WB
Western blot analysis of ERGIC2 using anti-ERGIC2 antibody. The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human PC-3 whole cell lysates,
Lane 2: human Hela whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ERGIC2 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 ERGIC2 at approximately 45 kDa. The expected band size for ERGIC2 is at 43 kDa.
IHC
IHC analysis of ERGIC2 using anti-ERGIC2 antibody.
ERGIC2 was detected in a paraffin-embedded section of human lung cancer tissue. The tissue section was incubated with rabbit anti-ERGIC2 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 ERGIC2 using anti-ERGIC2 antibody.
ERGIC2 was detected in a paraffin-embedded section of human prostate cancer tissue. The tissue section was incubated with rabbit anti-ERGIC2 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 ERGIC2 using anti-ERGIC2 antibody and anti-Alpha Tubulin antibody.
ERGIC2 was detected in an immunocytochemical section of U2OS cells. The section was incubated with rabbit anti-ERGIC2 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.
IP
IP analysis of ERGIC2 using anti-ERGIC2 antibody in Hela whole cell lysate.
Western blot analysis of ERGIC2 using anti- ERGIC2 antibody.
Lane 1: Hela whole cell lysates(30ug),
Lane 2: Rabbit control IgG instead of anti- ERGIC2 antibody in Hela whole cell lysate,
Lane 3: anti- ERGIC2 antibody (2μg) + Hela whole cell lysate (500μg).
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti- ERGIC2 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 ERGIC2 at approximately 45 kDa. The expected band size for ERGIC2 is at 43 kDa.