| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| IHC-Prediluted | NBP2-45107 | |||
| Azide and BSA Free | NBP2-34612-0.1mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-33150 | |||
| IHC-Prediluted | NBP2-44388 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-47909-0.1mg | |||
| IHC-Prediluted | NBP2-48362 | |||
| Conjugate | Catalog # | Availability | Size | Price |
|---|---|---|---|---|
| Allophycocyanin | NB758APC | |||
| Biotin | NB758B | |||
| DyLight 350 | NB758UV | |||
| DyLight 405 | NB758V | |||
| DyLight 488 | NB758G | |||
| DyLight 550 | NB758R | |||
| DyLight 594 | NB758DL594 | |||
| DyLight 650 | NB758C | |||
| DyLight 680 | NB758FR | |||
| DyLight 755 | NB758IR | |||
| FITC | NB760 | |||
| HRP | NB761 | |||
| Janelia Fluor 525 | NB758JF525 | |||
| Janelia Fluor 669 | NB758JF669 | |||
| PE | NB758PE | |||
| PerCP | NB758PCP | |||
![Flow Cytometry: CD8 Antibody (OX-8) [NBP2-12523] - Separation of rat CD8a positive thymocytes (red-filled) from CD8a negative thymocytes (black-dashed) in flow cytometry analysis (surface staining) of rat thymocyte suspension stained using anti-rat CD8 (OX-8) purified antibody (concentration in sample 0.32 ug/ml) GAM APC.](http://images.novusbio.com/fullsize/CD8-Antibody-OX-8-Flow-Cytometry-NBP2-12523-img0002.jpg "Flow Cytometry: CD8 Antibody (OX-8) [NBP2-12523] - Separation of rat CD8a positive thymocytes (red-filled) from CD8a negative thymocytes (black-dashed) in flow cytometry analysis (surface staining) of rat thymocyte suspension stained using anti-rat CD8 (OX-8) purified antibody (concentration in sample 0.32 ug/ml) GAM APC.")
![Flow Cytometry: CD8 Antibody (OX-8) [NBP2-12523] - Flow cytometry surface staining pattern of rat thymocyte suspension stained using anti-rat CD8 (OX-8) purified antibody (concentration in sample 0.32 ug/ml) GAM APC.](http://images.novusbio.com/fullsize/CD8-Antibody-OX-8-Flow-Cytometry-NBP2-12523-img0001.jpg)
![Flow (Cell Surface): ICAM-1/CD54 Antibody (1H4) - Azide Free [NB110-58732] - Surface staining of human peripheral blood with anti-CD54 (1H4) FITC. Image using the FITC format of this antibody.](http://images.novusbio.com/fullsize/ICAM-1-CD54-Antibody-1H4-Azide-Free-Flow-Cell-Surface-NB110-58732-img0010.jpg "Flow (Cell Surface): ICAM-1/CD54 Antibody (1H4) - Azide Free [NB110-58732] - Surface staining of human peripheral blood with anti-CD54 (1H4) FITC. Image using the FITC format of this antibody.")
![Flow Cytometry: ICAM-1/CD54 Antibody (1H4) - Azide Free [NB110-58732] - Expression of CD54 in normal human peripheral blood, as detected with anti-CD54 (1H4) biotin.](http://images.novusbio.com/fullsize/ICAM-1-CD54-Antibody-1H4-Azide-Free-Flow-Cytometry-NB110-58732-img0004.jpg)
![Flow Cytometry: ICAM-1/CD54 Antibody (1H4) - Azide Free [NB110-58732] - Fig. 1. Surface staining of U937 human histiocytic lymphoma cell line with anti-human CD54 (1H4) PE. Total viable cells were used for analysis. Image using the Biotin form of this antibody.](http://images.novusbio.com/fullsize/ICAM-1-CD54-Antibody-1H4-Azide-Free-Flow-Cytometry-NB110-58732-img0005.jpg)
![Flow Cytometry: ICAM-1/CD54 Antibody (1H4) - Azide Free [NB110-58732] - Staining of human peripheral blood with anti-CD54 (1H4) APC.](http://images.novusbio.com/fullsize/ICAM-1-CD54-Antibody-1H4-Azide-Free-Flow-Cytometry-NB110-58732-img0007.jpg)
![Flow Cytometry: ICAM-1/CD54 Antibody (1H4) - Azide Free [NB110-58732] - Staining of human peripheral blood with anti-CD54 (1H4) Alexa Fluor (R) 700.](http://images.novusbio.com/fullsize/ICAM-1-CD54-Antibody-1H4-Azide-Free-Flow-Cytometry-NB110-58732-img0009.jpg)
![Flow Cytometry: ICAM-1/CD54 Antibody (1H4) - Azide Free [NB110-58732] - Surface staining of human peripheral blood with anti-CD54 (1H4) PerCP. Image from the PE version of this antibody.](http://images.novusbio.com/fullsize/ICAM-1-CD54-Antibody-1H4-Azide-Free-Flow-Cytometry-NB110-58732-img0006.jpg)
![Western Blot: CD43/Sialophorin Antibody (MEM-59) - Low Endotoxin [NBP2-62227] - Analysis (non-reducing conditions) of isolated peripheral blood lymphocytes of various species using anti-human CD43 (MEM-59).Lane 1: lysate of human PBLLane 2: lysate of canine PBLLane 3: lysate of porcine PBL](http://images.novusbio.com/fullsize/CD43-Sialophorin-Antibody-MEM-59-Low-Endotoxin-Western-Blot-NBP2-62227-img0005.jpg "Western Blot: CD43/Sialophorin Antibody (MEM-59) - Low Endotoxin [NBP2-62227] - Analysis (non-reducing conditions) of isolated peripheral blood lymphocytes of various species using anti-human CD43 (MEM-59).Lane 1: lysate of human PBLLane 2: lysate of canine PBLLane 3: lysate of porcine PBL")
![Immunohistochemistry-Paraffin: CD43/Sialophorin Antibody (MEM-59) - Low Endotoxin [NBP2-62227] - Staining of human spleen (paraffin sections) using anti-CD43 (MEM-59).](http://images.novusbio.com/fullsize/CD43-Sialophorin-Antibody-MEM-59-Low-Endotoxin-Immunohistochemistry-Paraffin-NBP2-62227-img0006.jpg)
![Flow (Cell Surface): CD43/Sialophorin Antibody (MEM-59) - Low Endotoxin [NBP2-62227] - Surface staining of human peripheral blood with anti-CD43 (MEM-59) PE.](http://images.novusbio.com/fullsize/CD43-Sialophorin-Antibody-MEM-59-Low-Endotoxin-Flow-Cell-Surface-NBP2-62227-img0004.jpg)
![Flow (Cell Surface): CD43/Sialophorin Antibody (MEM-59) - Low Endotoxin [NBP2-62227] - Surface staining of human peripheral blood with anti-CD43 (MEM-59) APC-CyTM7.](http://images.novusbio.com/fullsize/CD43-Sialophorin-Antibody-MEM-59-Low-Endotoxin-Flow-Cell-Surface-NBP2-62227-img0001.jpg)
![Flow (Cell Surface): CD43/Sialophorin Antibody (MEM-59) - Low Endotoxin [NBP2-62227] - Surface staining of human peripheral blood with anti-CD43 (MEM-59) biotin / streptavidin-APC.](http://images.novusbio.com/fullsize/CD43-Sialophorin-Antibody-MEM-59-Low-Endotoxin-Flow-Cell-Surface-NBP2-62227-img0002.jpg)
![Flow (Cell Surface): CD43/Sialophorin Antibody (MEM-59) - Low Endotoxin [NBP2-62227] - Surface staining of human peripheral blood with anti-CD43 (MEM-59) FITC.](http://images.novusbio.com/fullsize/CD43-Sialophorin-Antibody-MEM-59-Low-Endotoxin-Flow-Cell-Surface-NBP2-62227-img0003.jpg)
![Western Blot: LAMP-2/CD107b Antibody (C9-9) [NBP2-66929] - Western blot analysis of LAMP-2/CD107b on Hela cell lysate. 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-Mouse IgG - HRP Secondary Antibody (HA1006) at 1:5,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/LAMP-2-CD107b-Antibody-C9-9-Western-Blot-NBP2-66929-img0006.jpg "Western Blot: LAMP-2/CD107b Antibody (C9-9) [NBP2-66929] - Western blot analysis of LAMP-2/CD107b on Hela cell lysate. 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-Mouse IgG - HRP Secondary Antibody (HA1006) at 1:5,000 dilution was used for 1 hour at room temperature.")
![Immunocytochemistry/Immunofluorescence: LAMP-2/CD107b Antibody (C9-9) [NBP2-66929] - ICC staining of LAMP2 in HepG2 cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the primary antibody (1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 Goat anti-mouse IgG was used as the secondary antibody at 1/100 dilution. The nuclear counter stain is DAPI (blue).](http://images.novusbio.com/fullsize/LAMP-2-CD107b-Antibody-C9-9-Immunocytochemistry-Immunofluorescence-NBP2-66929-img0007.jpg)
![Immunohistochemistry-Paraffin: LAMP-2/CD107b Antibody (C9-9) [NBP2-66929] - Immunohistochemical analysis of paraffin-embedded human pancreas tissue using anti-LAMP-2/CD107b 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/LAMP-2-CD107b-Antibody-C9-9-Immunohistochemistry-Paraffin-NBP2-66929-img0005.jpg)
![Flow Cytometry: LAMP-2/CD107b Antibody (C9-9) [NBP2-66929] - Flow cytometric analysis of LAMP-2/CD107b was done on Hela cells. The cells were fixed, permeabilized and stained with the primary antibody (1/100) (red). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor 488-conjugated goat anti-mouse IgG Secondary antibody at 1/500 dilution for 30 minutes. Unlabeled sample was used as a control (cells without incubation with primary antibody; black).](http://images.novusbio.com/fullsize/LAMP-2-CD107b-Antibody-C9-9-Flow-Cytometry-NBP2-66929-img0001.jpg)
![Immunocytochemistry/Immunofluorescence: LAMP-2/CD107b Antibody (C9-9) [NBP2-66929] - ICC staining of LAMP-2/CD107b in Hela cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the primary antibody (1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor(R)488 Goat anti-mouse IgG was used as the secondary antibody at 1/100 dilution. The nuclear counter stain is DAPI (blue).](http://images.novusbio.com/fullsize/LAMP-2-CD107b-Antibody-C9-9-Immunocytochemistry-Immunofluorescence-NBP2-66929-img0002.jpg)
![Immunohistochemistry-Paraffin: LAMP-2/CD107b Antibody (C9-9) [NBP2-66929] - Immunohistochemical analysis of paraffin-embedded human kidney tissue using anti-LAMP-2/CD107b 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/LAMP-2-CD107b-Antibody-C9-9-Immunohistochemistry-Paraffin-NBP2-66929-img0003.jpg)
![Immunohistochemistry-Paraffin: LAMP-2/CD107b Antibody (C9-9) [NBP2-66929] - Immunohistochemical analysis of paraffin-embedded human liver tissue using anti-LAMP-2/CD107b 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/LAMP-2-CD107b-Antibody-C9-9-Immunohistochemistry-Paraffin-NBP2-66929-img0004.jpg)
![Western Blot: Rabbit Monoclonal FAT10 Antibody (JJ084-09) [NBP2-67917] - Western blot analysis of Ubiquitin D on different lysates with Rabbit anti-Ubiquitin D antibody (NBP2-67917) at 1/2,000 dilution.Lane 1: HeLa cell lysateLane 2: HepG2 cell lysateLane 3: NIH/3T3 cell lysateLysates/proteins at 20 µg/Lane.Predicted band size: 18 kDaObserved band size: 20 kDaExposure time: 26 seconds; ECL: K1801;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 (NBP2-67917) at 1/2,000 dilution was used in 5% NFDM/TBST at 4℃ 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/nbp2-67917_rabbit-monoclonal-fat10-antibody-jj084-09-western-blot-1312026165644.jpg "Western Blot: Rabbit Monoclonal FAT10 Antibody (JJ084-09) [NBP2-67917] - Western blot analysis of Ubiquitin D on different lysates with Rabbit anti-Ubiquitin D antibody (NBP2-67917) at 1/2,000 dilution.Lane 1: HeLa cell lysateLane 2: HepG2 cell lysateLane 3: NIH/3T3 cell lysateLysates/proteins at 20 µg/Lane.Predicted band size: 18 kDaObserved band size: 20 kDaExposure time: 26 seconds; ECL: K1801;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 (NBP2-67917) at 1/2,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.")
![Immunocytochemistry/Immunofluorescence: FAT10 Antibody (JJ084-09) [NBP2-67917] - ICC staining of Ubiquitin D in Hela cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the primary antibody (NBP2-67917, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue).](http://images.novusbio.com/fullsize/FAT10-Antibody-JJ084-09-Immunocytochemistry-Immunofluorescence-NBP2-67917-img0001.jpg)
![Immunocytochemistry/Immunofluorescence: FAT10 Antibody (JJ084-09) [NBP2-67917] - ICC staining of Ubiquitin D in F9 cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the primary antibody (NBP2-67917, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue).](http://images.novusbio.com/fullsize/FAT10-Antibody-JJ084-09-Immunocytochemistry-Immunofluorescence-NBP2-67917-img0006.jpg)
![Immunocytochemistry/Immunofluorescence: FAT10 Antibody (JJ084-09) [NBP2-67917] - ICC staining of Ubiquitin D in HepG2 cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the primary antibody (NBP2-67917, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue).](http://images.novusbio.com/fullsize/FAT10-Antibody-JJ084-09-Immunocytochemistry-Immunofluorescence-NBP2-67917-img0002.jpg)
![Immunohistochemistry: Rabbit Monoclonal FAT10 Antibody (JJ084-09) [NBP2-67917] - Immunohistochemical analysis of paraffin-embedded human kidney tissue with Rabbit anti-Ubiquitin D antibody (NBP2-67917) at 1/200 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 (NBP2-67917) at 1/200 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/nbp2-67917_rabbit-monoclonal-fat10-antibody-jj084-09-immunohistochemistry-paraffin-131202617029.jpg)
![Immunohistochemistry: Rabbit Monoclonal FAT10 Antibody (JJ084-09) [NBP2-67917] - Immunohistochemical analysis of paraffin-embedded mouse kidney tissue with Rabbit anti-Ubiquitin D antibody (NBP2-67917) 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 (NBP2-67917) 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/nbp2-67917_rabbit-monoclonal-fat10-antibody-jj084-09-immunohistochemistry-paraffin-131202617226.jpg)
![Immunohistochemistry: Rabbit Monoclonal FAT10 Antibody (JJ084-09) [NBP2-67917] - Immunohistochemical analysis of paraffin-embedded rat kidney tissue with Rabbit anti-Ubiquitin D antibody (NBP2-67917) at 1/200 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 (NBP2-67917) at 1/200 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/nbp2-67917_rabbit-monoclonal-fat10-antibody-jj084-09-immunohistochemistry-paraffin-131202617524.jpg)
![Western Blot: CD40 Ligand/TNFSF5 Antibody (JM11-34) [NBP2-66756] - Western blot analysis of CD40 Ligand/TNFSF5 on different 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 (HA1001) at 1:5,000 dilution was used for 1 hour at room temperature. Positive control: Lane 1: mouse liver tissue lysate Lane 2: rat liver tissue lysate Lane 2: mouse bone marrow tissue lysate](http://images.novusbio.com/fullsize/CD40-Ligand-TNFSF5-Antibody-JM11-34-Western-Blot-NBP2-66756-img0007.jpg "Western Blot: CD40 Ligand/TNFSF5 Antibody (JM11-34) [NBP2-66756] - Western blot analysis of CD40 Ligand/TNFSF5 on different 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 (HA1001) at 1:5,000 dilution was used for 1 hour at room temperature. Positive control: Lane 1: mouse liver tissue lysate Lane 2: rat liver tissue lysate Lane 2: mouse bone marrow tissue lysate")
![Immunocytochemistry/Immunofluorescence: CD40 Ligand/TNFSF5 Antibody (JM11-34) [NBP2-66756] - Staining CD40L in NIH-3T3 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](http://images.novusbio.com/fullsize/CD40-Ligand-TNFSF5-Antibody-JM11-34-Immunocytochemistry-Immunofluorescence-NBP2-66756-img0006.jpg)
![Immunohistochemistry-Paraffin: CD40 Ligand/TNFSF5 Antibody (JM11-34) [NBP2-66756] - Analysis of paraffin-embedded human spleen tissue using anti- CD40L antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/CD40-Ligand-TNFSF5-Antibody-JM11-34-Immunohistochemistry-Paraffin-NBP2-66756-img0004.jpg)
![Flow Cytometry: CD40 Ligand/TNFSF5 Antibody (JM11-34) [NBP2-66756] - Analysis of THP-1 cells with CD40L antibody at 1/50 dilution (red) compared with an unlabelled control (cells without incubation with primary antibody; black). Alexa Fluor 488-conjugated goat anti rabbit IgG was used as the secondary antibody.](http://images.novusbio.com/fullsize/CD40-Ligand-TNFSF5-Antibody-JM11-34-Flow-Cytometry-NBP2-66756-img0001.jpg)
![Immunocytochemistry/Immunofluorescence: CD40 Ligand/TNFSF5 Antibody (JM11-34) [NBP2-66756] - Staining CD40L in Hela cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](http://images.novusbio.com/fullsize/CD40-Ligand-TNFSF5-Antibody-JM11-34-Immunocytochemistry-Immunofluorescence-NBP2-66756-img0002.jpg)
![Immunocytochemistry/Immunofluorescence: CD40 Ligand/TNFSF5 Antibody (JM11-34) [NBP2-66756] - Staining CD40L in MCF-7 cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](http://images.novusbio.com/fullsize/CD40-Ligand-TNFSF5-Antibody-JM11-34-Immunocytochemistry-Immunofluorescence-NBP2-66756-img0003.jpg)
![Immunohistochemistry: CD52 Antibody (Campath-1H) [NBP2-75896] - Anti-CD52 staining of formaldehyde fixed paraffin embedded rat thymus tissue, at 40x magnification. The human IgG1-chimeric version of Campath-1H (NBP2-75896) was used to stain samples at a concentration of 5 ug/ml.](http://images.novusbio.com/fullsize/CD52-Antibody-Campath-1H-Immunohistochemistry-NBP2-75896-img0006.jpg "Immunohistochemistry: CD52 Antibody (Campath-1H) [NBP2-75896] - Anti-CD52 staining of formaldehyde fixed paraffin embedded rat thymus tissue, at 40x magnification. The human IgG1-chimeric version of Campath-1H (NBP2-75896) was used to stain samples at a concentration of 5 ug/ml.")
![Immunohistochemistry: CD52 Antibody (Campath-1H) [NBP2-75896] - Formalin fixed human thyroid cancer slices were were stained with a NBP2-75896 at 5 ug/ml.](http://images.novusbio.com/fullsize/CD52-Antibody-Campath-1H-Immunohistochemistry-NBP2-75896-img0003.jpg)
![Immunohistochemistry: CD52 Antibody (Campath-1H) [NBP2-75896] - Anti-CD52 staining of formaldehyde fixed paraffin embedded rat epididymis tissue, at 40x magnification. The human IgG1-chimeric version of Campath-1H (NBP2-75896) was used to stain samples at a concentration of 5 ug/ml.](http://images.novusbio.com/fullsize/CD52-Antibody-Campath-1H-Immunohistochemistry-NBP2-75896-img0004.jpg)
![Immunohistochemistry: CD52 Antibody (Campath-1H) [NBP2-75896] - Anti-CD52 staining of formaldehyde fixed paraffin embedded rat spleen tissue, at 40x magnification. The human IgG1-chimeric version of Campath-1H (NBP2-75896) was used to stain samples at a concentration of 5 ug/ml.](http://images.novusbio.com/fullsize/CD52-Antibody-Campath-1H-Immunohistochemistry-NBP2-75896-img0005.jpg)
![Immunofluorescence: CD52 Antibody (Campath-1H) [NBP2-75896] - Formaldehyde-fixed rat thymus slices were stained with NBP2-75896 at 5 ug/ml and detected with a FITC-conjugated secondary antibody.](http://images.novusbio.com/fullsize/CD52-Antibody-Campath-1H-Immunofluorescence-NBP2-75896-img0002.jpg)
![Immunohistochemistry-Paraffin: Insulin Antibody (E2-E3 + 2D11-H5 (same as INS04 + INS05)) [NBP2-34261] - Adult human pancreas. Antibody 1:200; heat-induced epitope retrieval with citrate buffer. Image from verified customer review.](http://images.novusbio.com/fullsize/Insulin-Antibody-E2-E3-+-2D11-H5-same-as-INS04-+-INS05-Immunohistochemistry-Paraffin-NBP2-34261-img0004.jpg "Immunohistochemistry-Paraffin: Insulin Antibody (E2-E3 + 2D11-H5 (same as INS04 + INS05)) [NBP2-34261] - Adult human pancreas. Antibody 1:200; heat-induced epitope retrieval with citrate buffer. Image from verified customer review.")
![Immunohistochemistry-Paraffin: Insulin Antibody (E2-E3 + 2D11-H5 (same as INS04 + INS05)) [NBP2-34261] - Formalin-fixed, paraffin-embedded human pancreas stained with insulin Monoclonal Antibody (E2-E3+2D11-H5).](http://images.novusbio.com/fullsize/Insulin-Antibody-E2-E3-+-2D11-H5-same-as-INS04-+-INS05-Immunohistochemistry-Paraffin-NBP2-34261-img0002.jpg)
![Western Blot: Melan-A/MART-1 Antibody (M2-9E3) [NBP2-15198] - Western Blot Analysis of COLO38 cell lysate using Melan-A/MART-1 Antibody (M2-9E3).](http://images.novusbio.com/fullsize/Melan-A-MART-1-Antibody-M2-9E3-Western-Blot-NBP2-15198-img0005.jpg "Western Blot: Melan-A/MART-1 Antibody (M2-9E3) [NBP2-15198] - Western Blot Analysis of COLO38 cell lysate using Melan-A/MART-1 Antibody (M2-9E3).")
![Immunohistochemistry-Paraffin: Melan-A/MART-1 Antibody (M2-9E3) [NBP2-15198] - Formalin-paraffin human melanoma stained with Melan-A Ab (M2-9E3). Note cytoplasmic staining of cells.](http://images.novusbio.com/fullsize/Melan-A-MART-1-Antibody-M2-9E3-Immunohistochemistry-Paraffin-NBP2-15198-img0004.jpg)
![Immunohistochemistry-Paraffin: Melan-A/MART-1 Antibody (M2-9E3) [NBP2-15198] - Formalin-paraffin human melanoma stained with Melan-A Ab (M2-9E3). Note cytoplasmic staining of cells.](http://images.novusbio.com/fullsize/Melan-A-MART-1-Antibody-M2-9E3-Immunohistochemistry-Paraffin-NBP2-15198-img0003.jpg)
![Immunohistochemistry: CD34 Antibody (QBEnd/10 + HPCA1/763) [NBP2-44567] - Representative images of RCC patient biopsies immunostained for VEGFR2, CD34, and NRP1 and counterstained using Hoechst33342. Left column shows examples of NRP1 expressed by endothelial cells; middle column shows a tumor sample with low NRP1 expression. Right column shows NRP1 positive perivascular tumor cells. Blood vessels were stained for CD34 and nuclei counterstained using Hoechst33342. Left column shows cis complexes, localized within the endothelium. Middle column shows a tumor lacking VEGFR2/NRP1 complexes. Right column shows trans complexes, located adjacent to the endothelium (white arrowheads). Image collected and cropped by Citeab from the following publication (Perivascular Neuropilin-1 expression is an independent marker of improved survival in renal cell carcinoma. J Pathol (2020) licensed under a CC-BY license.](http://images.novusbio.com/fullsize/CD34-Antibody-QBEnd-10-+-HPCA1-763-Immunohistochemistry-NBP2-44567-img0005.jpg "Immunohistochemistry: CD34 Antibody (QBEnd/10 + HPCA1/763) [NBP2-44567] - Representative images of RCC patient biopsies immunostained for VEGFR2, CD34, and NRP1 and counterstained using Hoechst33342. Left column shows examples of NRP1 expressed by endothelial cells; middle column shows a tumor sample with low NRP1 expression. Right column shows NRP1 positive perivascular tumor cells. Blood vessels were stained for CD34 and nuclei counterstained using Hoechst33342. Left column shows cis complexes, localized within the endothelium. Middle column shows a tumor lacking VEGFR2/NRP1 complexes. Right column shows trans complexes, located adjacent to the endothelium (white arrowheads). Image collected and cropped by Citeab from the following publication (Perivascular Neuropilin-1 expression is an independent marker of improved survival in renal cell carcinoma. J Pathol (2020) licensed under a CC-BY license.")
![Immunohistochemistry-Paraffin: CD34 Antibody (QBEnd/10 + HPCA1/763) [NBP2-44567] - Human Angiosarcoma stained with CD34 Monoclonal Antibody (QBEnd/10 + HPCA1/763)](http://images.novusbio.com/fullsize/CD34-Antibody-QBEnd-10-+-HPCA1-763-Immunohistochemistry-Paraffin-NBP2-44567-img0001.jpg)
![Immunohistochemistry-Paraffin: CD34 Antibody (QBEnd/10 + HPCA1/763) [NBP2-44567] - Human Colon Carcinoma stained with CD34 Monoclonal Antibody (QBEnd/10 + HPCA1/763)](http://images.novusbio.com/fullsize/CD34-Antibody-QBEnd-10-+-HPCA1-763-Immunohistochemistry-Paraffin-NBP2-44567-img0002.jpg)
![Immunohistochemistry-Paraffin: CD34 Antibody (QBEnd/10 + HPCA1/763) [NBP2-44567] - Human Placenta stained with CD34 Monoclonal Antibody (QBEnd/10 + HPCA1/763)](http://images.novusbio.com/fullsize/CD34-Antibody-QBEnd-10-+-HPCA1-763-Immunohistochemistry-Paraffin-NBP2-44567-img0003.jpg)
![Immunohistochemistry-Paraffin: CD34 Antibody (QBEnd/10 + HPCA1/763) [NBP2-44567] - Human Tonsil stained with CD34 Monoclonal Antibody (QBEnd/10 + HPCA1/763)](http://images.novusbio.com/fullsize/CD34-Antibody-QBEnd-10-+-HPCA1-763-Immunohistochemistry-Paraffin-NBP2-44567-img0004.jpg)