WB
Western blot analysis of VE-Cadherin/CDH5 using anti-VE-Cadherin/CDH5 antibody. The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-VE-Cadherin/CDH5 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.
IHC
IHC analysis of VE-Cadherin/CDH5 using anti-VE-Cadherin/CDH5 antibody.
VE-Cadherin/CDH5 was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. The tissue section was incubated with rabbit anti-VE-Cadherin/CDH5 Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.
IF-P
IF analysis of VE-Cadherin/CDH5 using anti-VE-Cadherin/CDH5 antibody.
VE-Cadherin/CDH5 was detected in a paraffin-embedded section of human lung cancer tissue. The tissue section was incubated with rabbit anti-VE-Cadherin/CDH5 Antibody at a dilution of 1:100. Cy3-conjugated Anti-rabbit IgG Secondary Antibody (red) was used as secondary antibody. The section was counterstained with DAPI (Blue).
FC
Flow Cytometry analysis of HepG2 cells using anti-VE-Cadherin/CDH5 antibody.
Overlay histogram showing HepG2 cells stained with Rabbit polyclonal antibody to VE-Cadherin/CDH5(Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-VE-Cadherin/CDH5 Antibody at 1:100 dilution for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG 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 (Red line) was also used as a control.