Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 1:50-400 |
Flow Cytometry (Fixed): | 1:50-200 |
(Boiling the paraffin sections in 10mM citrate buffer,pH6.0,or PH8.0 EDTA repair liquid for 23 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 using anti-VEGF antibody (PB9071).The sample well of each lane was loaded with 50ug of sample under reducing conditions.Lane 1: rat lung tissue lysate,Lane 2: rat lver tissue lysate,Lane 3: rat thymus tissue lysate,Lane 4: mouse lung tissue lysate,Lane 5: mouse thymus tissue lysate,Lane 6: HEPA1-6 whole cell lysate,Lane 7: human placenta tissue lysate,Lane 8: A431 whole cell lysate,Use rabbit anti- VEGF 1:1000, 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 at approximately 27KD. The expected band size for VEGF is at 27KD.
Figure 2. IHC analysis using anti- VEGF antibody (PB9071). detected in paraffin-embedded section of human rectal cancer tissue. 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 using anti- VEGF antibody (PB9071). detected in paraffin-embedded section of human rectal cancer tissue. 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. IHC analysis using anti- VEGF antibody (PB9071). detected in paraffin-embedded section of rat brain tissue. 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 5. Flow cytometry analysis of SiHa cell HELA(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 using anti-VEGF antibody (PB9071).The sample well of each lane was loaded with 50ug of sample under reducing conditions.Lane 1: rat lung tissue lysate,Lane 2: rat lver tissue lysate,Lane 3: rat thymus tissue lysate,Lane 4: mouse lung tissue lysate,Lane 5: mouse thymus tissue lysate,Lane 6: HEPA1-6 whole cell lysate,Lane 7: human placenta tissue lysate,Lane 8: A431 whole cell lysate,Use rabbit anti- VEGF 1:1000, 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 at approximately 27KD. The expected band size for VEGF is at 27KD.
Figure 2. IHC analysis using anti- VEGF antibody (PB9071). detected in paraffin-embedded section of human rectal cancer tissue. 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 using anti- VEGF antibody (PB9071). detected in paraffin-embedded section of human rectal cancer tissue. 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. IHC analysis using anti- VEGF antibody (PB9071). detected in paraffin-embedded section of rat brain tissue. 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 5. Flow cytometry analysis of SiHa cell HELA(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).