Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 1:50-400 |
Immunocytochemistry/Immunofluorescence (ICC/IF): | 1:50-400 |
Flow Cytometry (Fixed): | 1:50-200 |
ELISA(Cap): | 1:50-1:200 |
(Boiling the paraffin sections in 10mM citrate buffer,pH6.0,or PH8.0 EDTA repair liquid for 20 mins is required for the staining of formalin/paraffin sections.) Optimal working dilutions must be determined by end user. |
Figure 1. Western blot analysis of VEGF Receptor 2 using anti-VEGF Receptor 2 antibody (A00901-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. Lane 1: Recombinant mouse VEGFR2 Protein 1ng. anti-VEGF Receptor 2 antigen affinity purified polyclonal antibody (Catalog # A00901-3)probed with a goat anti-rabbit IgG-HRP secondary antibody The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) . A specific band was detected for VEGF Receptor 2 at approximately 180-250KD. The expected band size for VEGF Receptor 2 is at 150KD.
Figure 2. IHC analysis of VEGF Receptor 2 using anti-VEGF Receptor 2 antibody (A00901-3).VEGF Receptor 2 was detected in paraffin-embedded section of mouse kidney tissue. anti-VEGF Receptor 2 Antibody (A00901-3) . Biotinylated goat anti-rabbit IgG was used as secondary antibody . The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
Figure 3. IHC analysis of VEGF Receptor 2 using anti-VEGF Receptor 2 antibody (A00901-3).VEGF Receptor 2 was detected in paraffin-embedded section of rat kidney tissue. anti-VEGF Receptor 2 Antibody (A00901-3) . Biotinylated goat anti-rabbit IgG was used as secondary antibody . The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
Figure 4. ICC analysis of anti- KDR antibody (A00901-3).was detected in immunocytochemical section of NIH/3T3 cells. Cells were stained using the Dylight594-conjugated Anti-rabbit IgG Secondary Antibody (red)(Catalog?#?BA1142) and counterstained with DAPI (blue)
Figure 5. Flow cytometry analysis of LLC cell (1:100) DyLight 488 conjugated goat anti- rabbit IgG(blue) was used as secondary antibody. Isotype control antibody (Green line) was rabbit IgG DyLight 488. Unlabelled sample (Red line).
Figure 6. Flow cytometry analysis of MFC cell (1:100) DyLight 488 conjugated goat anti- rabbit IgG(blue) was used as secondary antibody. Isotype control antibody (Green line) was rabbit IgG DyLight 488. Unlabelled sample (Red line).
Figure 1. Western blot analysis of VEGF Receptor 2 using anti-VEGF Receptor 2 antibody (A00901-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. Lane 1: Recombinant mouse VEGFR2 Protein 1ng. anti-VEGF Receptor 2 antigen affinity purified polyclonal antibody (Catalog # A00901-3)probed with a goat anti-rabbit IgG-HRP secondary antibody The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) . A specific band was detected for VEGF Receptor 2 at approximately 180-250KD. The expected band size for VEGF Receptor 2 is at 150KD.
Figure 2. IHC analysis of VEGF Receptor 2 using anti-VEGF Receptor 2 antibody (A00901-3).VEGF Receptor 2 was detected in paraffin-embedded section of mouse kidney tissue. anti-VEGF Receptor 2 Antibody (A00901-3) . Biotinylated goat anti-rabbit IgG was used as secondary antibody . The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
Figure 3. IHC analysis of VEGF Receptor 2 using anti-VEGF Receptor 2 antibody (A00901-3).VEGF Receptor 2 was detected in paraffin-embedded section of rat kidney tissue. anti-VEGF Receptor 2 Antibody (A00901-3) . Biotinylated goat anti-rabbit IgG was used as secondary antibody . The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
Figure 4. ICC analysis of anti- KDR antibody (A00901-3).was detected in immunocytochemical section of NIH/3T3 cells. Cells were stained using the Dylight594-conjugated Anti-rabbit IgG Secondary Antibody (red)(Catalog?#?BA1142) and counterstained with DAPI (blue)
Figure 5. Flow cytometry analysis of LLC cell (1:100) DyLight 488 conjugated goat anti- rabbit IgG(blue) was used as secondary antibody. Isotype control antibody (Green line) was rabbit IgG DyLight 488. Unlabelled sample (Red line).
Figure 6. Flow cytometry analysis of MFC cell (1:100) DyLight 488 conjugated goat anti- rabbit IgG(blue) was used as secondary antibody. Isotype control antibody (Green line) was rabbit IgG DyLight 488. Unlabelled sample (Red line).