| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26145-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26347-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26543-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26684-50ul | |||
![ELISA: Mer Antibody (8H11) [NBP3-26145] - The Binding Activity of Mer with anti-Mer Antibody. Activity: Measured by its binding ability in a functional ELISA. Immobilized Mer at 2 ug/mL can bind Mer Antibody, the EC50 is 41.31-72.08 ng/mL.](http://images.novusbio.com/fullsize/nbp3-26145_human-mer-mab-8h11-26220241227237.jpg "ELISA: Mer Antibody (8H11) [NBP3-26145] - The Binding Activity of Mer with anti-Mer Antibody. Activity: Measured by its binding ability in a functional ELISA. Immobilized Mer at 2 ug/mL can bind Mer Antibody, the EC50 is 41.31-72.08 ng/mL.")
![Flow Cytometry: Ret Antibody (8D12) [NBP3-26347] - Overlay histogram showing Hela cells stained with Ret Antibody (8D12) (red line) at 1:50. 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 1 h at 4C. The secondary antibody used was FITC-conjugated goat anti-rabbit IgG (H+L) at 1/200 dilution for 30min 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/nbp3-26347_rabbit-ret-mab-8d12-282202414183622.jpg "Flow Cytometry: Ret Antibody (8D12) [NBP3-26347] - Overlay histogram showing Hela cells stained with Ret Antibody (8D12) (red line) at 1:50. 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 1 h at 4C. The secondary antibody used was FITC-conjugated goat anti-rabbit IgG (H+L) at 1/200 dilution for 30min 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: NMDAR1 Antibody (24F5) [NBP3-26543] - Overlay Peak curve showing SH-SY5Y cells stained with NMDAR1 Antibody (24F5) (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/nbp3-26543_rabbit-nmdar1-mab-24f5-282202414312771.jpg "Flow Cytometry: NMDAR1 Antibody (24F5) [NBP3-26543] - Overlay Peak curve showing SH-SY5Y cells stained with NMDAR1 Antibody (24F5) (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.")
![Flow Cytometry: CD3 zeta Antibody (21H6) [NBP3-26684] - Overlay Peak curve showing Jurkat cells stained with CD3 zeta Antibody (21H6) (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/nbp3-26684_rabbit-cd3-zeta-mab-21h6-282202414312735.jpg "Flow Cytometry: CD3 zeta Antibody (21H6) [NBP3-26684] - Overlay Peak curve showing Jurkat cells stained with CD3 zeta Antibody (21H6) (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.")
