| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Carrier-Free | NBP2-35307-10ug | |||
| Carrier-Free | NBP2-35307-1000ug | |||
| Carrier-Free | NBP2-35307-500ug | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Carrier-Free | NBP2-35228-10ug | |||
| Carrier-Free | NBP2-35228-1mg | |||
| Carrier-Free | NBP2-35228-500ug | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26518-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26588-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26331-50ul | |||
![Immunocytochemistry /Immunofluorescence: Ferritin mitochondrial Antibody (F11 (HSF102)) - BSA Free [NBP3-43584] - Immunofluorescence analysis of paraformaldehyde fixed MCF7 cells, permeabilized with 0.15% Triton, on Shi-fix coverslips stained with NBP3-43584 (1:100 dilution) for 1h followed by Alexa Fluor 488 secondary antibody (1:1000 dilution), showing cytoplasmic/mitochondrial staining. The nuclear stain is DAPI (blue). Panels show, from left-right, top-bottom, NBP3-43584, 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/nbp3-43584_rb-ferritin-mitochondrial-mab-f11-hsf102-azide-bsa-free-7420252211301.png "Immunocytochemistry /Immunofluorescence: Ferritin mitochondrial Antibody (F11 (HSF102)) - BSA Free [NBP3-43584] - Immunofluorescence analysis of paraformaldehyde fixed MCF7 cells, permeabilized with 0.15% Triton, on Shi-fix coverslips stained with NBP3-43584 (1:100 dilution) for 1h followed by Alexa Fluor 488 secondary antibody (1:1000 dilution), showing cytoplasmic/mitochondrial staining. The nuclear stain is DAPI (blue). Panels show, from left-right, top-bottom, NBP3-43584, 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: Ferritin mitochondrial Antibody (F11 (HSF102)) - BSA Free [NBP3-43584] - Paraformaldehyde fixed MCF7 cells permeabilized with 0.5% Triton were stained with anti-unknown specificity antibody (isotype control, black line) or NBP3-43584 (blue line) at a dilution of 1:100 for 1h at RT. After washing, the bound antibody was detected using a goat anti-rabbit IgG AlexaFluor 488 antibody at a dilution of 1:1000, and the cells were analyzed using a FACSCanto flow-cytometer.](http://images.novusbio.com/fullsize/nbp3-43584_rb-ferritin-mitochondrial-mab-f11-hsf102-azide-bsa-free-74202522113039.png)
![SDS-Page: Primate IL-1 beta/IL-1F2 Protein [NBP2-35307]](http://images.novusbio.com/fullsize/Primate-IL-1-beta-IL-1F2-Protein-SDS-Page-NBP2-35307-img0001.jpg "SDS-Page: Primate IL-1 beta/IL-1F2 Protein [NBP2-35307]")
![SDS-Page: Porcine IL-1 beta/IL-1F2 Protein [NBP2-35228]](http://images.novusbio.com/fullsize/Porcine-IL-1-beta-IL-1F2-Protein-SDS-Page-NBP2-35228-img0001.jpg "SDS-Page: Porcine IL-1 beta/IL-1F2 Protein [NBP2-35228]")
![Immunohistochemistry: Serpin A8/Angiotensinogen Antibody (8A9) [NBP3-26518] - Image of Serpin A8/Angiotensinogen Antibody (8A9) diluted at 1:100 and staining in paraffin-embedded human kidney tissue performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26518_rabbit-serpin-a8-angiotensinogen-mab-8a9-26220241535574.jpg "Immunohistochemistry: Serpin A8/Angiotensinogen Antibody (8A9) [NBP3-26518] - Image of Serpin A8/Angiotensinogen Antibody (8A9) diluted at 1:100 and staining in paraffin-embedded human kidney tissue performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.")
![Immunohistochemistry: FBPase 1 Antibody (4G3) [NBP3-26588] - Image of FBPase 1 Antibody (4G3) diluted at 1:100 and staining in paraffin-embedded human pancreatic tissue performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26588_rabbit-fbpase-1-mab-4g3-262202414471585.jpg "Immunohistochemistry: FBPase 1 Antibody (4G3) [NBP3-26588] - Image of FBPase 1 Antibody (4G3) diluted at 1:100 and staining in paraffin-embedded human pancreatic tissue performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.")
![Immunohistochemistry: PSGL-1/CD162 Antibody (3G11) [NBP3-26331] - Image of PSGL-1/CD162 Antibody (3G11) diluted at 1:100 and staining in paraffin-embedded human tonsil tissue performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26331_rabbit-psgl-1-cd162-mab-3g11-262202415355725.jpg "Immunohistochemistry: PSGL-1/CD162 Antibody (3G11) [NBP3-26331] - Image of PSGL-1/CD162 Antibody (3G11) diluted at 1:100 and staining in paraffin-embedded human tonsil tissue performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.")
![ELISA: Rabbit C-Peptide ELISA Kit (Colorimetric) [NBP2-59959] - These standard curves are provided for demonstration only. A standard curve should be generated for each set of samples assayed.](http://images.novusbio.com/fullsize/Rabbit-C-Peptide-ELISA-Kit-Colorimetric-ELISA-NBP2-59959-img0001.jpg "ELISA: Rabbit C-Peptide ELISA Kit (Colorimetric) [NBP2-59959] - These standard curves are provided for demonstration only. A standard curve should be generated for each set of samples assayed.")
![Rabbit C-Peptide ELISA Kit (Colorimetric) [NBP2-59959] - Standard Curve Reference](http://images.novusbio.com/fullsize/nbp2-59959_rabbit-c-peptide-elisa-kit-colorimetric-3120248504626.png)