
ICC/IF image of ab109524 stained HeLa cells. The cells were 4% Formaldehyde fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab109524, 10µg/ml) overnight at +4°C. The secondary antibody (green) was ab96899, DyLight® 488 goat anti-rabbit IgG (H+L) used at a 1/250 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
![All lanes : Anti-Topoisomerase II beta antibody [EPR5377] (ab109524) at 1/50000 dilutionLane 1 : Jurkat cell lysateLane 2 : K562 cell lysateLane 3 : Raw264.7 cell lysateLane 4 : PC-12 cell lysateLysates/proteins at 10 µg per lane.](http://www.bioprodhub.com/system/product_images/ab_products/2/sub_5/13246_Topoisomerase-II-beta-Primary-antibodies-ab109524-2.jpg)
All lanes : Anti-Topoisomerase II beta antibody [EPR5377] (ab109524) at 1/50000 dilutionLane 1 : Jurkat cell lysateLane 2 : K562 cell lysateLane 3 : Raw264.7 cell lysateLane 4 : PC-12 cell lysateLysates/proteins at 10 µg per lane.

ab109524, at a 1/100 dilution, staining Human Topoisomerase II beta in breast tissue, using Immunohistochemistry, Formalin/PFA-fixed paraffin-embedded tissue.