All lanes : Anti-Histone H2B (acetyl K20) antibody [EP859Y] - ChIP Grade (ab52988) at 1/50000 dilutionLane 1 : C6 cell lysate, untreatedLane 2 : C6 cell lysate, treated with TSALysates/proteins at 10 µg per lane.Secondarygoat anti-rabbit HRP at 1/2000 dilution
ab52988 at 1/250-1/500 dilution staining Histone H2B in human cervical carcinoma by Immunohistochemistry, Paraffin embedded tissue.
ICC/IF image of ab52988 stained HeLa cells. The cells were 4% PFA 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 (ab52988, 1/1000 dilution) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 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.
Overlay histogram showing HeLa cells stained with ab52988 (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 (ab52988, 1/100 dilution) for 30 min at 22ºC. The secondary antibody used was DyLight® 488 goat anti-rabbit IgG (H+L) (ab96899) at 1/500 dilution for 30 min at 22ºC. Isotype control antibody (black line) was rabbit IgG (monoclonal) (1µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed.
ab52988 showing positive staining in Normal tonsil tissue.
ab52988 showing positive staining in Ovarian carcinoma tissue.
ab52988 showing positive staining in Thyroid gland carcinoma tissue.
ab52988 showing positive staining in Breast carcinoma tissue.
ab52988 showing positive staining in Colonic adenocarcinoma tissue.