Western blot (WB): | 1:500-2000 |
Immunocytochemistry/Immunofluorescence (ICC/IF): | 1:50-400 |
Flow Cytometry (Fixed): | 1:50-200 |
Enzyme linked immunosorbent assay (ELISA): | 1:100-1000 |
Western blot analysis of EPHA2 using anti-EPHA2 antibody (A00578). 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 U-87MG whole cell lysates,
Lane 3: human SHG-44 whole cell lysates,
Lane 4: human COLO-320 whole cell lysates,
Lane 5: human SK-OV-3 whole cell lysates,
Lane 6: human A549 whole cell lysates,
Lane 7: mouse HEPA1-6 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-EPHA2 antigen affinity purified polyclonal antibody (A00578) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for EPHA2 at approximately 125 kDa. The expected band size for EPHA2 is at 108 kDa.
Flow Cytometry analysis of A549 cells using anti-EPHA2 antibody (A00578).
Overlay histogram showing A549 cells stained with A00578 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-EPHA2 Antibody (A00578) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127) 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.
IF analysis of EPHA2 using anti-EPHA2 antibody (A00578).
EPHA2 was detected in an immunocytochemical section of PC-3 cells. The section was incubated with rabbit anti-EPHA2 Antibody (A00578) at a dilution of 1:100. DyLight®488 Conjugated Goat Anti-Rabbit IgG (Green) (Catalog # BA1127) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).
Western blot analysis of EPHA2 using anti-EPHA2 antibody (A00578). 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 U-87MG whole cell lysates,
Lane 3: human SHG-44 whole cell lysates,
Lane 4: human COLO-320 whole cell lysates,
Lane 5: human SK-OV-3 whole cell lysates,
Lane 6: human A549 whole cell lysates,
Lane 7: mouse HEPA1-6 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-EPHA2 antigen affinity purified polyclonal antibody (A00578) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for EPHA2 at approximately 125 kDa. The expected band size for EPHA2 is at 108 kDa.
Flow Cytometry analysis of A549 cells using anti-EPHA2 antibody (A00578).
Overlay histogram showing A549 cells stained with A00578 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-EPHA2 Antibody (A00578) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127) 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.
IF analysis of EPHA2 using anti-EPHA2 antibody (A00578).
EPHA2 was detected in an immunocytochemical section of PC-3 cells. The section was incubated with rabbit anti-EPHA2 Antibody (A00578) at a dilution of 1:100. DyLight®488 Conjugated Goat Anti-Rabbit IgG (Green) (Catalog # BA1127) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).