| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-89980-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-11979-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-50178-0.025ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-14587-500ul | |||
![Western Blot: CLIP170 Antibody [NBP2-75095] - (1ug/ml) biotinylated staining of Human Breast Cancer lysate (35ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence, using streptavidin-HRP and using NAP blocker as a substitute for skimmed milk.](http://images.novusbio.com/fullsize/CLIP170-Antibody-Western-Blot-NBP2-75095-img0001.jpg "Western Blot: CLIP170 Antibody [NBP2-75095] - (1ug/ml) biotinylated staining of Human Breast Cancer lysate (35ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence, using streptavidin-HRP and using NAP blocker as a substitute for skimmed milk.")
![Western Blot: CD83 Antibody (JE33-61) [NBP3-32170] - Western blot analysis of CD83 on different lysates with Rabbit anti-CD83 antibody (NBP3-32170) at 1/1,000 dilution. Lane 1: Raji cell lysate Lane 2: Jurkat cell lysate Lane 3: U-937 cell lysate Lysates/proteins at 10 ug/Lane. Predicted band size: 23 kDa Observed band size: 35-45 kDa Exposure time: 2 minutes; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32170) at 1/1,000 dilution was used in 5% NFDM/TBST at 4C overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:100,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32170_rabbit-cd83-mab-je33-61-278202415295568.jpg "Western Blot: CD83 Antibody (JE33-61) [NBP3-32170] - Western blot analysis of CD83 on different lysates with Rabbit anti-CD83 antibody (NBP3-32170) at 1/1,000 dilution. Lane 1: Raji cell lysate Lane 2: Jurkat cell lysate Lane 3: U-937 cell lysate Lysates/proteins at 10 ug/Lane. Predicted band size: 23 kDa Observed band size: 35-45 kDa Exposure time: 2 minutes; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32170) at 1/1,000 dilution was used in 5% NFDM/TBST at 4C overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:100,000 dilution was used for 1 hour at room temperature.")
![Western Blot: CD83 Antibody (104) [NBP2-89980] - Lane A: Jurkat Whole Cell LysateLane B: 293T Whole Cell LysateLysates/proteins at 30 ug per lane.SecondaryGoat Anti-Rabbit IgG H&L (Dylight800) at 1/10000 dilution.Developed using the Odyssey technique. Performed under reducing conditions.Predicted band size:23 kDaObserved band size:55 kDa](http://images.novusbio.com/fullsize/CD83-Antibody-104-Western-Blot-NBP2-89980-img0001.jpg "Western Blot: CD83 Antibody (104) [NBP2-89980] - Lane A: Jurkat Whole Cell LysateLane B: 293T Whole Cell LysateLysates/proteins at 30 ug per lane.SecondaryGoat Anti-Rabbit IgG H&L (Dylight800) at 1/10000 dilution.Developed using the Odyssey technique. Performed under reducing conditions.Predicted band size:23 kDaObserved band size:55 kDa")
![Immunohistochemistry: ER alpha/NR3A1 Antibody (PD00-04) [NBP3-32321] - Immunohistochemical analysis of paraffin-embedded human cervix tissue with Rabbit anti-ER alpha/NR3A1 antibody (NBP3-32321) 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 (NBP3-32321) 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/nbp3-32321_rabbit-er-alpha-nr3a1-mab-pd00-04-298202413585568.jpg "Immunohistochemistry: ER alpha/NR3A1 Antibody (PD00-04) [NBP3-32321] - Immunohistochemical analysis of paraffin-embedded human cervix tissue with Rabbit anti-ER alpha/NR3A1 antibody (NBP3-32321) 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 (NBP3-32321) 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.")
![Flow Cytometry: CD1a Antibody (SK9) [NBP3-09148] - Analysis (surface staining) of MOLT-4 cells with anti-CD1a (SK9) purified, GAM-APC. (Compared with blank.)](http://images.novusbio.com/fullsize/CD1a-Antibody-SK9-Flow-Cytometry-NBP3-09148-img0001.jpg "Flow Cytometry: CD1a Antibody (SK9) [NBP3-09148] - Analysis (surface staining) of MOLT-4 cells with anti-CD1a (SK9) purified, GAM-APC. (Compared with blank.)")
![Immunohistochemistry-Paraffin: Estrogen Receptor Antibody (S21-V) [NBP1-30153] - human of breast tumor tissue stained with Estrogen Receptor antibody shows strong positive nuclear immunostaining.](http://images.novusbio.com/fullsize/108721_1.jpg "Immunohistochemistry-Paraffin: Estrogen Receptor Antibody (S21-V) [NBP1-30153] - human of breast tumor tissue stained with Estrogen Receptor antibody shows strong positive nuclear immunostaining.")
![Flow Cytometry: CD21 Antibody (B-E5) [NBP3-14587] - A typical staining pattern with the B-E5 monoclonal antibody of lymphocytes.](http://images.novusbio.com/fullsize/CD21-Antibody-B-E5-Flow-Cytometry-NBP3-14587-img0001.jpg "Flow Cytometry: CD21 Antibody (B-E5) [NBP3-14587] - A typical staining pattern with the B-E5 monoclonal antibody of lymphocytes.")