
Overlay histogram showing HepG2 cells stained with ab109221 (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 (ab109221, 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-XBP1 antibody [EPR4086] (ab109221) at 1/1000 dilutionLane 1 : Fetal heart cell lysates Lane 2 : Fetal kidney cell Fysates Lane 3 : HT-29 cell lysates Lane 4 : 293T cell lysatesLane 5 : Jurkat cell lysates Lysates/proteins at 10 µg per lane.SecondaryStandard HRP labelled goat anti-rabbit at 1/2000 dilution](http://www.bioprodhub.com/system/product_images/ab_products/2/sub_5/21816_XBP1-Primary-antibodies-ab109221-3.jpg)
All lanes : Anti-XBP1 antibody [EPR4086] (ab109221) at 1/1000 dilutionLane 1 : Fetal heart cell lysates Lane 2 : Fetal kidney cell Fysates Lane 3 : HT-29 cell lysates Lane 4 : 293T cell lysatesLane 5 : Jurkat cell lysates Lysates/proteins at 10 µg per lane.SecondaryStandard HRP labelled goat anti-rabbit at 1/2000 dilution

Immunohistochemical analysis of paraffin-embedded Human colon tissue using ab109221 at 1/500.

Immunohistochemical analysis of paraffin-embedded Human urinary bladder transitional carcinoma tissue using ab109221 at 1/500.