| Conjugate | Catalog # | Availability | Size | Price |
|---|---|---|---|---|
| Alkaline Phosphatase | NB7365-0.5mg | |||
| FITC | NB7366 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-81104-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-11532 | |||
| Conjugate | Catalog # | Availability | Size | Price |
|---|---|---|---|---|
| Alkaline Phosphatase | NB120-5931 | |||
| Biotin | NB120-5929 | |||
| HRP | NB120-5930 | |||
| PE | NB120-5932 | |||
| Rhodamine | NB120-5928 | |||
| Conjugate | Catalog # | Availability | Size | Price |
|---|---|---|---|---|
| Biotin | NBP1-97291 | |||
| FITC | NBP1-97272 | |||
| HRP | NBP1-97296 | |||
| Rhodamine | NBP1-97271 | |||
| Texas Red | NBP1-97292 | |||
| Conjugate | Catalog # | Availability | Size | Price |
|---|---|---|---|---|
| FITC | NBP1-73836-10mg | |||
| HRP | NBP1-73839-10mg | |||
![Western Blot: Cyclin B1 Antibody (1Q3E9) [NBP3-15626] - Western blot analysis of lysates from wild type (WT) and Cyclin B1 knockout (KO) HeLa cells using [KO Validated] Cyclin B1 Rabbit mAb at 1:5000 dilution incubated at room temperature for 1.5 hours.Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25 ug per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit .Exposure time: 45s.](http://images.novusbio.com/fullsize/nbp3-15626_rabbit-cyclin-b1-mab-1q3e9-82202520986.jpg "<b>Genetic Strategies Validation. </b>Western Blot: Cyclin B1 Antibody (1Q3E9) [NBP3-15626] - Western blot analysis of lysates from wild type (WT) and Cyclin B1 knockout (KO) HeLa cells using [KO Validated] Cyclin B1 Rabbit mAb at 1:5000 dilution incubated at room temperature for 1.5 hours.Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25 ug per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit .Exposure time: 45s.")
![<b>Genetic Strategies Validation. </b>Western Blot: Cyclin B1 Antibody (1Q3E9) [Cyclin B1] - Western blot analysis of lysates from Jurkat cells using [KO Validated] Cyclin B1 Rabbit mAb at 1:5000 dilution incubated at room temperature for 1.5 hours.Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25 ug per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit .Exposure time: 45s.](http://images.novusbio.com/fullsize/nbp3-15626_rabbit-cyclin-b1-mab-1q3e9-52202517352744.jpg)
![Immunocytochemistry: L-Selectin/CD62L Antibody (IVA94) [NB500-497] - Staining of acetone/methanol fixed bovine peripheral blood (lymphocyte-enriched suspension) using anti-bovine CD62L (IVA94); secondary antibody conjugated to FITC (green), DNA stained with DAPI (blue).](http://images.novusbio.com/fullsize/L-Selectin-CD62L-Antibody-IVA94-Immunocytochemistry-NB500-497-img0001.jpg "Immunocytochemistry: L-Selectin/CD62L Antibody (IVA94) [NB500-497] - Staining of acetone/methanol fixed bovine peripheral blood (lymphocyte-enriched suspension) using anti-bovine CD62L (IVA94); secondary antibody conjugated to FITC (green), DNA stained with DAPI (blue).")
![Immunohistochemistry: CD20 Antibody (PD00-02) [NBP3-32131] - Immunohistochemical analysis of paraffin-embedded human tonsil tissue with Rabbit anti-CD20 antibody (NBP3-32131) 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 (NBP3-32131) 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/nbp3-32131_rabbit-cd20-mab-pd00-02-29820241435213.jpg "Immunohistochemistry: CD20 Antibody (PD00-02) [NBP3-32131] - Immunohistochemical analysis of paraffin-embedded human tonsil tissue with Rabbit anti-CD20 antibody (NBP3-32131) 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 (NBP3-32131) 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.")
![Western Blot: Rabbit anti-Rat IgM Heavy Chain Secondary Antibody [Alkaline Phosphatase] [NBP1-72689] - Lane 1: Rat IgG whole molecule. Lane 2: Rat IgG F(c) Fragment. Lane 3: Rat IgG Fab Fragment. Lane 4: Rat IgM Whole Molecule. Lane 5: Rat Serum. All samples were reduced. Load: 50 ng per lane. Block: incubated with blocking buffer for 30 min at RT. Primary Antibody: Anti-Rat IgM (mu chain) (RABBIT) Antibody 1:2,000 for 60 min at RT. Secondary Antibody: Anti-Rabbit IgG (GOAT) Peroxidase Conjugated Antibody 1:40,000 in incubated with blocking buffer for 30 min at RT. Predicted/Observed Size: 25 and 55 kDa for Rat IgG and Serum, 25 kDa for F(c) and Fab, 78 and 25 kDa for IgM. Rat F(c) migrates slightly higher.](http://images.novusbio.com/fullsize/Rabbit-anti-Rat-IgM-Secondary-Antibody-[Alkaline-Phosphatase]-Western-Blot-NBP1-72689-img0004.jpg "Western Blot: Rabbit anti-Rat IgM Heavy Chain Secondary Antibody [Alkaline Phosphatase] [NBP1-72689] - Lane 1: Rat IgG whole molecule. Lane 2: Rat IgG F(c) Fragment. Lane 3: Rat IgG Fab Fragment. Lane 4: Rat IgM Whole Molecule. Lane 5: Rat Serum. All samples were reduced. Load: 50 ng per lane. Block: incubated with blocking buffer for 30 min at RT. Primary Antibody: Anti-Rat IgM (mu chain) (RABBIT) Antibody 1:2,000 for 60 min at RT. Secondary Antibody: Anti-Rabbit IgG (GOAT) Peroxidase Conjugated Antibody 1:40,000 in incubated with blocking buffer for 30 min at RT. Predicted/Observed Size: 25 and 55 kDa for Rat IgG and Serum, 25 kDa for F(c) and Fab, 78 and 25 kDa for IgM. Rat F(c) migrates slightly higher.")
![Immunohistochemistry-Paraffin: CD34 Antibody (SPM610) - IHC-Prediluted [NBP2-48364] - Formalin-fixed, paraffin-embedded human Angiosarcoma stained with CD34 Monoclonal Antibody (SPM610).](http://images.novusbio.com/fullsize/CD34-Antibody-SPM610-IHC-Prediluted-Immunohistochemistry-Paraffin-NBP2-48364-img0001.jpg "Immunohistochemistry-Paraffin: CD34 Antibody (SPM610) - IHC-Prediluted [NBP2-48364] - Formalin-fixed, paraffin-embedded human Angiosarcoma stained with CD34 Monoclonal Antibody (SPM610).")
![SDS-Page: Human IgM Heavy Chain Isotype Control [NBP1-96772] - SDS PAGE Results of Human IgM Heavy Chain isotype control. Lane 1: Human IgM Heavy Chain isotype control reduced [5ug]. Lane 2: Opal Prestained Molecular Weight Marker. Lane 3: Human IgM Heavy Chain isotype control non-reduced [5ug]. 4-20% gel, Coomassie stained. Bands at expected MW.](http://images.novusbio.com/fullsize/Human-IgM-Heavy-Chain-Isotype-Control-SDS-Page-NBP1-96772-img0001.jpg "SDS-Page: Human IgM Heavy Chain Isotype Control [NBP1-96772] - SDS PAGE Results of Human IgM Heavy Chain isotype control. Lane 1: Human IgM Heavy Chain isotype control reduced [5ug]. Lane 2: Opal Prestained Molecular Weight Marker. Lane 3: Human IgM Heavy Chain isotype control non-reduced [5ug]. 4-20% gel, Coomassie stained. Bands at expected MW.")
![Flow Cytometry: Rabbit anti-Feline IgM Heavy Chain Secondary Antibody [NBP1-73920] - Phenotyping of cat blood. Cat blood cells were washed and incubated with the antibody. It was used as a secondary antibody to check for bound IgM, in cat blood. It served as a B cell marker. This image was submitted via customer review. Image using the FITC form of this antibody.](http://images.novusbio.com/fullsize/Rabbit-anti-Feline-IgM-Secondary-Antibody-[Unconjugated]-Flow-Cytometry-NBP1-73920-img0001.jpg "Flow Cytometry: Rabbit anti-Feline IgM Heavy Chain Secondary Antibody [NBP1-73920] - Phenotyping of cat blood. Cat blood cells were washed and incubated with the antibody. It was used as a secondary antibody to check for bound IgM, in cat blood. It served as a B cell marker. This image was submitted via customer review. Image using the FITC form of this antibody.")
![Western Blot: Canine IgM Isotype Control [NBP1-96787] - SDS-PAGE of Dog IgM. Lane 1: Non-Reduced Human IgG. Lane 2: 5uL OPAL Pre-stained Marker MB-210-0500. Lane 3: Reduced Dog IgM. Load: 1ug per lane. Predicted/Observed size: Non-reduced 900 kDa, Reduced at 75, 25 kDa.](http://images.novusbio.com/fullsize/Canine-IgM-Isotype-Control-Western-Blot-NBP1-96787-img0002.jpg "Western Blot: Canine IgM Isotype Control [NBP1-96787] - SDS-PAGE of Dog IgM. Lane 1: Non-Reduced Human IgG. Lane 2: 5uL OPAL Pre-stained Marker MB-210-0500. Lane 3: Reduced Dog IgM. Load: 1ug per lane. Predicted/Observed size: Non-reduced 900 kDa, Reduced at 75, 25 kDa.")
![SDS-Page: Monkey IgM Isotype Control [NBP1-97060] - Lane 1: Monkey IgM, Non-Reduced. Lane 2: Monkey IgM, Reduced. Load: 1.0 ug per lane.](http://images.novusbio.com/fullsize/Monkey-IgM-Isotype-Control-SDS-Page-NBP1-97060-img0001.jpg "SDS-Page: Monkey IgM Isotype Control [NBP1-97060] - Lane 1: Monkey IgM, Non-Reduced. Lane 2: Monkey IgM, Reduced. Load: 1.0 ug per lane.")