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![ELISA: IL-12 ELISA Kit [Biotin] [NBP1-92677] - Standard curve](http://images.novusbio.com/fullsize/IL-12-ELISA-Kit-[Biotin]-ELISA-NBP1-92677-img0001.jpg "ELISA: IL-12 ELISA Kit [Biotin] [NBP1-92677] - Standard curve")
![ELISA: IL-21 ELISA Kit [NBP1-84816] - Standard curve](http://images.novusbio.com/fullsize/IL-21-ELISA-Kit-ELISA-NBP1-84816-img0001.jpg "ELISA: IL-21 ELISA Kit [NBP1-84816] - Standard curve")
![ELISA: Monkey IL-10 ELISA Kit (Colorimetric) [NBP1-92708]](http://images.novusbio.com/fullsize/Primate-IL-10-ELISA-Kit-Colorimetric-ELISA-NBP1-92708-img0001.jpg "ELISA: Monkey IL-10 ELISA Kit (Colorimetric) [NBP1-92708]")
![ELISA: Human OX40/TNFRSF4 ELISA Kit (Colorimetric) [NBP2-22043]](http://images.novusbio.com/fullsize/Human-OX40-TNFRSF4-ELISA-Kit-Colorimetric-ELISA-NBP2-22043-img0001.jpg "ELISA: Human OX40/TNFRSF4 ELISA Kit (Colorimetric) [NBP2-22043]")
![ELISA: Primate IL-6 ELISA Kit [NBP1-92707]](http://images.novusbio.com/fullsize/Primate-IL-6-ELISA-Kit-ELISA-NBP1-92707-img0001.jpg "ELISA: Primate IL-6 ELISA Kit [NBP1-92707]")
![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.")