| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Carrier-Free | NBP2-35114-10ug | |||
| Carrier-Free | NBP2-35114-1mg | |||
| Carrier-Free | NBP2-35114-500ug | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-12023-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-12022-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-12011-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26630-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-54395-100ug | |||
![Immunocytochemistry /Immunofluorescence: RRM2 Antibody (SAIC-30E-7) - BSA Free [NBP3-43534] - Immunofluorescence analysis of paraformaldehyde fixed HeLa cells permeabilized with 0.15% Triton stained with NBP3-43534 (1:100 dilution) for 1h followed by Alexa Fluor 488 secondary antibody (1:1000 dilution), showing nucleoli staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP3-43534, DAPI, merged channels and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor 488 secondary antibody.](http://images.novusbio.com/fullsize/nbp3-43534_rabbit-rrm2-mab-saic-30e-7-azide-and-bsa-free-7420252214128.png "Immunocytochemistry /Immunofluorescence: RRM2 Antibody (SAIC-30E-7) - BSA Free [NBP3-43534] - Immunofluorescence analysis of paraformaldehyde fixed HeLa cells permeabilized with 0.15% Triton stained with NBP3-43534 (1:100 dilution) for 1h followed by Alexa Fluor 488 secondary antibody (1:1000 dilution), showing nucleoli staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP3-43534, DAPI, merged channels and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor 488 secondary antibody.")
![Immunocytochemistry/ Immunofluorescence: RRM2 Antibody (SAIC-30E-7) - Chimeric - BSA Free [NBP3-43533] - Immunofluorescence analysis of paraformaldehyde fixed HeLa cells permeabilized with 0.15% Triton stained with NBP3-43533 (1:100 dilution) for 1h followed by Alexa Fluor® 488 secondary antibody (1:1000 dilution), showing nucleoli staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP3-43533, DAPI, merged channels and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor® 488 secondary antibody.](http://images.novusbio.com/fullsize/nbp3-43533_mouse-rrm2-mab-saic-30e-7-chimeric-azide-and-bsa-free-immunocytochemistry-immunofluorescence-2220260325822.png "Immunocytochemistry/ Immunofluorescence: RRM2 Antibody (SAIC-30E-7) - Chimeric - BSA Free [NBP3-43533] - Immunofluorescence analysis of paraformaldehyde fixed HeLa cells permeabilized with 0.15% Triton stained with NBP3-43533 (1:100 dilution) for 1h followed by Alexa Fluor® 488 secondary antibody (1:1000 dilution), showing nucleoli staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP3-43533, DAPI, merged channels and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor® 488 secondary antibody.")
![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.")
![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.")
![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.")