Figure 1. Western blot analysis of UBA2 using anti-UBA2 antibody (M03816-1). 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: human K562 whole cell lysates Lane 2: human Raji whole cell lysates Lane 3: human THP-1 whole cell lysates Lane 4: human SW579 whole cell lysates Lane 5: human HepG2 whole cell lysates Lane 6: human CCRF-CEM whole cell lysates Lane 7: rat PC-12 whole cell lysates Lane 8: mouse RAW246.7 whole cell 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 mouse anti-UBA2 antigen affinity purified monoclonal antibody (Catalog # M03816-1) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-mouse 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 # EK1001) with Tanon 5200 system. A specific band was detected for UBA2 at approximately 90KD. The expected band size for UBA2 is at 71KD.