Overlay histogram showing HeLa cells stained with ab109367 (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 (ab109367, 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.
All lanes : Anti-Peroxiredoxin 2 antibody [EPR5154] (ab109367) at 1/1000 dilutionLane 1 : 293T cell lysateLane 2 : HeLa cell lysateLane 3 : LnCaP cell lysateLane 4 : SH-SYSY cell lysateLysates/proteins at 10 µg per lane.SecondaryHRP labelled Goat anti-Rabbit at 1/2000 dilution
Immunofluorescent staining of Peroxiredoxin 2 in HeLa cells using ab109367 at 1/250 dilution.
Immunohistochemical analysis of Peroxiredoxin 2 in paraffin-embedded Human prostatic hyperplasia tissue using ab109367 at 1/1000 dilution.
Immunohistochemical analysis of Peroxiredoxin 2 in paraffin-embedded Human stomach tissue using ab109367 at 1/1000 dilution.
ab109367 (1/500) staining Peroxiredoxin 2 in asynchronous HeLa cells (green). Cells were fixed in methanol and counterstained with DAPI in order to highlight the nucleus (red). For further experimental details please refer to Abreview.See Abreview