| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26175-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-54338-100ug | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26518-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26192-50ul | |||
![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.")
![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)
![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.")
![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.")
![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)
![Immunocytochemistry/Immunofluorescence: Insulin R/CD220 Antibody (4B2) [NBP3-26192] - Staining of MCF7 Cells with Insulin R/CD220 Antibody (4B2) 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/nbp3-26192_rabbit-insulin-r-cd220-mab-4b2-282202412475118.jpg "Immunocytochemistry/Immunofluorescence: Insulin R/CD220 Antibody (4B2) [NBP3-26192] - Staining of MCF7 Cells with Insulin R/CD220 Antibody (4B2) 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).")