling Ran with ab155103 at 1/250 dilution.