| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26266-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26264-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26358-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26588-50ul | |||
![ELISA: Human S100B ELISA Kit (Colorimetric) [NBP2-60143] - 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/Human-S100B-ELISA-Kit-Colorimetric-ELISA-NBP2-60143-img0001.jpg "ELISA: Human S100B ELISA Kit (Colorimetric) [NBP2-60143] - These standard curves are provided for demonstration only. A standard curve should be generated for each set of samples assayed.")
![Human S100B ELISA Kit (Colorimetric) [NBP2-60143] - Standard Curve Reference](http://images.novusbio.com/fullsize/nbp2-60143_human-s100b-elisa-kit-colorimetric-3120248343413.png)
![Western Blot: Thioredoxin-1 Antibody (3H8) [NBP3-26266] - Positive Western Blot detected in: MCF-7 whole cell lysate, HepG2 whole cell lysate, A549 whole cell lysate. All lanes: Thioredoxin-1 Antibody at 1: 2000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 10, 12 kDa Observed band size: 12 kDa](http://images.novusbio.com/fullsize/nbp3-26266_rabbit-thioredoxin-1-mab-3h8-28220241140911.jpg "Western Blot: Thioredoxin-1 Antibody (3H8) [NBP3-26266] - Positive Western Blot detected in: MCF-7 whole cell lysate, HepG2 whole cell lysate, A549 whole cell lysate. All lanes: Thioredoxin-1 Antibody at 1: 2000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 10, 12 kDa Observed band size: 12 kDa")
![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: 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.")
![Western Blot: PADI4 Antibody (C12) [NBP3-41898] - Sample: Human Saliva Primary Ab: 2ug/ml NBP3-41898; Second Ab: 0.2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody](http://images.novusbio.com/fullsize/nbp3-41898_mouse-padi4-mab-c12-612202421195619.jpg "Western Blot: PADI4 Antibody (C12) [NBP3-41898] - Sample: Human Saliva Primary Ab: 2ug/ml NBP3-41898; Second Ab: 0.2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody")
![Western Blot: SHP-2/PTPN11 Antibody (7A1) [NBP3-26358] - Positive Western Blot detected in: Jurkat whole cell lysate, 293 whole cell lysate, MCF-7 whole cell lysate, Hela whole cell lysate, K562 whole cell lysate. All lanes: SHP-2/PTPN11 Antibody at 1: 2000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 69, 53 kDa Observed band size: 69 kDa](http://images.novusbio.com/fullsize/nbp3-26358_rabbit-shp-2-ptpn11-mab-7a1-282202411442626.jpg "Western Blot: SHP-2/PTPN11 Antibody (7A1) [NBP3-26358] - Positive Western Blot detected in: Jurkat whole cell lysate, 293 whole cell lysate, MCF-7 whole cell lysate, Hela whole cell lysate, K562 whole cell lysate. All lanes: SHP-2/PTPN11 Antibody at 1: 2000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 69, 53 kDa Observed band size: 69 kDa")
![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.")