| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-21425-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26264-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26518-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26175-50ul | |||
![Western Blot: SCAP Antibody [NBP3-09965] - Western blot analysis of SCAP in 293T Whole Cell lysates. Antibody dilution at 1.0ug/ml](http://images.novusbio.com/fullsize/SCAP-Antibody-Western-Blot-NBP3-09965-img0001.jpg "Western Blot: SCAP Antibody [NBP3-09965] - Western blot analysis of SCAP in 293T Whole Cell lysates. Antibody dilution at 1.0ug/ml")
![Western Blot: Sulfatase-2/SULF2 Antibody [NBP3-30991] - Western blot using Novus Biologicals' antigen immunoaffinity purified anti-human Sulfatase-2/SULF2 antibody (0.15 ug/ml) on human brain lysate (20 ug/lane) and developed using goat anti rabbit HRP (1:30,000)Pierce’s Super Signal West Femto.](http://images.novusbio.com/fullsize/nbp3-30991_rabbit-sulfatase-2-sulf2-pab-811202420592135.jpg "Western Blot: Sulfatase-2/SULF2 Antibody [NBP3-30991] - Western blot using Novus Biologicals' antigen immunoaffinity purified anti-human Sulfatase-2/SULF2 antibody (0.15 ug/ml) on human brain lysate (20 ug/lane) and developed using goat anti rabbit HRP (1:30,000)Pierce’s Super Signal West Femto.")
![Immunocytochemistry/Immunofluorescence: Tyrosinase Antibody (6B2) [NBP3-26264] - Staining of MCF7 Cells with Tyrosinase Antibody (6B2) at 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeated by 0.2% Triton X-100, and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. Nuclear DNA was labeled in blue with DAPI. The secondary antibody was FITC-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26264_rabbit-tyrosinase-mab-6b2-282202412493630.jpg "Immunocytochemistry/Immunofluorescence: Tyrosinase Antibody (6B2) [NBP3-26264] - Staining of MCF7 Cells with Tyrosinase Antibody (6B2) at 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeated by 0.2% Triton X-100, and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. Nuclear DNA was labeled in blue with DAPI. The secondary antibody was FITC-conjugated Goat Anti-Rabbit IgG (H+L).")
![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: CETP Antibody (2F1) [NBP3-15191] - IHC image of CETP antibody diluted at 1:115 and staining in paraffin-embedded human liver tissue. 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 30 minutes at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.](http://images.novusbio.com/fullsize/CETP-Antibody-2F1-Immunohistochemistry-NBP3-15191-img0001.jpg "Immunohistochemistry: CETP Antibody (2F1) [NBP3-15191] - IHC image of CETP antibody diluted at 1:115 and staining in paraffin-embedded human liver tissue. 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 30 minutes at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.")
![Immunohistochemistry: LAMP-2/CD107b Antibody (23G11) [NBP3-26175] - Image of LAMP-2/CD107b Antibody (23G11) diluted at 1:100 and staining in paraffin-embedded human placenta 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 0.37% DAB.](http://images.novusbio.com/fullsize/nbp3-26175_rabbit-lamp-2-cd107b-mab-23g11-262202415475624.jpg "Immunohistochemistry: LAMP-2/CD107b Antibody (23G11) [NBP3-26175] - Image of LAMP-2/CD107b Antibody (23G11) diluted at 1:100 and staining in paraffin-embedded human placenta 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 0.37% DAB.")
![Immunohistochemistry: GRP78/HSPA5 Antibody (4H12) [NBP3-15138] - IHC image of GRP78/HSPA5 antibody diluted at 1:100 and staining in paraffin-embedded human breast cancer. 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 30 minutes 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/GRP78-HSPA5-Antibody-4H12-Immunohistochemistry-NBP3-15138-img0001.jpg "Immunohistochemistry: GRP78/HSPA5 Antibody (4H12) [NBP3-15138] - IHC image of GRP78/HSPA5 antibody diluted at 1:100 and staining in paraffin-embedded human breast cancer. 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 30 minutes 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.")