ab150363 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 ab150363 at 5µg/ml overnight at +4°C. The secondary antibody (green) was DyLight® 488 goat anti- rabbit (ab96899) 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-MAD2L1 binding protein antibody [EPR9584] (ab150363) at 1/1000 dilutionLane 1 : HepG2 cell lysateLane 2 : A431 cell lysateLane 3 : HeLa cell lysateLysates/proteins at 10 µg per lane.SecondaryHRP labelled goat anti-rabbit at 1/2000 dilution
Immunohistochemical analysis of paraffin embedded Human brain tissue labelling MAD2L1 binding protein with ab150363 antibody at a dilution of 1/100.
Immunohistochemical analysis of paraffin embedded Human cervical carcinoma tissue labelling MAD2L1 binding protein with ab150363 antibody at a dilution of 1/100.