| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-11435 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26319-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-81428-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26116-50ul | |||
![Immunohistochemistry: Glut1 Antibody (2E1) [NBP3-26319] - Image of Glut1 Antibody (2E1) diluted at 1:100 and staining in paraffin-embedded human cervical cancer 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/nbp3-26319_rabbit-glut1-mab-2e1-262202414471578.jpg "Immunohistochemistry: Glut1 Antibody (2E1) [NBP3-26319] - Image of Glut1 Antibody (2E1) diluted at 1:100 and staining in paraffin-embedded human cervical cancer 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: Glut1 Antibody (2E1) [NBP3-26319] - Image of Glut1 Antibody (2E1) diluted at 1:100 and staining in paraffin-embedded human cervical cancer 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/nbp3-26319_rabbit-glut1-mab-2e1-262202415355735.jpg)
![Immunohistochemistry-Paraffin: Vang-like Protein 2/VANGL2 Antibody [NBP1-81428] - Staining of human tonsil shows strong cytoplasmic positivity in reaction center cells.](http://images.novusbio.com/fullsize/Vang-like-Protein-2-VANGL2-Antibody-Immunohistochemistry-Paraffin-NBP1-81428-img0004.jpg "Immunohistochemistry-Paraffin: Vang-like Protein 2/VANGL2 Antibody [NBP1-81428] - Staining of human tonsil shows strong cytoplasmic positivity in reaction center cells.")
![Immunohistochemistry: Ndufs4 Antibody (9H1) [NBP3-26116] - Image of Ndufs4 Antibody (9H1) diluted at 1:100 and staining in paraffin-embedded human small intestine 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 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26116_rabbit-ndufs4-mab-9h1-27220248573312.jpg "Immunohistochemistry: Ndufs4 Antibody (9H1) [NBP3-26116] - Image of Ndufs4 Antibody (9H1) diluted at 1:100 and staining in paraffin-embedded human small intestine 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 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB.")
![Flow Cytometry: Ndufs4 Antibody (9H1) [NBP3-26116] - Overlay Peak curve showing MCF7 cells stained with Ndufs4 Antibody (9H1) (red line) at 1:100. 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/nbp3-26116_rabbit-ndufs4-mab-9h1-282202414312761.jpg)