ICC/IF image of ab8880 stained HepG2 cells. The cells were 100% methanol fixed (5 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 (ab8880, 1/200 dilution) 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.
ab8880 staining FGF basic in Mouse olfactory epithelium tissue by Immunohistochemistry (Frozen sections). The sections were PFA-fixed prior to blocking with 1% blocking reagent from a tyramide signal amplification kit for 30 minutes at 23°C. The primary antibody was diluted 1/200 in the blocking reagent and incubated with the sample for 2 hours at 23°C. An HRP-conjugated Goat anti-Rabbit polyclonal was used as the secondary antibody, diluted 1/100. After secondary antibody incubation, the signal was amplified using a tyramide signal amplication kit with Alexa Fluor® 488 tyramide.See Abreview