ICC/IF image of ab110905 stained HepG2 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 ab110905 at 10µg/ml overnight at +4°C. The secondary antibody (pseudo-colored green) was Alexa Fluor® 488 goat anti- rabbit (ab150081) IgG (H+L) preadsorbed, used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (pseudo-colored red) at a 1/200 dilution for 1h at room temperature. DAPI was used to stain the cell nuclei (pseudo-colored blue) at a concentration of 1.43µM for 1hour at room temperature.
ab110905, at a 1/50 dilution, staining CCT6A in paraffin embedded Human breast carcinoma tissue by Immunohistochemistry. The image on the right is from tissue treated with the synthesized peptide.
All lanes : Anti-CCT6A antibody (ab110905) at 1/500 dilutionLane 1 : HepG2 cell extractsLane 2 : HepG2 cell extracts with immunizing peptide at 10 µgLysates/proteins at 30 µg per lane.