
ab109027 stained UV-treated HeLa cells. The cells were 4% formaldehyde fixed for 10 minutes at room temperature and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1hour at room temperature to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab109027 at 1/100 dilution) overnight at +4°C. The secondary antibody (pseudo-colored green) was ab150081 used at a 1/1000 dilution for 1hour at room temperature. Alexa Fluor® 594 WGA was used to label plasma membranes (pseudo-colored red) at a 1/200 dilution for 1hour 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.
![All lanes : Anti-DDB1 antibody [EPR6089] (ab109027) at 1/50000 dilutionLane 1 : HepG2 cell lysateLane 2 : HeLa cell lysateLane 3 : NIH3T3 cell lysateLane 4 : Human platelet lysateLysates/proteins at 10 µg per lane.](http://www.bioprodhub.com/system/product_images/ab_products/2/sub_2/6926_DDB1-Primary-antibodies-ab109027-3.JPG)
All lanes : Anti-DDB1 antibody [EPR6089] (ab109027) at 1/50000 dilutionLane 1 : HepG2 cell lysateLane 2 : HeLa cell lysateLane 3 : NIH3T3 cell lysateLane 4 : Human platelet lysateLysates/proteins at 10 µg per lane.

Immunohistochemical analysis of paraffin-embedded Human breast tissue using ab109027 at a dilution of 1/100.

Equilibrium disassociation constant (KD)Learn more about KD Click here to learn more about KD