
All lanes : Anti-Apc7 antibody (ab4171)Lane 1 : HeLa Nuclear ExtractLane 2 : HeLa Nuclear Extract with Apc7 peptide (ab13734) at 1 µg/mlLysates/proteins at 20 µg per lane.SecondaryLane 1 : Goat Anti-Rabbit IgG H&L (HRP) (ab6721) at 1/2000 dilutionLane 2 : Goat polyclonal to Rabbit IgG - H&L (HRP) (ab6721) at 1/2000 dilution

All lanes : Anti-Apc7 antibody (ab4171) at 1 µg/mlLane 1 : Heart (Mouse) Tissue LysateLane 2 : Spinal Cord (Mouse) Tissue LysateLysates/proteins at 10 µg per lane.SecondaryIRDye 680 Conjugated Goat Anti-Rabbit IgG (H+L) at 1/10000 dilutionPerformed under reducing conditions.

ICC/IF image of ab4171 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 (ab4171, 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.