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![ELISA: Human IL12B - Ready-To-Use ELISA Kit (Colorimetric) [NBP3-39616] - Standard Curve Reference](http://images.novusbio.com/fullsize/nbp3-39616_human-il12b-ready-to-use-elisa-kit-colorimetric-2110202415393776.png "ELISA: Human IL12B - Ready-To-Use ELISA Kit (Colorimetric) [NBP3-39616] - Standard Curve Reference")
![Sandwich ELISA: IL12B Antibody Pair [HRP] [NBP2-79527] - This standard curve is only for demonstration purposes. A standard curve should be generated for each assay.](http://images.novusbio.com/fullsize/IL12B-Antibody-Pair-[HRP]-Sandwich-ELISA-NBP2-79527-img0001.jpg "Sandwich ELISA: IL12B Antibody Pair [HRP] [NBP2-79527] - This standard curve is only for demonstration purposes. A standard curve should be generated for each assay.")
![Sandwich ELISA: SP-D Antibody Pair [HRP] [NBP2-79547] - This standard curve is only for demonstration purposes. A standard curve should be generated for each assay.](http://images.novusbio.com/fullsize/SP-D-Antibody-Pair-[HRP]-Sandwich-ELISA-NBP2-79547-img0001.jpg "Sandwich ELISA: SP-D Antibody Pair [HRP] [NBP2-79547] - This standard curve is only for demonstration purposes. A standard curve should be generated for each assay.")
![Flow Cytometry: IL12B Antibody (10B10) [NBP3-26203] - Overlay Peak curve showing A549 cells stained with IL12B Antibody (10B10) (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/nbp3-26203_rabbit-il12b-mab-10b10-28220241431278.jpg "Flow Cytometry: IL12B Antibody (10B10) [NBP3-26203] - Overlay Peak curve showing A549 cells stained with IL12B Antibody (10B10) (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.")