| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-19249-0.1mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB100-56436SS | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| IHC-Prediluted | NBP2-48026 | |||
| Azide and BSA Free | NBP3-11568 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-33140 | |||
| IHC-Prediluted | NBP2-44646 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-54344-100ug | |||
![Flow Cytometry: CD74 Antibody (CerCLIP.1) [NBP1-19249] - A cell surface stain was performed on Daudi cells with CD74 Antibody (CerCLIP.1) NBP1-19249AF647 (blue) and a matched isotype control NBP2-27287AF647 (orange). Cells were incubated in an antibody dilution of 2 ug/mL for 20 minutes at room temperature. Both antibodies were conjugated to Alexa Fluor 647.](http://images.novusbio.com/fullsize/CD74-Antibody-CerCLIP-1-Flow-Cytometry-NBP1-19249-img0001.jpg "Flow Cytometry: CD74 Antibody (CerCLIP.1) [NBP1-19249] - A cell surface stain was performed on Daudi cells with CD74 Antibody (CerCLIP.1) NBP1-19249AF647 (blue) and a matched isotype control NBP2-27287AF647 (orange). Cells were incubated in an antibody dilution of 2 ug/mL for 20 minutes at room temperature. Both antibodies were conjugated to Alexa Fluor 647.")
![Western Blot: Carboxylesterase 1/CES1 Antibody (JE33-04) [NBP3-32541] - Western blot analysis of Carboxylesterase 1/CES1 on different lysates with Rabbit anti-Carboxylesterase 1/CES1 antibody (NBP3-32541) at 1/1,000 dilution. Lane 1: U-937 cell lysate (20 ug/Lane) Lane 2: Human liver tissue lysate (10 ug/Lane) Lane 3: Human lung tissue lysate (10 ug/Lane) Predicted band size: 62.5 kDa Observed band size: 55 kDa Exposure time: 16 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 (NBP3-32541) 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/nbp3-32541_rabbit-carboxylesterase-1-ces1-mab-je33-04-278202416331252.jpg "Western Blot: Carboxylesterase 1/CES1 Antibody (JE33-04) [NBP3-32541] - Western blot analysis of Carboxylesterase 1/CES1 on different lysates with Rabbit anti-Carboxylesterase 1/CES1 antibody (NBP3-32541) at 1/1,000 dilution. Lane 1: U-937 cell lysate (20 ug/Lane) Lane 2: Human liver tissue lysate (10 ug/Lane) Lane 3: Human lung tissue lysate (10 ug/Lane) Predicted band size: 62.5 kDa Observed band size: 55 kDa Exposure time: 16 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 (NBP3-32541) 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: Carboxylesterase 1/CES1 Antibody (JE33-04) [NBP3-32541] - Immunohistochemical analysis of paraffin-embedded human liver tissue with Rabbit anti-Carboxylesterase 1/CES1 antibody (NBP3-32541) 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 (NBP3-32541) 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/nbp3-32541_rabbit-carboxylesterase-1-ces1-mab-je33-04-298202414304183.jpg)
![Immunocytochemistry/ Immunofluorescence: Carboxylesterase 1/CES1 Antibody (JE33-04) [NBP3-32541] - Immunocytochemistry analysis of U-937 cells labeling Carboxylesterase 1/CES1 with Rabbit anti-Carboxylesterase 1/CES1 antibody (NBP3-32541) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-Carboxylesterase 1/CES1 antibody (NBP3-32541) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI. Beta tubulin (red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594) was used as the secondary antibody at 1/1,000 dilution.](http://images.novusbio.com/fullsize/nbp3-32541_rabbit-carboxylesterase-1-ces1-mab-je33-04-2920241192346.jpg)
![Flow Cytometry: Carboxylesterase 1/CES1 Antibody (JE33-04) [NBP3-32541] - Flow cytometric analysis of U-937 cells labeling Carboxylesterase 1/CES1. Cells were fixed and permeabilized. Then stained with the primary antibody (NBP3-32541, 1ug/ml) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).](http://images.novusbio.com/fullsize/nbp3-32541_rabbit-carboxylesterase-1-ces1-mab-je33-04-39202488460.jpg)
![Western Blot: Clusterin/APOJ Antibody (Hs-3) [NB500-552] - Analysis of clusterin in human seminal plasma using anti-clusterin (Hs-3) purified.](http://images.novusbio.com/fullsize/Clusterin-APOJ-Antibody-Hs-3-Western-Blot-NB500-552-img0001.jpg "Western Blot: Clusterin/APOJ Antibody (Hs-3) [NB500-552] - Analysis of clusterin in human seminal plasma using anti-clusterin (Hs-3) purified.")
![Flow (Cell Surface): Neprilysin/CD10 Antibody (MEM-78) [NB500-372] - Surface staining of human peripheral blood with anti-human CD10 (MEM-78) PerCP-CyTM5.5.](http://images.novusbio.com/fullsize/Neprilysin-CD10-Antibody-MEM-78-Flow-Cell-Surface-NB500-372-img0006.jpg "Flow (Cell Surface): Neprilysin/CD10 Antibody (MEM-78) [NB500-372] - Surface staining of human peripheral blood with anti-human CD10 (MEM-78) PerCP-CyTM5.5.")
![Flow Cytometry: CD10 Antibody (MEM-78) [NB500-372]-Fig. 1. Surface staining of NALM-6 human pre-B cell leukemia cell line with anti-human CD10 (MEM-78) PE. Total viable cells were used for analysis.](http://images.novusbio.com/fullsize/p_444_1.jpg)
![Flow (Cell Surface): Neprilysin/CD10 Antibody (MEM-78) [NB500-372] - Surface staining of human peripheral blood with anti-human CD10 (MEM-78) APC.](http://images.novusbio.com/fullsize/Neprilysin-CD10-Antibody-MEM-78-Flow-Cell-Surface-NB500-372-img0001.jpg)
![Flow (Cell Surface): Neprilysin/CD10 Antibody (MEM-78) [NB500-372] - Surface staining of human peripheral blood with anti-human CD10 (MEM-78) APC-CyTM7.](http://images.novusbio.com/fullsize/Neprilysin-CD10-Antibody-MEM-78-Flow-Cell-Surface-NB500-372-img0002.jpg)
![Flow (Cell Surface): Neprilysin/CD10 Antibody (MEM-78) [NB500-372] - Surface staining of human peripheral blood with anti-human CD10 (MEM-78) PE-CyTM5.](http://images.novusbio.com/fullsize/Neprilysin-CD10-Antibody-MEM-78-Flow-Cell-Surface-NB500-372-img0003.jpg)
![Flow (Cell Surface): Neprilysin/CD10 Antibody (MEM-78) [NB500-372] - Surface staining of human peripheral blood with anti-human CD10 (MEM-78) PE-DyLigt(R) 594.](http://images.novusbio.com/fullsize/Neprilysin-CD10-Antibody-MEM-78-Flow-Cell-Surface-NB500-372-img0004.jpg)
![Flow (Cell Surface): Neprilysin/CD10 Antibody (MEM-78) [NB500-372] - Surface staining of human peripheral blood with anti-human CD10 (MEM-78) PerCP.](http://images.novusbio.com/fullsize/Neprilysin-CD10-Antibody-MEM-78-Flow-Cell-Surface-NB500-372-img0005.jpg)
![Western Blot: Tryptase alpha/TPS1 Antibody (SC68-07) [NBP2-67608] - Human skin tissue lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody ( 1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:5,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/Tryptase-alpha-TPS1-Antibody-SC68-07-Western-Blot-NBP2-67608-img0001.jpg "Western Blot: Tryptase alpha/TPS1 Antibody (SC68-07) [NBP2-67608] - Human skin tissue lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody ( 1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:5,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry-Paraffin: Tryptase alpha/TPS1 Antibody (SC68-07) [NBP2-67608] - Human lung tissue using anti-Mast Cell Tryptase antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (1/50) for 30 minutes 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/Tryptase-alpha-TPS1-Antibody-SC68-07-Immunohistochemistry-Paraffin-NBP2-67608-img0005.jpg)
![Immunohistochemistry-Paraffin: Tryptase alpha/TPS1 Antibody (SC68-07) [NBP2-67608] - Human tonsil tissue using anti-Mast Cell Tryptase antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (1/200) for 30 minutes 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/Tryptase-alpha-TPS1-Antibody-SC68-07-Immunohistochemistry-Paraffin-NBP2-67608-img0002.jpg)
![Immunohistochemistry-Paraffin: Tryptase alpha/TPS1 Antibody (SC68-07) [NBP2-67608] - Human small intestine tissue using anti-Mast Cell Tryptase antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (1/200) for 30 minutes 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/Tryptase-alpha-TPS1-Antibody-SC68-07-Immunohistochemistry-Paraffin-NBP2-67608-img0003.jpg)
![Immunohistochemistry-Paraffin: Tryptase alpha/TPS1 Antibody (SC68-07) [NBP2-67608] - Human prostate carcinoma tissue using anti-Mast Cell Tryptase antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (1/50) for 30 minutes 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/Tryptase-alpha-TPS1-Antibody-SC68-07-Immunohistochemistry-Paraffin-NBP2-67608-img0004.jpg)
![Western Blot: CD38 Antibody (PD01-49) [NBP3-32151] - Western blot analysis of CD38 on Daudi cell lysates with Rabbit anti-CD38 antibody (NBP3-32151) at 1/1,000 dilution. Lysates/proteins at 10 ug/Lane. Predicted band size: 34 kDa Observed band size: 45 kDa Exposure time: 2 minutes; 12% 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 (NBP3-32151) 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 1:300,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32151_rabbit-cd38-mab-pd01-49-278202416285274.jpg "Western Blot: CD38 Antibody (PD01-49) [NBP3-32151] - Western blot analysis of CD38 on Daudi cell lysates with Rabbit anti-CD38 antibody (NBP3-32151) at 1/1,000 dilution. Lysates/proteins at 10 ug/Lane. Predicted band size: 34 kDa Observed band size: 45 kDa Exposure time: 2 minutes; 12% 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 (NBP3-32151) 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 1:300,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: CD38 Antibody (PD01-49) [NBP3-32151] - Immunohistochemical analysis of paraffin-embedded human tonsil tissue with Rabbit anti-CD38 antibody (NBP3-32151) 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 (NBP3-32151) 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/nbp3-32151_rabbit-cd38-mab-pd01-49-29820241435231.jpg)
![Immunocytochemistry/ Immunofluorescence: CD38 Antibody (PD01-49) [NBP3-32151] - Immunocytochemistry analysis of A549 cells labeling CD38 with Rabbit anti-CD38 antibody (NBP3-32151) at 1/50 dilution. Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.05% Triton X-100 in PBS for 20 minutes, and then blocked with 2% negative goat serum for 30 minutes at room temperature. Cells were then incubated with Rabbit anti-CD38 antibody (NBP3-32151) at 1/50 dilution in 2% negative goat serum overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.](http://images.novusbio.com/fullsize/nbp3-32151_rabbit-cd38-mab-pd01-49-2920241192330.jpg)
![Flow Cytometry: CD38 Antibody (PD01-49) [NBP3-32151] - Flow cytometric analysis of THP-1 cells labeling CD38. Cells were washed twice with cold PBS and resuspend. Then stained with the primary antibody (NBP3-32151, 1μg/mL) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).](http://images.novusbio.com/fullsize/nbp3-32151_rabbit-cd38-mab-pd01-49-29202416453252.jpg)
![Western Blot: Chymase/CMA1/Mast Cell Chymase Antibody (JB74-32) [NBP2-75441] - Analysis of Chymase/CMA1/Mast Cell on different lysates with Rabbit anti-Chymase/CMA1/Mast Cell antibody at 1/500 dilution. Lane 1: Mouse spleen tissue lysate Lane 2: Rat spleen tissue lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 27 kDa Observed band size: 27 kDa Exposure time: 2 minutes; 15% 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 at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:300,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/Chymase-CMA1-Mast-Cell-Chymase-Antibody-JB74-32-Western-Blot-NBP2-75441-img0006.jpg "Western Blot: Chymase/CMA1/Mast Cell Chymase Antibody (JB74-32) [NBP2-75441] - Analysis of Chymase/CMA1/Mast Cell on different lysates with Rabbit anti-Chymase/CMA1/Mast Cell antibody at 1/500 dilution. Lane 1: Mouse spleen tissue lysate Lane 2: Rat spleen tissue lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 27 kDa Observed band size: 27 kDa Exposure time: 2 minutes; 15% 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 at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:300,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry-Paraffin: Chymase/CMA1/Mast Cell Chymase Antibody (JB74-32) [NBP2-75441] - Analysis of paraffin-embedded human lymph nodes tissue with Rabbit anti-Chymase/CMA1/Mast Cell Chymase antibody washed with ddH2O and PBS, and then probed with the primary antibody at 1/800 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/Chymase-CMA1-Mast-Cell-Chymase-Antibody-JB74-32-Immunohistochemistry-Paraffin-NBP2-75441-img0008.jpg)
![Immunohistochemistry-Paraffin: Chymase/CMA1/Mast Cell Chymase Antibody (JB74-32) [NBP2-75441] - Analysis of paraffin-embedded human tonsil tissue using anti-Mast Cell Chymase antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (1/50) for 30 minutes 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/Chymase-CMA1-Mast-Cell-Chymase-Antibody-JB74-32-Immunohistochemistry-Paraffin-NBP2-75441-img0004.jpg)
![Immunohistochemistry-Paraffin: Chymase/CMA1/Mast Cell Chymase Antibody (JB74-32) [NBP2-75441] - Human small intestine tissue using anti-Mast Cell Chymase antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (1/200) for 30 minutes 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/Chymase-CMA1-Mast-Cell-Chymase-Antibody-JB74-32-Immunohistochemistry-Paraffin-NBP2-75441-img0005.jpg)
![Immunohistochemistry-Paraffin: Chymase/CMA1/Mast Cell Chymase Antibody (JB74-32) [NBP2-75441] - Analysis of paraffin-embedded human skin tissue using anti-Mast Cell Chymase antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (1/50) for 30 minutes 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/Chymase-CMA1-Mast-Cell-Chymase-Antibody-JB74-32-Immunohistochemistry-Paraffin-NBP2-75441-img0003.jpg)
![Immunohistochemistry-Paraffin: Chymase/CMA1/Mast Cell Chymase Antibody (JB74-32) [NBP2-75441] - Analysis of paraffin-embedded human small intestine tissue with Rabbit anti-Chymase/CMA1/Mast Cell Chymase antibody washed with ddH2O and PBS, and then probed with the primary antibody at 1/800 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/Chymase-CMA1-Mast-Cell-Chymase-Antibody-JB74-32-Immunohistochemistry-Paraffin-NBP2-75441-img0007.jpg)
![Western Blot: TRAF-6 Antibody [NB100-56436] - Analysis of TRAF-6 using NB100-56436 in A) human thymus cell lysate and B) human testis cell lysate.](http://images.novusbio.com/fullsize/TRAF-6-Antibody-Western-Blot-NB100-56436-img0004.jpg "Western Blot: TRAF-6 Antibody [NB100-56436] - Analysis of TRAF-6 using NB100-56436 in A) human thymus cell lysate and B) human testis cell lysate.")
![Western Blot: CD74 Antibody (CLIP/813) [NBP2-44990] - Western Blot Analysis of Raji cell lysate using CD74 antibody (CLIP/813)](http://images.novusbio.com/fullsize/CD74-Antibody-CLIP-813-Western-Blot-NBP2-44990-img0005.jpg "Western Blot: CD74 Antibody (CLIP/813) [NBP2-44990] - Western Blot Analysis of Raji cell lysate using CD74 antibody (CLIP/813)")
![Immunocytochemistry/Immunofluorescence: CD74 Antibody (CLIP/813) [NBP2-44990] - Immunofluorescent staining of Raji cells. CD74 Antibody (CLIP/813) followed by goat anti-Mouse IgG-CF488 (Green). The nuclear counterstain is Red Dot (Red)](http://images.novusbio.com/fullsize/CD74-Antibody-CLIP-813-Immunocytochemistry-Immunofluorescence-NBP2-44990-img0002.jpg)
![Immunohistochemistry-Paraffin: CD74 Antibody (CLIP/813) [NBP2-44990] - Formalin-fixed, paraffin-embedded human Tonsil stained with CD74 Antibody (CLIP/813).](http://images.novusbio.com/fullsize/CD74-Antibody-CLIP-813-Immunohistochemistry-Paraffin-NBP2-44990-img0003.jpg)
![Flow Cytometry: CD74 Antibody (CLIP/813) [NBP2-44990] - Flow Cytometric Analysis of Human Raji cells. CD74 Antibody (CLIP/813) followed by goat anti-Mouse IgG-CF488 (Blue). Isotype Control (Red).](http://images.novusbio.com/fullsize/CD74-Antibody-CLIP-813-Flow-Cytometry-NBP2-44990-img0004.jpg)
![Western Blot: CD43/Sialophorin Antibody (DF-T1) [NBP2-15190] - Western Blot Analysis of K562 cell lysate using CD43/Sialophorin Antibody (DF-T1).](http://images.novusbio.com/fullsize/CD43-Sialophorin-Antibody-DF-T1-Western-Blot-NBP2-15190-img0010.jpg "Western Blot: CD43/Sialophorin Antibody (DF-T1) [NBP2-15190] - Western Blot Analysis of K562 cell lysate using CD43/Sialophorin Antibody (DF-T1).")
![Immunocytochemistry/Immunofluorescence: CD43/Sialophorin Antibody (DF-T1) [NBP2-15190] - Immunofluorescence Analysis of K562 cells labeling CD43 with CD43/Sialophorin Antibody (DF-T1) followed by Goat anti-Mouse IgG-CF488 (Green). The nuclear counterstain is NucSpot® Live 650](http://images.novusbio.com/fullsize/CD43-Sialophorin-Antibody-DF-T1-Immunocytochemistry-Immunofluorescence-NBP2-15190-img0009.jpg)
![Immunohistochemistry-Paraffin: CD43/Sialophorin Antibody (DF-T1) [NBP2-15190] - Formalin-paraffin human spleen stained with CD43 Ab (DF-T1).](http://images.novusbio.com/fullsize/CD43-Sialophorin-Antibody-DF-T1-Immunohistochemistry-Paraffin-NBP2-15190-img0007.jpg)
![Flow Cytometry: CD43/Sialophorin Antibody (DF-T1) [NBP2-15190] - Flow Cytometric Analysis of PFA-fixed K562 cells using CD43/Sialophorin Antibody (DF-T1) followed by Goat anti-Mouse IgG-CF488 (Blue); Isotype Control (Red).](http://images.novusbio.com/fullsize/CD43-Sialophorin-Antibody-DF-T1-Flow-Cytometry-NBP2-15190-img0008.jpg)
![Western Blot: CD43/Sialophorin Antibody (SPN/1766R) [NBP2-53288] - Western Blot Analysis of K562 cell lysate using CD43/Sialophorin Antibody (SPN/1766R).](http://images.novusbio.com/fullsize/CD43-Sialophorin-Antibody-SPN-1766R-Western-Blot-NBP2-53288-img0004.jpg "Western Blot: CD43/Sialophorin Antibody (SPN/1766R) [NBP2-53288] - Western Blot Analysis of K562 cell lysate using CD43/Sialophorin Antibody (SPN/1766R).")
![Immunocytochemistry/Immunofluorescence: CD43/Sialophorin Antibody (SPN/1766R) [NBP2-53288] - Immunofluorescence Analysis of K562 cells labeling CD43 with CD43/Sialophorin Antibody (SPN/1766R) followed by Goat anti-Rabbit- IgG-CF488 (Green). The nuclear counterstain is NucSpot .](http://images.novusbio.com/fullsize/CD43-Sialophorin-Antibody-SPN-1766R-Immunocytochemistry-Immunofluorescence-NBP2-53288-img0003.jpg)
![Immunohistochemistry-Paraffin: CD43/Sialophorin Antibody (SPN/1766R) [NBP2-53288] - Formalin-fixed, paraffin-embedded human Tonsil stained with CD43 Recombinant Rabbit Monoclonal Antibody (SPN/1766R).](http://images.novusbio.com/fullsize/CD43-Sialophorin-Antibody-SPN-1766R-Immunohistochemistry-Paraffin-NBP2-53288-img0001.jpg)
![Flow Cytometry: CD43/Sialophorin Antibody (SPN/1766R) [NBP2-53288] - Flow Cytometric Analysis of PFA-fixed K562 cells using CD43/Sialophorin Antibody (SPN/1766R) followed by Goat anti-Rabbit- IgG-CF488 (Blue); Isotype Control (Red)](http://images.novusbio.com/fullsize/CD43-Sialophorin-Antibody-SPN-1766R-Flow-Cytometry-NBP2-53288-img0002.jpg)
![Western Blot: c-Maf Antibody [NB600-267] - Nuclear extract (6 ug) from HeLa cells transfected with empty vector or expression constructs for mouse MafA, mouse MafB or mouse cMaf. Antibody used at 0.4 ug/ml.](http://images.novusbio.com/fullsize/c-Maf-Antibody-Western-Blot-NB600-267-img0005.jpg "Western Blot: c-Maf Antibody [NB600-267] - Nuclear extract (6 ug) from HeLa cells transfected with empty vector or expression constructs for mouse MafA, mouse MafB or mouse cMaf. Antibody used at 0.4 ug/ml.")