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![Flow Cytometry: Pentraxin 3/TSG-14 Antibody (10D9) [NBP3-26356] - Overlay Peak curve showing A549 cells stained with Pentraxin 3/TSG-14 Antibody (10D9) (red line) at 1:100. The cells were incubated in 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10^6 cells) for 45min at 4C. The secondary antibody used was FITC-conjugated Goat Anti-rabbit IgG (H+L) at 1:200 dilution for 35min at 4C. Control antibody (green line) was rabbit IgG (1ug/1*10^6 cells) used under the same conditions. Acquisition of >10,000 events was performed.](http://images.novusbio.com/fullsize/nbp3-26356_rabbit-pentraxin-3-tsg-14-mab-10d9-282202414183654.jpg "Flow Cytometry: Pentraxin 3/TSG-14 Antibody (10D9) [NBP3-26356] - Overlay Peak curve showing A549 cells stained with Pentraxin 3/TSG-14 Antibody (10D9) (red line) at 1:100. The cells were incubated in 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10^6 cells) for 45min at 4C. The secondary antibody used was FITC-conjugated Goat Anti-rabbit IgG (H+L) at 1:200 dilution for 35min at 4C. Control antibody (green line) was rabbit IgG (1ug/1*10^6 cells) used under the same conditions. Acquisition of >10,000 events was performed.")
![Flow Cytometry: HLA G Antibody (17A5) [NBP3-26226] - Overlay Peak curve showing U937 cells stained with HLA G Antibody (17A5) (red line) at 1:50. The cells were fixed in 4% formaldehyde and permeated by 0.2% Triton X-100. Then 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10^6 cells) for 45min at 4C. The secondary antibody used was FITC-conjugated Goat Anti-rabbit IgG (H+L) at 1:200 dilution for 35min at 4C. Control antibody (green line) was rabbit IgG (1ug/1*10^6 cells) used under the same conditions. Acquisition of >10,000 events was performed.](http://images.novusbio.com/fullsize/nbp3-26226_rabbit-hla-g-mab-17a5-282202414183662.jpg "Flow Cytometry: HLA G Antibody (17A5) [NBP3-26226] - Overlay Peak curve showing U937 cells stained with HLA G Antibody (17A5) (red line) at 1:50. The cells were fixed in 4% formaldehyde and permeated by 0.2% Triton X-100. Then 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10^6 cells) for 45min at 4C. The secondary antibody used was FITC-conjugated Goat Anti-rabbit IgG (H+L) at 1:200 dilution for 35min at 4C. Control antibody (green line) was rabbit IgG (1ug/1*10^6 cells) used under the same conditions. Acquisition of >10,000 events was performed.")
![ELISA: CD133 Antibody (5F5) [NBP3-26366] - The Binding Activity of CD133 with CD133 Antibody. Activity: Measured by its binding ability in a functional ELISA. Immobilized CD133 at 5 ug/mL can bind CD133 Antibody, the EC50 is 0.4322-0.7189 ng/mL.](http://images.novusbio.com/fullsize/nbp3-26366_human-cd133-mab-5f5-26220241236350.jpg "ELISA: CD133 Antibody (5F5) [NBP3-26366] - The Binding Activity of CD133 with CD133 Antibody. Activity: Measured by its binding ability in a functional ELISA. Immobilized CD133 at 5 ug/mL can bind CD133 Antibody, the EC50 is 0.4322-0.7189 ng/mL.")
