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![SDS-Page: Recombinant Human FABP3/H-FABP Protein [NBP3-07107] - Western blot under reducing and non-reducing conditions](http://images.novusbio.com/fullsize/Recombinant Human FABP3-H-FABP Protein-SDS-Page-NBP3-07107-img0001.jpg "SDS-Page: Recombinant Human FABP3/H-FABP Protein [NBP3-07107] - Western blot under reducing and non-reducing conditions")
![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.")
![Human IFN-omega/IFNW1 ELISA Kit [NBP1-91178] - Data for Human IFN-omega Platinum ELISA](http://images.novusbio.com/fullsize/Human-IFN-omega-IFNW1-ELISA-Kit-NBP1-91178-img0001.jpg "Human IFN-omega/IFNW1 ELISA Kit [NBP1-91178] - Data for Human IFN-omega Platinum ELISA")
![Human CD30/TNFRSF8 ELISA Kit [NBP1-91185] - Data for Human sCD30 Platinum ELISA](http://images.novusbio.com/fullsize/Human-CD30-TNFRSF8-ELISA-Kit-NBP1-91185-img0001.jpg "Human CD30/TNFRSF8 ELISA Kit [NBP1-91185] - Data for Human sCD30 Platinum ELISA")
![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]")
![Mouse ADAM33 ELISA Kit (Colorimetric) [NBP2-76998] - Standard Curve Reference](http://images.novusbio.com/fullsize/nbp2-76998_mouse-adam33-elisa-kit-colorimetric-3120248485429.png "Mouse ADAM33 ELISA Kit (Colorimetric) [NBP2-76998] - Standard Curve Reference")
![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.")