Western blot analysis of PARK7 / DJ1 using anti-PARK7 / DJ1 antibody (A00757-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. Lane 1: rat pancreas tissue lysates, Lane 2: rat kidney tissue lysates, Lane 3: rat skeletal muscle tissue lysates, Lane 4: rat liver tissue lysates, Lane 5: rat testis tissue lysates, Lane 6: rat heart tissue lysates, Lane 7: mouse kidney tissue lysates, Lane 8: mouse skeletal muscle tissue lysates. After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PARK7 / DJ1 antigen affinity purified polyclonal antibody (Catalog # A00757-2) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PARK7 / DJ1 at approximately 22KD. The expected band size for PARK7 / DJ1 is at 20KD.