WB
Western blot analysis of RPS28 using anti-RPS28 antibody. The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human Hela whole cell lysates,
Lane 2: human 293T whole cell lysates,
Lane 3: human PC-3 whole cell lysates,
Lane 4: rat spleen tissue lysates,
Lane 5: rat PC-12 whole cell lysates,
Lane 6: mouse spleen tissue lysates,
Lane 7: mouse NIH/3T3 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-RPS28 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. A specific band was detected for RPS28 at approximately 12 kDa. The expected band size for RPS28 is at 8 kDa.
IHC
IHC analysis of RPS28 using anti-RPS28 antibody.
RPS28 was detected in a paraffin-embedded section of human colon cancer tissue. The tissue section was incubated with rabbit anti-RPS28 Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.
IHC
IHC analysis of RPS28 using anti-RPS28 antibody.
RPS28 was detected in a paraffin-embedded section of human endometrial cancer tissue. The tissue section was incubated with rabbit anti-RPS28 Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.
ICC/IF
ICC/IF analysis of RPS28 using anti-RPS28 antibody and anti-Beta Tubulin antibody.
RPS28 was detected in an immunocytochemical section of Hela cells. The section was incubated with rabbit anti-RPS28 Antibody at a dilution of 1:100. Fluoro488-conjugated Anti-rabbit IgG Secondary Antibody (green)and Cy3-conjugated Anti-mouse IgG Secondary Antibody (red)were used as secondary antibody.