Overlay histogram showing HL60 cells stained with ab109322 (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 (ab109322, 1/100 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) (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-TNF Receptor II antibody [EPR1653] (ab109322) at 1/10000 dilutionLane 1 : Jurkat cell lysateLane 2 : MCF7 cell lysateLane 3 : SW480 cell lysateLane 4 : THP1 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_5/12762_TNF-Receptor-II-Primary-antibodies-ab109322-1.jpg)
All lanes : Anti-TNF Receptor II antibody [EPR1653] (ab109322) at 1/10000 dilutionLane 1 : Jurkat cell lysateLane 2 : MCF7 cell lysateLane 3 : SW480 cell lysateLane 4 : THP1 cell lysateLysates/proteins at 10 µg per lane.SecondaryHRP labelled goat anti-rabbit at 1/2000 dilution
ab109322, at a 1/100 dilution, staining TNF Receptor II in paraffin embedded uterus tissue by Immunohistochemistry.