| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| IHC-Prediluted | NBP2-48438 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-20919 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-26963 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-20916 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-26964 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-26962 | |||
![Western Blot: CD45RC Antibody (3D3) [H00005788-M12] - Detection against Immunogen (45.54 KDa) .](http://images.novusbio.com/fullsize/CD45RC-Antibody-3D3-Western-Blot-H00005788-M12-img0001.jpg "Western Blot: CD45RC Antibody (3D3) [H00005788-M12] - Detection against Immunogen (45.54 KDa) .")
![Immunohistochemistry: Stathmin 1 Antibody (PD00-54) [NBP3-32981] - Immunohistochemical analysis of paraffin-embedded human breast cancer tissue with Rabbit anti-Stathmin 1 antibody (NBP3-32981) at 1/2,000 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (NBP3-32981) at 1/2,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.](http://images.novusbio.com/fullsize/nbp3-32981_rabbit-stathmin-1-mab-pd00-54-29820241435219.jpg "Immunohistochemistry: Stathmin 1 Antibody (PD00-54) [NBP3-32981] - Immunohistochemical analysis of paraffin-embedded human breast cancer tissue with Rabbit anti-Stathmin 1 antibody (NBP3-32981) at 1/2,000 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (NBP3-32981) at 1/2,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.")
