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![Flow Cytometry: IL-9 Antibody (RM9A4) - Chimeric [NBP3-12023] - Mouse splenocytes were stimulated with PMA and Ionomycin in presence of Monensin for 4 hours. The cells were fixed using 2% PFA, permeabilized using 0.5% Triton and stained with anti-Fluorescein IgG antibody (4-4-20; isotype control, black line) or the rabbit IgG version of RM9A4 (NBP3-12023, pink line) at a dilution of 1:100 for 1h at RT. The blue line shows unstimulated human peripheral blood leukocytes stained with NBP3-12023. After washing, bound antibody was detected using a goat anti-mouse IgG AlexaFluor(R) 488 antibody at a dilution of 1:1000 and cells were analyzed using a FACSCanto flow-cytometer.](http://images.novusbio.com/fullsize/IL-9-Antibody-RM9A4-Chimeric-Flow-Cytometry-NBP3-12023-img0001.jpg "Flow Cytometry: IL-9 Antibody (RM9A4) - Chimeric [NBP3-12023] - Mouse splenocytes were stimulated with PMA and Ionomycin in presence of Monensin for 4 hours. The cells were fixed using 2% PFA, permeabilized using 0.5% Triton and stained with anti-Fluorescein IgG antibody (4-4-20; isotype control, black line) or the rabbit IgG version of RM9A4 (NBP3-12023, pink line) at a dilution of 1:100 for 1h at RT. The blue line shows unstimulated human peripheral blood leukocytes stained with NBP3-12023. After washing, bound antibody was detected using a goat anti-mouse IgG AlexaFluor(R) 488 antibody at a dilution of 1:1000 and cells were analyzed using a FACSCanto flow-cytometer.")
![Flow Cytometry: IL-9 Antibody (MH9A4) - Chimeric [NBP3-12022] - Human peripheral blood leukocytes were rested for 4 hours. The cells were fixed using 2% PFA, permeabilized using 0.5% Triton and stained with anti-Fluorescein IgG antibody (4-4-20; isotype control, black line) or the rabbit IgG version of MH9A4 (NBP3-12022, blue line) at a dilution of 1:100 for 1h at RT. After washing, bound antibody was detected using a goat anti-mouse IgG AlexaFluor(R) 488 antibody at a dilution of 1:1000 and cells were analyzed using a FACSCanto flow-cytometer.](http://images.novusbio.com/fullsize/IL-9-Antibody-MH9A4-Chimeric-Flow-Cytometry-NBP3-12022-img0001.jpg "Flow Cytometry: IL-9 Antibody (MH9A4) - Chimeric [NBP3-12022] - Human peripheral blood leukocytes were rested for 4 hours. The cells were fixed using 2% PFA, permeabilized using 0.5% Triton and stained with anti-Fluorescein IgG antibody (4-4-20; isotype control, black line) or the rabbit IgG version of MH9A4 (NBP3-12022, blue line) at a dilution of 1:100 for 1h at RT. After washing, bound antibody was detected using a goat anti-mouse IgG AlexaFluor(R) 488 antibody at a dilution of 1:1000 and cells were analyzed using a FACSCanto flow-cytometer.")
![ELISA: Mouse IL-12 ELISA Kit (Colorimetric) [NBP1-92658] - IL-12 ELISA Kit (Colorimetric) [NBP1-92658] - Representative standard curve for mouse IL-12 ELISA. Mouse IL- 12 was diluted in serial 2-fold steps in sample diluent. Do not use this standard curve to derive test results. A standard curve must be run for each group ofmicrowell strips assayed.](http://images.novusbio.com/fullsize/Mouse-IL-12-ELISA-Kit-Colorimetric-ELISA-NBP1-92658-img0002.jpg "ELISA: Mouse IL-12 ELISA Kit (Colorimetric) [NBP1-92658] - IL-12 ELISA Kit (Colorimetric) [NBP1-92658] - Representative standard curve for mouse IL-12 ELISA. Mouse IL- 12 was diluted in serial 2-fold steps in sample diluent. Do not use this standard curve to derive test results. A standard curve must be run for each group ofmicrowell strips assayed.")
![Mouse CCL2/MCP1 ELISA Kit [NBP1-92659] - Data for Mouse MCP-1 Platinum ELISA](http://images.novusbio.com/fullsize/Mouse-CCL2-MCP1-ELISA-Kit-NBP1-92659-img0001.jpg "Mouse CCL2/MCP1 ELISA Kit [NBP1-92659] - Data for Mouse MCP-1 Platinum ELISA")
![ELISA: TSLP ELISA Kit [DDXK-E-TSLP] - Each laboratory should establish its own standard curve. Example of standard curve using serial dilutions of TSLP (20ng/ml) prepared from supernatants of TSLP-transfected eukaryotic cells.](http://images.novusbio.com/fullsize/TSLP-ELISA-Kit-ELISA-DDXK-E-TSLP-img0001.jpg "ELISA: TSLP ELISA Kit [DDXK-E-TSLP] - Each laboratory should establish its own standard curve. Example of standard curve using serial dilutions of TSLP (20ng/ml) prepared from supernatants of TSLP-transfected eukaryotic cells.")
