| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-44196 | |||
| BSA Free | NBP2-61428-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-89474-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-58697-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-52681-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-75910SS | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26682-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26300-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-52670-0.025mg | |||
![Immunocytochemistry/Immunofluorescence: Nanog Antibody (CL5803) [NBP2-61428] - Staining of NTERA-2 cells using the Anti-NANOG monoclonal antibody, showing specific staining in the nucleoplasm in green. Microtubule and nuclear probes are visualized in red and blue, respectively (where available). Antibody staining is shown in green.](http://images.novusbio.com/fullsize/Nanog-Antibody-CL5803-Immunocytochemistry-Immunofluorescence-NBP2-61428-img0001.jpg "Immunocytochemistry/Immunofluorescence: Nanog Antibody (CL5803) [NBP2-61428] - Staining of NTERA-2 cells using the Anti-NANOG monoclonal antibody, showing specific staining in the nucleoplasm in green. Microtubule and nuclear probes are visualized in red and blue, respectively (where available). Antibody staining is shown in green.")
![Immunohistochemistry-Paraffin: Nanog Antibody (CL5803) [NBP2-61428] - Staining of human testis shows absence of positivity as expected (negative control).](http://images.novusbio.com/fullsize/Nanog-Antibody-CL5803-Immunohistochemistry-Paraffin-NBP2-61428-img0004.jpg)
![Immunohistochemistry-Paraffin: Nanog Antibody (CL5803) [NBP2-61428] - Staining of human testis cancer shows strong nuclear immunoreactivity in tumor cells.](http://images.novusbio.com/fullsize/Nanog-Antibody-CL5803-Immunohistochemistry-Paraffin-NBP2-61428-img0002.jpg)
![Immunohistochemistry-Paraffin: Nanog Antibody (CL5803) [NBP2-61428] - Staining of human bladder cancer shows absence of positivity in tumor cells as expected (negative control).](http://images.novusbio.com/fullsize/Nanog-Antibody-CL5803-Immunohistochemistry-Paraffin-NBP2-61428-img0003.jpg)
![<b>Orthogonal Strategies Validation. </b>Immunohistochemistry-Paraffin: STAT4 Antibody [NBP1-89474] - Staining of human testis shows high expression.](http://images.novusbio.com/fullsize/STAT4-Antibody-Immunohistochemistry-Paraffin-NBP1-89474-img0007.jpg)
![Immunohistochemistry-Paraffin: STAT4 Antibody [NBP1-89474] - Staining of human skeletal muscle shows low expression as expected.](http://images.novusbio.com/fullsize/STAT4-Antibody-Immunohistochemistry-Paraffin-NBP1-89474-img0006.jpg)
![Flow Cytometry: CD4 Antibody (HAL36A) [NBP2-60895] - Test of cross-reactivity of antibodies between closely related species, the Syrian hamster and the bank vole. Family: Cricetidae. Bank vole thymocytes were stained with Mouse Anti-hamster CD4 Monoclonal Antibody 1:100 (NBP2-60895), followed by FITC-conjugated Anti-Mouse IgG Secondary Antibody. Cells were analyzed with CytoFLEX (Beckman Coulter). The clone (HAL36A) does cross-react with bank vole CD4. Bank vole thymocytes. Gating: lymphocytes. A: no staining. B: control staining, only secondary mAb. C: primary anti-Syrian hamster CD4 Antibody + secondary antibody. D: Gating, all events, overlay: black as in A, blue as in B, green as in C.](http://images.novusbio.com/fullsize/CD4-Antibody-HAL36A-Flow-Cytometry-NBP2-60895-img0002.jpg "Flow Cytometry: CD4 Antibody (HAL36A) [NBP2-60895] - Test of cross-reactivity of antibodies between closely related species, the Syrian hamster and the bank vole. Family: Cricetidae. Bank vole thymocytes were stained with Mouse Anti-hamster CD4 Monoclonal Antibody 1:100 (NBP2-60895), followed by FITC-conjugated Anti-Mouse IgG Secondary Antibody. Cells were analyzed with CytoFLEX (Beckman Coulter). The clone (HAL36A) does cross-react with bank vole CD4. Bank vole thymocytes. Gating: lymphocytes. A: no staining. B: control staining, only secondary mAb. C: primary anti-Syrian hamster CD4 Antibody + secondary antibody. D: Gating, all events, overlay: black as in A, blue as in B, green as in C.")
![Flow Cytometry: CD4 Antibody (HAL36A) [NBP2-60895] - Flow cytometry analysis of hamster leukocytes.](http://images.novusbio.com/fullsize/CD4-Antibody-HAL36A-Flow-Cytometry-NBP2-60895-img0001.jpg)
![Western Blot: STAT4 Antibody (10H10O9) [NBP3-16425] - Western blot analysis of extracts of various cell lines, using STAT4 Rabbit mAb (NBP3-16425) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 90s.](http://images.novusbio.com/fullsize/STAT4-Antibody-10H10O9-Western-Blot-NBP3-16425-img0003.jpg "Western Blot: STAT4 Antibody (10H10O9) [NBP3-16425] - Western blot analysis of extracts of various cell lines, using STAT4 Rabbit mAb (NBP3-16425) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 90s.")
![Immunocytochemistry/Immunofluorescence: STAT4 Antibody (10H10O9) [NBP3-16425] - Immunofluorescence analysis of C6 cells using STAT4 Rabbit mAb (NBP3-16425) at dilution of 1:100 (40x lens). Blue: DAPI for nuclear staining.](http://images.novusbio.com/fullsize/STAT4-Antibody-10H10O9-Immunocytochemistry-Immunofluorescence-NBP3-16425-img0001.jpg)
![Immunocytochemistry/ Immunofluorescence: STAT4 Antibody (10H10O9) [NBP3-16425] - Immunofluorescence analysis of NIH-3T3 cells using STAT4 Rabbit mAb at dilution of 1:100 (40x lens). Secondary antibody: Cy3 Goat Anti-Rabbit IgG (H+L) at 1:500 dilution. Blue: DAPI for nuclear staining.](http://images.novusbio.com/fullsize/nbp3-16425_rabbit-stat4-mab-10h10o9-7220251245312.jpg)
![Western Blot: FoxP3 Antibody [NBP2-58697] - Western blot analysis in human cell line RT-4, human cell line U-251 MG, human plasma, human liver tissue and human tonsil tissue.](http://images.novusbio.com/fullsize/FoxP3-Antibody-Western-Blot-NBP2-58697-img0002.jpg "Western Blot: FoxP3 Antibody [NBP2-58697] - Western blot analysis in human cell line RT-4, human cell line U-251 MG, human plasma, human liver tissue and human tonsil tissue.")
![Immunocytochemistry/Immunofluorescence: FoxP3 Antibody [NBP2-58697] - Staining of human cell line PC-3 shows localization to nucleoplasm. Antibody staining is shown in green.](http://images.novusbio.com/fullsize/FoxP3-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-58697-img0001.jpg)
![Flow Cytometry: CD4 Antibody (CE9.1 (Clenoliximab)) - Chimeric [NBP2-52681] - Flow-cytometry using the anti-CD4 research biosimilar antibody Clenoliximab (NBP2-52681) Human lymphocytes were stained with an isotype control (panel A) or the rabbit-chimeric version of Clenoliximab (panel B) at a concentration of 1 ug/ml for 30 mins at RT. After washing, bound antibody was detected using a AF488 conjugated donkey anti-rabbit antibody and cells analysed on a FACSCanto flow-cytometer.](http://images.novusbio.com/fullsize/CD4-Antibody-CE9-1-Clenoliximab-Chimeric-Flow-Cytometry-NBP2-52681-img0001.jpg "Flow Cytometry: CD4 Antibody (CE9.1 (Clenoliximab)) - Chimeric [NBP2-52681] - Flow-cytometry using the anti-CD4 research biosimilar antibody Clenoliximab (NBP2-52681) Human lymphocytes were stained with an isotype control (panel A) or the rabbit-chimeric version of Clenoliximab (panel B) at a concentration of 1 ug/ml for 30 mins at RT. After washing, bound antibody was detected using a AF488 conjugated donkey anti-rabbit antibody and cells analysed on a FACSCanto flow-cytometer.")
![Immunohistochemistry: CD4 Antibody (CE9.1 (Clenoliximab)) [NBP2-75910] - Anti-CD4 staining of formaldehyde fixed paraffin embedded guinea pig skin tissue, at 40x magnification. The human IgG4-chimeric version of CE9.1 (Clenoliximab) (NBP2-75910) was used to stain samples at a concentration of 3 ug/ml.](http://images.novusbio.com/fullsize/CD4-Antibody-CE9-1-Clenoliximab-Immunohistochemistry-NBP2-75910-img0002.jpg "Immunohistochemistry: CD4 Antibody (CE9.1 (Clenoliximab)) [NBP2-75910] - Anti-CD4 staining of formaldehyde fixed paraffin embedded guinea pig skin tissue, at 40x magnification. The human IgG4-chimeric version of CE9.1 (Clenoliximab) (NBP2-75910) was used to stain samples at a concentration of 3 ug/ml.")
![Western Blot: CD4 Antibody (CE9.1 (Clenoliximab)) [NBP2-75910] - Human thyroid tumour samples were resolved on a 15% SDS PAGE gel and blots probed with the human IgG4-chimeric version of CE9.1 (NBP2-75910) at 1.5 ug/ml before detection using an anti-human IgG4 secondary antibody. Protein was detected by chemiluminescence. The expected unmodified running size for CD4 is 51kDa (arrowhead). Here some non-specific bands can also be seen. NBP2-75910 successfully detected CD4 in human thyroid tissue samples.](http://images.novusbio.com/fullsize/CD4-Antibody-CE9-1-Clenoliximab-Western-Blot-NBP2-75910-img0003.jpg)
![Immunohistochemistry: CD4 Antibody (2B7) [NBP3-26682] - Image of CD4 Antibody (2B7) diluted at 1:100 and staining in paraffin-embedded human lymph node tissue performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.](http://images.novusbio.com/fullsize/nbp3-26682_rabbit-cd4-mab-2b7-262202414225214.jpg "Immunohistochemistry: CD4 Antibody (2B7) [NBP3-26682] - Image of CD4 Antibody (2B7) diluted at 1:100 and staining in paraffin-embedded human lymph node tissue performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.")
![Immunohistochemistry: CD4 Antibody (2B7) [NBP3-26682] - Image of CD4 Antibody (2B7) diluted at 1:100 and staining in paraffin-embedded human lymph node tissue performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.](http://images.novusbio.com/fullsize/nbp3-26682_rabbit-cd4-mab-2b7-262202415253330.jpg)
![Western Blot: CD4 Antibody (2B7) [NBP3-26682] - Positive Western Blot detected in Jurkat whole cell lysate. All lanes: CD4 Antibody at 0.8ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 55 KDa Observed band size: 55 KDa](http://images.novusbio.com/fullsize/nbp3-26682_rabbit-cd4-mab-2b7-28220241152515.jpg)
![Immunohistochemistry: STAT4 Antibody (26G2) [NBP3-26300] - Image of STAT4 Antibody (26G2) diluted at 1:100 and staining in paraffin-embedded human testis tissue performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26300_rabbit-stat4-mab-26g2-262202415355717.jpg "Immunohistochemistry: STAT4 Antibody (26G2) [NBP3-26300] - Image of STAT4 Antibody (26G2) diluted at 1:100 and staining in paraffin-embedded human testis tissue performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB.")
![Immunohistochemistry: STAT4 Antibody (26G2) [NBP3-26300] - Image of STAT4 Antibody (26G2) diluted at 1:100 and staining in paraffin-embedded human testis tissue performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26300_rabbit-stat4-mab-26g2-27220248504614.jpg)
![Immunocytochemistry/Immunofluorescence: STAT4 Antibody (26G2) [NBP3-26300] - Staining of HepG2 cell with STAT4 Antibody (26G2) at 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 515-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26300_rabbit-stat4-mab-26g2-282202412475120.jpg)
![Flow Cytometry: CD4 Antibody (13B8.2) - Chimeric [NBP2-52670] - Flow-cytometry using anti-CD4 antibody 13B8.2. Human lymphocytes were stained with an isotype control (panel A) or the rabbit-chimeric version of 13B8.2 (NBP2-52670, panel B) at a concentration of 1 ug/ml for 30 mins at RT. After washing, bound antibody was detected using a AF488 conjugated donkey anti-rabbit antibody and cells analysed on a FACSCanto flow-cytometer.](http://images.novusbio.com/fullsize/CD4-Antibody-13B8-2-Chimeric-Flow-Cytometry-NBP2-52670-img0001.jpg "Flow Cytometry: CD4 Antibody (13B8.2) - Chimeric [NBP2-52670] - Flow-cytometry using anti-CD4 antibody 13B8.2. Human lymphocytes were stained with an isotype control (panel A) or the rabbit-chimeric version of 13B8.2 (NBP2-52670, panel B) at a concentration of 1 ug/ml for 30 mins at RT. After washing, bound antibody was detected using a AF488 conjugated donkey anti-rabbit antibody and cells analysed on a FACSCanto flow-cytometer.")
