WB
Western blot analysis of ADORA2B using anti-ADORA2B antibody. The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: HEK293 whole cell lysates,
Lane 2: U-87MG whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ADORA2B antigen affinity purified polyclonal antibody at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody. The signal is developed using ECL Plus Western Blotting Substrate.
ICC/IF
IF analysis of ADORA2B using anti-ADORA2B antibody.
ADORA2B was detected in an immunocytochemical section of U2OS cells. The section was incubated with rabbit anti-ADORA2B Antibody at a dilution of 1:100. Omnimabs® 488 Goat Anti-Mouse IgG(H&L) was used as secondary antibody. The section was counterstained with DAPI (Blue).
FC
Flow Cytometry analysis of U251 cells using anti-ADORA2B antibody.
Overlay histogram showing U251 cells stained with anti-ADORA2B antibody (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-ADORA2B Antibody at 1:100 dilution for 30 min at 20°C. Omnimabs® 488 Goat Anti-Mouse IgG(H&L) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG at 1:100 dilution used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.