| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-22197-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-12016-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| IHC-Prediluted | NBP2-48448 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-20978 | |||
![ELISA: Human Hemopexin ELISA Kit (Colorimetric) [NBP2-60506]](http://images.novusbio.com/fullsize/Human-Hemopexin-ELISA-Kit-Colorimetric-ELISA-NBP2-60506-img0001.jpg "ELISA: Human Hemopexin ELISA Kit (Colorimetric) [NBP2-60506]")
![Western Blot: PDZK1 Antibody (SR2158) [NBP3-22197] - Western blot analysis using NBP3-22197 in T47-D cell lysate.](http://images.novusbio.com/fullsize/nbp3-22197_rabbit-pdzk1-mab-sr2158-57202314565420.jpg "Western Blot: PDZK1 Antibody (SR2158) [NBP3-22197] - Western blot analysis using NBP3-22197 in T47-D cell lysate.")
![Western Blot: CD31/PECAM-1 Antibody (S04-2F3) [NBP3-19533] - Western blot detection of CD31/PECAM-1 in Jurkat, 3T3 cell lysates using NBP3-19533 (1:1000 diluted). Predicted band size: 83kDa. Observed band size: 130kDa.](http://images.novusbio.com/fullsize/CD31-PECAM-1-Antibody-S04-2F3-Western-Blot-NBP3-19533-img0001.jpg "Western Blot: CD31/PECAM-1 Antibody (S04-2F3) [NBP3-19533] - Western blot detection of CD31/PECAM-1 in Jurkat, 3T3 cell lysates using NBP3-19533 (1:1000 diluted). Predicted band size: 83kDa. Observed band size: 130kDa.")
![Immunocytochemistry/Immunofluorescence: CD40 Ligand/TNFSF5 Antibody (IDEC-131 (Toralizumab)) - Chimeric [NBP3-12016] - Immunofluorescence analysis of paraformaldehyde fixed Jurkat cells on Shi-fix(TM) coverslips stained with the chimeric rabbit IgG version of IDEC-131 (Toralizumab) (NBP3-12016) at 10 ug/ml for 1h followed by Alexa Fluor(R) 488 secondary antibody (2 ug/ml), showing membrane staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP3-12016, DAPI, merged channels and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor(R) 488 secondary antibody.](http://images.novusbio.com/fullsize/CD40-Ligand-TNFSF5-Antibody-IDEC-131-Toralizumab-Chimeric-Immunocytochemistry-Immunofluorescence-NBP3-12016-img0001.jpg "Immunocytochemistry/Immunofluorescence: CD40 Ligand/TNFSF5 Antibody (IDEC-131 (Toralizumab)) - Chimeric [NBP3-12016] - Immunofluorescence analysis of paraformaldehyde fixed Jurkat cells on Shi-fix(TM) coverslips stained with the chimeric rabbit IgG version of IDEC-131 (Toralizumab) (NBP3-12016) at 10 ug/ml for 1h followed by Alexa Fluor(R) 488 secondary antibody (2 ug/ml), showing membrane staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP3-12016, DAPI, merged channels and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor(R) 488 secondary antibody.")
![Immunohistochemistry: CD34 Antibody (PDM0-12) [NBP3-32148] - Immunohistochemical analysis of paraffin-embedded human liver tissue with Mouse anti-CD34 antibody (NBP3-32148) at 1/1,000 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 (NBP3-32148) at 1/1,000 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/nbp3-32148_mouse-cd34-mab-pdm0-12-29820241426264.jpg "Immunohistochemistry: CD34 Antibody (PDM0-12) [NBP3-32148] - Immunohistochemical analysis of paraffin-embedded human liver tissue with Mouse anti-CD34 antibody (NBP3-32148) at 1/1,000 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 (NBP3-32148) at 1/1,000 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.")
