Figure 1. IHC analysis of ITGA2B using anti-ITGA2B antibody (MBS1750570).
ITGA2B was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-ITGA2B Antibody (MBS1750570) overnight at 4 degree C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 degree C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) with DAB as the chromogen.
Figure 2. IHC analysis of ITGA2B using anti-ITGA2B antibody (MBS1750570).
ITGA2B was detected in paraffin-embedded section of human rectal cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-ITGA2B Antibody (MBS1750570) overnight at 4 degree C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 degree C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) with DAB as the chromogen.
Figure 3. Flow Cytometry analysis of HL-60 cells using anti-ITGA2B antibody (MBS1750570).
Overlay histogram showing HL-60 cells stained with MBS1750570 (Blue line).The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ITGA2B Antibody (MBS1750570,1ug/1x10^6 cells) for 30 min at 20 degree C. DyLight 488 conjugated goat anti-rabbit IgG (5-10ug/1x10^6 cells) was used as secondary antibody for 30 minutes at 20 degree C. Isotype control antibody (Green line) was rabbit IgG (1ug/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
Figure 4. Flow Cytometry analysis of U937 cells using anti-ITGA2B antibody (MBS1750570).
Overlay histogram showing U937 cells stained with MBS1750570 (Blue line).The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ITGA2B Antibody (MBS1750570,1ug/1x10^6 cells) for 30 min at 20 degree C. DyLight 488 conjugated goat anti-rabbit IgG (5-10ug/1x10^6 cells) was used as secondary antibody for 30 minutes at 20 degree C. Isotype control antibody (Green line) was rabbit IgG (1ug/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.