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![Fish SOD1/Cu-Zn SOD ELISA Kit (Colorimetric) [NBP3-21154] - Standard Curve Reference](http://images.novusbio.com/fullsize/nbp3-21154_sod1-cu-zn-sod-elisa-kit-colorimetric-3120248485410.png "Fish SOD1/Cu-Zn SOD ELISA Kit (Colorimetric) [NBP3-21154] - Standard Curve Reference")
![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: GADD153/CHOP Antibody (17A10) [NBP3-26630] - Overlay Peak curve showing Hela cells stained with GADD153/CHOP Antibody (17A10) (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/nbp3-26630_rabbit-gadd153-chop-mab-17a10-282202414183624.jpg "Flow Cytometry: GADD153/CHOP Antibody (17A10) [NBP3-26630] - Overlay Peak curve showing Hela cells stained with GADD153/CHOP Antibody (17A10) (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: Caspase-9 ELISA Kit [NBP1-83734] - Standard curve](http://images.novusbio.com/fullsize/Caspase-9-ELISA-Kit-ELISA-NBP1-83734-img0001.jpg "ELISA: Caspase-9 ELISA Kit [NBP1-83734] - Standard curve")
![Human p53 ELISA Kit [NBP1-91257] - Data for Human p53 Platinum ELISA](http://images.novusbio.com/fullsize/Human-p53-ELISA-Kit-NBP1-91257-img0001.jpg "Human p53 ELISA Kit [NBP1-91257] - Data for Human p53 Platinum ELISA")
