| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-89570-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-89884-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-89738-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-50214-0.025ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-62564-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-11973-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide Free | NBP3-11948-25ul | |||
![Western Blot: Clusterin/APOJ Antibody (PSH04-33) [NBP3-32196] - Western blot analysis of Clusterin/APOJ on different lysates with Rabbit anti-Clusterin/APOJ antibody (NBP3-32196) at 1/2,000 dilution. Lane 1: HeLa cell lysate Lane 2: SK-Br-3 cell lysate Lane 3: A431 cell lysate Lane 4: PANC-1 cell lysate Lane 5: MCF7 cell lysate Lane 6: T-47D cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 52 kDa Observed band size: 35-80 kDa Exposure time: 1 minute 50 seconds; ECL; 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 (NBP3-32196) at 1/2,000 dilution was used in 5% NFDM/TBST at 4C overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32196_rabbit-clusterin-apoj-mab-psh04-33-27820241521244.jpg "Western Blot: Clusterin/APOJ Antibody (PSH04-33) [NBP3-32196] - Western blot analysis of Clusterin/APOJ on different lysates with Rabbit anti-Clusterin/APOJ antibody (NBP3-32196) at 1/2,000 dilution. Lane 1: HeLa cell lysate Lane 2: SK-Br-3 cell lysate Lane 3: A431 cell lysate Lane 4: PANC-1 cell lysate Lane 5: MCF7 cell lysate Lane 6: T-47D cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 52 kDa Observed band size: 35-80 kDa Exposure time: 1 minute 50 seconds; ECL; 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 (NBP3-32196) at 1/2,000 dilution was used in 5% NFDM/TBST at 4C overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: Clusterin/APOJ Antibody (PSH04-33) [NBP3-32196] - Immunohistochemical analysis of paraffin-embedded human lung cancer tissue with Rabbit anti-Clusterin/APOJ antibody (NBP3-32196) at 1/8,000 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 (NBP3-32196) at 1/8,000 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/nbp3-32196_rabbit-clusterin-apoj-mab-psh04-33-29820241492623.jpg)
![Immunohistochemistry-Paraffin: Fatty acid desaturase 2 Antibody [NBP2-82734] - IHC - Paraffin (10 ug/ml)](http://images.novusbio.com/fullsize/Fatty-acid-desaturase-2-Antibody-Immunohistochemistry-Paraffin-NBP2-82734-img0001.jpg "Immunohistochemistry-Paraffin: Fatty acid desaturase 2 Antibody [NBP2-82734] - IHC - Paraffin (10 ug/ml)")
![Immunohistochemistry-Paraffin: Fatty acid desaturase 2 Antibody [NBP2-82734] - IHC - Paraffin (10 ug/ml)](http://images.novusbio.com/fullsize/Fatty-acid-desaturase-2-Antibody-Immunohistochemistry-Paraffin-NBP2-82734-img0002.jpg)
![Western Blot: C8B Antibody [NBP2-87104] - WB Suggested Anti-C8B Antibody Titration: 0.2-1 ug/ml. Positive Control: HepG2 cell lysateC8B is supported by BioGPS gene expression data to be expressed in HepG2](http://images.novusbio.com/fullsize/C8B-Antibody-Western-Blot-NBP2-87104-img0002.jpg "Western Blot: C8B Antibody [NBP2-87104] - WB Suggested Anti-C8B Antibody Titration: 0.2-1 ug/ml. Positive Control: HepG2 cell lysateC8B is supported by BioGPS gene expression data to be expressed in HepG2")
![Immunohistochemistry: C8B Antibody [NBP2-87104] - Liver](http://images.novusbio.com/fullsize/C8B-Antibody-Immunohistochemistry-NBP2-87104-img0001.jpg)
![Western Blot: IL-18/IL-1F4 Antibody (PSH02-08) [NBP3-32451] - Western blot analysis of IL-18/IL-1F4 on different lysates with Rabbit anti-IL-18/IL-1F4 antibody (NBP3-32451) at 1/1,000 dilution. Lane 1: U-2 OS cell lysate Lane 2: A549 cell lysate Lane 3: HeLa cell lysate Lane 4: HepG2 cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 22 kDa Observed band size: 20 kDa Exposure time: 1 minute 45 seconds; 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 (NBP3-32451) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. 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/nbp3-32451_rabbit-il-18-il-1f4-mab-psh02-08-27820241633123.jpg "Western Blot: IL-18/IL-1F4 Antibody (PSH02-08) [NBP3-32451] - Western blot analysis of IL-18/IL-1F4 on different lysates with Rabbit anti-IL-18/IL-1F4 antibody (NBP3-32451) at 1/1,000 dilution. Lane 1: U-2 OS cell lysate Lane 2: A549 cell lysate Lane 3: HeLa cell lysate Lane 4: HepG2 cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 22 kDa Observed band size: 20 kDa Exposure time: 1 minute 45 seconds; 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 (NBP3-32451) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/100,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: IL-18/IL-1F4 Antibody (PSH02-08) [NBP3-32451] - Immunohistochemical analysis of paraffin-embedded human liver tissue with Rabbit anti-IL-18/IL-1F4 antibody (NBP3-32451) at 1/5,000 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 (NBP3-32451) at 1/5,000 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/nbp3-32451_rabbit-il-18-il-1f4-mab-psh02-08-298202414161830.jpg)
![Immunohistochemistry-Paraffin: TFPI Antibody (401) [NBP2-89570] - Staining of human TFPI in human kidney with rabbit monoclonal antibody (1:200).](http://images.novusbio.com/fullsize/TFPI-Antibody-401-Immunohistochemistry-Paraffin-NBP2-89570-img0001.jpg "Immunohistochemistry-Paraffin: TFPI Antibody (401) [NBP2-89570] - Staining of human TFPI in human kidney with rabbit monoclonal antibody (1:200).")
![Flow Cytometry: Clusterin/APOJ Antibody (013) [NBP2-89884] - Analysis of Human CLU on A549 cells. Cells were treated, stained with purified anti-Human CLU, then a FITC-conjugated second step antibody. The histogram were derived from gated events with the forward and side light-scatter characteristics of intact cells.](http://images.novusbio.com/fullsize/Clusterin-APOJ-Antibody-013-Flow-Cytometry-NBP2-89884-img0002.jpg "<b>Biological Strategies Validation. </b>Flow Cytometry: Clusterin/APOJ Antibody (013) [NBP2-89884] - Analysis of Human CLU on A549 cells. Cells were treated, stained with purified anti-Human CLU, then a FITC-conjugated second step antibody. The histogram were derived from gated events with the forward and side light-scatter characteristics of intact cells.")
![<b>Biological Strategies Validation. </b>Immunocytochemistry/Immunofluorescence: Clusterin/APOJ Antibody (013) [NBP2-89884] - Staining of Human CLU in Hela cells. Cells were fixed with 4% PFA, permeabilzed with 1% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP2-89884 antibody (1:60) at 37c 1 hour. Then cells were stained with the Alexa Fluor(R) 488-conjugated Goat Anti-rabbit IgG secondary antibody (green). Positive staining was localized to cytoplasm.](http://images.novusbio.com/fullsize/nbp2-89884_rabbit-monoclonal-clusterin-apoj-antibody-013-235202514371330.png)
![Western Blot: Serpin G1/C1 Inhibitor Antibody (18) [NBP2-89738] - Lane A: HepG2 Whole Cell Lysate Lysates/proteins at 30 ug per lane.Secondary Goat Anti-Rabbit IgG H&L (Dylight800) at 1/10000 dilution.Developed using the Odyssey technique. Performed under reducing conditions.Predicted band size:55 kDa Observed band size:71 kDa](http://images.novusbio.com/fullsize/Serpin-G1-C1-Inhibitor-Antibody-18-Western-Blot-NBP2-89738-img0002.jpg "Western Blot: Serpin G1/C1 Inhibitor Antibody (18) [NBP2-89738] - Lane A: HepG2 Whole Cell Lysate Lysates/proteins at 30 ug per lane.Secondary Goat Anti-Rabbit IgG H&L (Dylight800) at 1/10000 dilution.Developed using the Odyssey technique. Performed under reducing conditions.Predicted band size:55 kDa Observed band size:71 kDa")
![Immunoprecipitation: Serpin G1/C1 Inhibitor Antibody (18) [NBP2-89738] - Lane A:0.5 mg HepG2 Whole Cell Lysate 2 uL anti-SERPING1 rabbit monoclonal antibody and 15 ul of 50 % Protein G agarose. Primary antibody:Anti-SERPING1 rabbit monoclonal antibody,at 1:100 dilution Secondary antibody:Dylight 800-labeled antibody to rabbit IgG (H+L), at 1:5000 dilution Developed using the odssey technique. Performed under reducing conditions.Predicted band size: 55 kDa Observed band size: 100 kDa](http://images.novusbio.com/fullsize/Serpin-G1-C1-Inhibitor-Antibody-18-Immunoprecipitation-NBP2-89738-img0001.jpg)
![Immunohistochemistry-Paraffin: CYP4V2 Antibody (M29-P3B10) [NBP2-50214] - Immunohistochemistry was performed on formalin-fixed, paraffin-embedded normal and primary colorectal tumour tissue sections using neat culture supernatants of anti-CYP4V2 (M29-P3B10) . Photomicrographs show negative staining of anti-CYP4V2 [M29-P3B10] in normal colon mucosa and strong immunostaining in primary colorectal tumour. Cytoplasmic localisation of CYP4V2 is also observed.](http://images.novusbio.com/fullsize/antibody/CYP4V2-Antibody-M29-P3B10-Immunohistochemistry-NBP2-50214-img0004.jpg "Immunohistochemistry-Paraffin: CYP4V2 Antibody (M29-P3B10) [NBP2-50214] - Immunohistochemistry was performed on formalin-fixed, paraffin-embedded normal and primary colorectal tumour tissue sections using neat culture supernatants of anti-CYP4V2 (M29-P3B10) . Photomicrographs show negative staining of anti-CYP4V2 [M29-P3B10] in normal colon mucosa and strong immunostaining in primary colorectal tumour. Cytoplasmic localisation of CYP4V2 is also observed.")
![Immunohistochemistry: CYP4V2 Antibody (M29-P3B10) [NBP2-50214] - CYP4V2 neat supernatant.](http://images.novusbio.com/fullsize/CYP4V2-Antibody-M29-P3B10-Immunohistochemistry-NBP2-50214-img0001.jpg)
![Immunocytochemistry/Immunofluorescence: VISTA/B7-H5/PD-1H Antibody (MH5A) - Chimeric [NBP3-11973] - Immunofluorescence analysis of paraformaldehyde fixed mouse splenocytes permeabilized with 0.15% Triton and stained with the chimeric mouse IgG1 version of MH5A (NBP3-11973) 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 NBP3-11973, DAPI, merged channels and an isotype control. The isotype control was stained with an anti-unknown specificity antibody followed by Alexa Fluor(R) 488 secondary antibody.](http://images.novusbio.com/fullsize/VISTA-B7-H5-PD-1H-Antibody-MH5A-Chimeric-Immunocytochemistry-Immunofluorescence-NBP3-11973-img0001.jpg "Immunocytochemistry/Immunofluorescence: VISTA/B7-H5/PD-1H Antibody (MH5A) - Chimeric [NBP3-11973] - Immunofluorescence analysis of paraformaldehyde fixed mouse splenocytes permeabilized with 0.15% Triton and stained with the chimeric mouse IgG1 version of MH5A (NBP3-11973) 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 NBP3-11973, DAPI, merged channels and an isotype control. The isotype control was stained with an anti-unknown specificity antibody followed by Alexa Fluor(R) 488 secondary antibody.")
![ELISA: VISTA/B7-H5/PD-1H Antibody (MH5A) - Chimeric [NBP3-11973] - Binding curve of the rabbit chimeric version of the anti-VISTA antibody MH5A (NBP3-11973; blue line) to an ELISA plate coated with mouse VISTA-Fc fusion protein at a concentration of 5 ug/ml. A 3-fold serial dilution from 10000 to 1.7 ng/ml was performed using NBP3-11973. For signal detection, a 1:4000 dilution of anti-rabbit IgG1 HRP antibody was used.](http://images.novusbio.com/fullsize/VISTA-B7-H5-PD-1H-Antibody-MH5A-Chimeric-ELISA-NBP3-11973-img0002.jpg)
![Western Blot: Connexin 35/36 [p Ser 276] Antibody [NBP3-11948] - Western blot of connexin 35/36 fusion proteins showing specific immunolabeling of the ~35 kDa connexin 35/36 phosphorylated at Ser276. The first lane (1) is PKA phosphorylated protein purified from the C-Terminal domain. The second lane (2) shows phosphospecificity indicated by no labeling in protein without PKA stimulation. The third lane (3) is protein purified from the intracellular loop, demonstrating that there is no cross-reactivity with the other major PKA phosphorylation site at Ser110.](http://images.novusbio.com/fullsize/Connexin-35-36-[p-Ser-276]-Antibody-Western-Blot-NBP3-11948-img0001.jpg "Western Blot: Connexin 35/36 [p Ser 276] Antibody [NBP3-11948] - Western blot of connexin 35/36 fusion proteins showing specific immunolabeling of the ~35 kDa connexin 35/36 phosphorylated at Ser276. The first lane (1) is PKA phosphorylated protein purified from the C-Terminal domain. The second lane (2) shows phosphospecificity indicated by no labeling in protein without PKA stimulation. The third lane (3) is protein purified from the intracellular loop, demonstrating that there is no cross-reactivity with the other major PKA phosphorylation site at Ser110.")