| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-52708-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-52662-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-51664SS | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-22118SS | |||
| Azide and BSA Free | NBP2-80587 | |||
![Western Blot: SOX9 Antibody (SN74-09) [NBP2-67690] - Analysis of SOX9 on NIH/3T3 cell lysates with Rabbit anti-SOX9 antibody at 1/500 dilution. Lysates/proteins at 10 ug/Lane. Predicted band size: 56 kDa Observed band size: 70 kDa Exposure time: 30 seconds; 8% 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/SOX9-Antibody-SN74-09-Western-Blot-NBP2-67690-img0010.jpg "Western Blot: SOX9 Antibody (SN74-09) [NBP2-67690] - Analysis of SOX9 on NIH/3T3 cell lysates with Rabbit anti-SOX9 antibody at 1/500 dilution. Lysates/proteins at 10 ug/Lane. Predicted band size: 56 kDa Observed band size: 70 kDa Exposure time: 30 seconds; 8% 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.")
![Immunocytochemistry/Immunofluorescence: SOX9 Antibody (SN74-09) [NBP2-67690] - Staining SOX9 in SW480 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/SOX9-Antibody-SN74-09-Immunocytochemistry-Immunofluorescence-NBP2-67690-img0007.jpg)
![Immunohistochemistry-Paraffin: SOX9 Antibody (SN74-09) [NBP2-67690] - Analysis of paraffin-embedded human lung carcinoma tissue with Rabbit anti-SOX9 antibody washed with ddH2O and PBS, and then probed with the primary antibody 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/SOX9-Antibody-SN74-09-Immunohistochemistry-Paraffin-NBP2-67690-img0017.jpg)
![Flow Cytometry: SOX9 Antibody (SN74-09) [NBP2-67690] - Analysis of Hela cells with SOX9 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/SOX9-Antibody-SN74-09-Flow-Cytometry-NBP2-67690-img0001.jpg)
![Western Blot: SOX9 Antibody (SN74-09) [NBP2-67690] - Analysis of SOX9 on SW480 cell 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/SOX9-Antibody-SN74-09-Western-Blot-NBP2-67690-img0008.jpg)
![Western Blot: SOX9 Antibody (SN74-09) [NBP2-67690] - Analysis of SOX9 on different lysates with Rabbit anti-SOX9 antibody at 1/500 dilution.Lane 1: SW480 cell lysateLane 2: A431 cell lysateLysates/proteins at 10 ug/Lane.Predicted band size: 56 kDaObserved band size: 70 kDaExposure time: 2 minutes;10% 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/SOX9-Antibody-SN74-09-Western-Blot-NBP2-67690-img0009.jpg)
![Immunocytochemistry/Immunofluorescence: SOX9 Antibody (SN74-09) [NBP2-67690] - Staining SOX9 in MCF-7 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/SOX9-Antibody-SN74-09-Immunocytochemistry-Immunofluorescence-NBP2-67690-img0002.jpg)
![Immunohistochemistry-Paraffin: SOX9 Antibody (SN74-09) [NBP2-67690] - Analysis of paraffin-embedded human breast carcinoma tissue using anti-SOX9 antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/SOX9-Antibody-SN74-09-Immunohistochemistry-Paraffin-NBP2-67690-img0003.jpg)
![Immunohistochemistry-Paraffin: SOX9 Antibody (SN74-09) [NBP2-67690] - Analysis of paraffin-embedded human tonsil tissue using anti-SOX9 antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/SOX9-Antibody-SN74-09-Immunohistochemistry-Paraffin-NBP2-67690-img0004.jpg)
![Immunohistochemistry-Paraffin: SOX9 Antibody (SN74-09) [NBP2-67690] - Analysis of paraffin-embedded mouse colon tissue using anti-SOX9 antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/SOX9-Antibody-SN74-09-Immunohistochemistry-Paraffin-NBP2-67690-img0005.jpg)
![Immunohistochemistry-Paraffin: SOX9 Antibody (SN74-09) [NBP2-67690] - Analysis of paraffin-embedded mouse spleen tissue using anti-SOX9 antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/SOX9-Antibody-SN74-09-Immunohistochemistry-Paraffin-NBP2-67690-img0006.jpg)
![Immunohistochemistry-Paraffin: SOX9 Antibody (SN74-09) [NBP2-67690] - Analysis of paraffin-embedded human breast carcinoma tissue with Rabbit anti-SOX9 antibody washed with ddH2O and PBS, and then probed with the primary antibody at 1/50 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/SOX9-Antibody-SN74-09-Immunohistochemistry-Paraffin-NBP2-67690-img0011.jpg)
![Immunohistochemistry-Paraffin: SOX9 Antibody (SN74-09) [NBP2-67690] - Analysis of paraffin-embedded human thyroid tissue with Rabbit anti-SOX9 antibody washed with ddH2O and PBS, and then probed with the primary antibody at 1/50 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/SOX9-Antibody-SN74-09-Immunohistochemistry-Paraffin-NBP2-67690-img0012.jpg)
![Immunohistochemistry-Paraffin: SOX9 Antibody (SN74-09) [NBP2-67690] - Analysis of paraffin-embedded human breast tissue with Rabbit anti-SOX9 antibody washed with ddH2O and PBS, and then probed with the primary antibody at 1/50 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/SOX9-Antibody-SN74-09-Immunohistochemistry-Paraffin-NBP2-67690-img0013.jpg)
![Immunohistochemistry-Paraffin: SOX9 Antibody (SN74-09) [NBP2-67690] - Analysis of paraffin-embedded human small intestine tissue with Rabbit anti-SOX9 antibody washed with ddH2O and PBS, and then probed with the primary antibody at 1/50 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/SOX9-Antibody-SN74-09-Immunohistochemistry-Paraffin-NBP2-67690-img0014.jpg)
![Immunohistochemistry-Paraffin: SOX9 Antibody (SN74-09) [NBP2-67690] - Analysis of paraffin-embedded human prostate carcinoma tissue with Rabbit anti-SOX9 antibody washed with ddH2O and PBS, and then probed with the primary antibody 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/SOX9-Antibody-SN74-09-Immunohistochemistry-Paraffin-NBP2-67690-img0015.jpg)
![Immunohistochemistry-Paraffin: SOX9 Antibody (SN74-09) [NBP2-67690] - Analysis of paraffin-embedded human stomach carcinoma tissue with Rabbit anti-SOX9 antibody washed with ddH2O and PBS, and then probed with the primary antibody at 1/50 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/SOX9-Antibody-SN74-09-Immunohistochemistry-Paraffin-NBP2-67690-img0016.jpg)
![Western Blot: HES-1 Antibody (SC06-21) [NBP2-67642] - Analysis of Hes1 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 at 1:5,000 dilution was used for 1 hour at room temperature. Positive control: Lane 1: SiHa cell lysate Lane 2: SK-Br-3 cell lysate](http://images.novusbio.com/fullsize/HES-1-Antibody-SC06-21-Western-Blot-NBP2-67642-img0005.jpg "Western Blot: HES-1 Antibody (SC06-21) [NBP2-67642] - Analysis of Hes1 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 at 1:5,000 dilution was used for 1 hour at room temperature. Positive control: Lane 1: SiHa cell lysate Lane 2: SK-Br-3 cell lysate")
![Immunocytochemistry/Immunofluorescence: HES-1 Antibody (SC06-21) [NBP2-67642] - Staining Hes1 in Hela 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/HES-1-Antibody-SC06-21-Immunocytochemistry-Immunofluorescence-NBP2-67642-img0003.jpg)
![Immunohistochemistry-Paraffin: HES-1 Antibody (SC06-21) [NBP2-67642] - Analysis of paraffin-embedded human breast carcinoma tissue with Rabbit anti-HES-1 antibody washed with ddH2O and PBS, and then probed with the primary antibody at 1/400 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/HES-1-Antibody-SC06-21-Immunohistochemistry-Paraffin-NBP2-67642-img0007.jpg)
![Flow Cytometry: HES-1 Antibody (SC06-21) [NBP2-67642] - Analysis of sh-sy-5y cells with Hes1 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/HES-1-Antibody-SC06-21-Flow-Cytometry-NBP2-67642-img0001.jpg)
![Immunocytochemistry/Immunofluorescence: HES-1 Antibody (SC06-21) [NBP2-67642] - Staining Hes1 in 293 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/HES-1-Antibody-SC06-21-Immunocytochemistry-Immunofluorescence-NBP2-67642-img0002.jpg)
![Immunohistochemistry-Paraffin: HES-1 Antibody (SC06-21) [NBP2-67642] - Analysis of paraffin-embedded mouse brain tissue using anti-Hes1 antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/HES-1-Antibody-SC06-21-Immunohistochemistry-Paraffin-NBP2-67642-img0004.jpg)
![<b>Biological Strategies Validation. </b>Immunohistochemistry-Paraffin: HES-1 Antibody (SC06-21) [NBP2-67642] - Analysis of paraffin-embedded rat brain tissue using anti-Hes1 antibody. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) 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/HES-1-Antibody-SC06-21-Immunohistochemistry-Paraffin-NBP2-67642-img0006.jpg)
![Western Blot: NGFR/TNFRSF16/p75NTR Antibody (SA39-02) [NBP2-67296] - Analysis of p75 NGF Receptor on PC-12 cell 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 1:200,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/NGFR-TNFRSF16-p75NTR-Antibody-SA39-02-Western-Blot-NBP2-67296-img0011.jpg "Western Blot: NGFR/TNFRSF16/p75NTR Antibody (SA39-02) [NBP2-67296] - Analysis of p75 NGF Receptor on PC-12 cell 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 1:200,000 dilution was used for 1 hour at room temperature.")
![Immunocytochemistry/Immunofluorescence: NGFR/TNFRSF16/p75NTR Antibody (SA39-02) [NBP2-67296] - Staining NGFR p75 in N2A 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/NGFR-TNFRSF16-p75NTR-Antibody-SA39-02-Immunocytochemistry-Immunofluorescence-NBP2-67296-img0005.jpg)
![<b>Biological Strategies Validation. </b>Immunohistochemistry-Paraffin: NGFR/TNFRSF16/p75NTR Antibody (SA39-02) [NBP2-67296] - Rat uterus tissue using anti-p75 NGF Receptor 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/NGFR-TNFRSF16-p75NTR-Antibody-SA39-02-Immunohistochemistry-Paraffin-NBP2-67296-img0009.jpg)
![Western Blot: NGFR/TNFRSF16/p75NTR Antibody (SA39-02) [NBP2-67296] - Western blot analysis of NGFR/TNFRSF16/p75NTR on skeletal muscle 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 temperatur](http://images.novusbio.com/fullsize/NGFR-TNFRSF16-p75NTR-Antibody-SA39-02-Western-Blot-NBP2-67296-img0010.jpg)
![Immunocytochemistry/Immunofluorescence: NGFR/TNFRSF16/p75NTR Antibody (SA39-02) [NBP2-67296] - Staining NGFR p75 in Hela 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/NGFR-TNFRSF16-p75NTR-Antibody-SA39-02-Immunocytochemistry-Immunofluorescence-NBP2-67296-img0001.jpg)
![<b>Biological Strategies Validation. </b>Immunohistochemistry-Paraffin: NGFR/TNFRSF16/p75NTR Antibody (SA39-02) [NBP2-67296] - Analysis of mouse uterus tissue using anti-p75 NGF Receptor 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/NGFR-TNFRSF16-p75NTR-Antibody-SA39-02-Immunohistochemistry-Paraffin-NBP2-67296-img0006.jpg)
![<b>Biological Strategies Validation. </b>Immunohistochemistry-Paraffin: NGFR/TNFRSF16/p75NTR Antibody (SA39-02) [NBP2-67296] - Human tonsil tissue using anti-p75 NGF Receptor 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/NGFR-TNFRSF16-p75NTR-Antibody-SA39-02-Immunohistochemistry-Paraffin-NBP2-67296-img0007.jpg)
![<b>Biological Strategies Validation. </b>Immunohistochemistry-Paraffin: NGFR/TNFRSF16/p75NTR Antibody (SA39-02) [NBP2-67296] - Human uterus tissue using anti-p75 NGF Receptor 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/NGFR-TNFRSF16-p75NTR-Antibody-SA39-02-Immunohistochemistry-Paraffin-NBP2-67296-img0008.jpg)
![Flow Cytometry: Integrin beta 1/CD29 Antibody (K20) [NBP2-52708] - Flow-cytometry using anti-CD29 antibody K20 (NBP2-52708) Human leukocytes were stained with an isotype control (panel A) or the rabbit-chimeric version of K20 (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/Integrin-beta-1-CD29-Antibody-K20-NBP2-52708-img0001.jpg "Flow Cytometry: Integrin beta 1/CD29 Antibody (K20) [NBP2-52708] - Flow-cytometry using anti-CD29 antibody K20 (NBP2-52708) Human leukocytes were stained with an isotype control (panel A) or the rabbit-chimeric version of K20 (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.")
![Flow Cytometry: CD19 Antibody (HD37) - Chimeric [NBP2-52662] - Flow-cytometry using anti-CD19 antibody HD37. Human lymphocytes were stained with an isotype control (panel A) or the rabbit-chimeric version of HD37 (NBP2-52662, 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/CD19-Antibody-HD37-Chimeric-Flow-Cytometry-NBP2-52662-img0001.jpg "Flow Cytometry: CD19 Antibody (HD37) - Chimeric [NBP2-52662] - Flow-cytometry using anti-CD19 antibody HD37. Human lymphocytes were stained with an isotype control (panel A) or the rabbit-chimeric version of HD37 (NBP2-52662, 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.")
![Western Blot: Exonuclease 1 Antibody [NBP2-16391] - Sample (50 ug of whole cell lysate) A: mouse thymus, 7. 5% SDS PAGE gel, diluted at 1:1000.](http://images.novusbio.com/fullsize/Exonuclease-1-Antibody-Western-Blot-NBP2-16391-img0002.jpg "Western Blot: Exonuclease 1 Antibody [NBP2-16391] - Sample (50 ug of whole cell lysate) A: mouse thymus, 7. 5% SDS PAGE gel, diluted at 1:1000.")
![Immunocytochemistry/Immunofluorescence: Exonuclease 1 Antibody [NBP2-16391] - Analysis of paraformaldehyde-fixed HeLa, using antibody at 1:500 dilution.](http://images.novusbio.com/fullsize/Exonuclease-1-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-16391-img0003.jpg)
![Western Blot: OCT4 Antibody (7E7) [NBP1-51664] - Analysis using OCT4 mouse mAb against NTERA-2 cell lysate.](http://images.novusbio.com/fullsize/OCT4-Antibody-7E7-Western-Blot-NBP1-51664-img0007.jpg "Western Blot: OCT4 Antibody (7E7) [NBP1-51664] - Analysis using OCT4 mouse mAb against NTERA-2 cell lysate.")
![Immunocytochemistry/Immunofluorescence: OCT4 Antibody (7E7) [NBP1-51664] - Analysis of NTERA-2 cells using OCT4 mouse mAb (green). Actin filaments have been labeled with Alexa Fluor-555 phalloidin (red).](http://images.novusbio.com/fullsize/OCT4-Antibody-7E7-Immunocytochemistry-Immunofluorescence-NBP1-51664-img0008.jpg)
![Flow Cytometry: OCT4 Antibody (7E7) [NBP1-51664] - Flow cytometric analysis of Jurket cells using OCT4 mouse mAb (green) and negative control (purple).](http://images.novusbio.com/fullsize/OCT4-Antibody-7E7-Flow-Cytometry-NBP1-51664-img0005.jpg)
![Immunocytochemistry/Immunofluorescence: OCT4 Antibody (7E7) [NBP1-51664] - Analysis of NTERA-2 cells using OCT4 mouse mAb (green). Actin filaments have been labeled with Alexa Fluor-555 phalloidin (red).](http://images.novusbio.com/fullsize/OCT4-Antibody-7E7-Immunocytochemistry-Immunofluorescence-NBP1-51664-img0006.jpg)
![Western Blot: Aurora A Antibody (1F8) [NBP2-22118] - Analysis using Aurora A mouse mAb against HEK293 (1), Sw620 (2), MCF-7 (3), Jurkat (4), Hela (5), HepG2 (6), Cos7 (7) and PC-12 (8) cell lysates.](http://images.novusbio.com/fullsize/Aurora-A-Antibody-1F8-Western-Blot-NBP2-22118-img0002.jpg "Western Blot: Aurora A Antibody (1F8) [NBP2-22118] - Analysis using Aurora A mouse mAb against HEK293 (1), Sw620 (2), MCF-7 (3), Jurkat (4), Hela (5), HepG2 (6), Cos7 (7) and PC-12 (8) cell lysates.")
![Immunocytochemistry/Immunofluorescence: Aurora A Antibody (1F8) [NBP2-22118] - Analysis of Hela cells using Aurora A mouse mAb (green). DRAQ5 fluorescent DNA dye (blue).](http://images.novusbio.com/fullsize/Aurora-A-Antibody-1F8-Immunocytochemistry-Immunofluorescence-NBP2-22118-img0004.jpg)
![Flow Cytometry: Aurora A Antibody (1F8) [NBP2-22118] - Analysis of K562 cells using Aurora A mouse mAb (green) and negative control (purple).](http://images.novusbio.com/fullsize/Aurora-A-Antibody-1F8-Flow-Cytometry-NBP2-22118-img0003.jpg)
![ELISA: Aurora A Antibody (1F8) [NBP2-22118] - Red: Control Antigen (100ng), Purple: Antigen (10ng), Green: Antigen (50ng), Blue: Antigen (100ng).](http://images.novusbio.com/fullsize/Aurora-A-Antibody-1F8-ELISA-NBP2-22118-img0001.jpg)
![Western Blot: UNG Antibody [NBP1-49985] - Western blot shows lysates of HeLa human cervical epithelial carcinoma parental cell line and UNG knockout (KO) HeLa cell line. PVDF membrane was probed with 1:2000 of Rabbit Anti-Human UNG Polyclonal Antibody (Catalog # NBP1-49985) followed by HRP-conjugated Anti-Rabbit IgG Secondary Antibody (Catalog #HAF008). Specific band was detected for UNG at approximately 38 kDa (as indicated) in the parental HeLa cell line, but is not detectable in the knockout HeLa cell line. This experiment was conducted under reducing conditions.](http://images.novusbio.com/fullsize/UNG-Antibody-Knockdown-Validated-NBP1-49985-img0003.jpg "<b>Genetic Strategies Validation. </b>Western Blot: UNG Antibody [NBP1-49985] - Western blot shows lysates of HeLa human cervical epithelial carcinoma parental cell line and UNG knockout (KO) HeLa cell line. PVDF membrane was probed with 1:2000 of Rabbit Anti-Human UNG Polyclonal Antibody (Catalog # NBP1-49985) followed by HRP-conjugated Anti-Rabbit IgG Secondary Antibody (Catalog #HAF008). Specific band was detected for UNG at approximately 38 kDa (as indicated) in the parental HeLa cell line, but is not detectable in the knockout HeLa cell line. This experiment was conducted under reducing conditions.")
![<b>Genetic Strategies Validation. </b>Western Blot: UNG Antibody [NBP1-49985] - Detection of Human UNG by Western Blot and Immunoprecipitation. Samples: Whole cell lysate from HeLa (5, 15 and 50 mcg for WB; 1 mg for IP, 20% of IP loaded) and 293T (T; 50 mcg) cells. Antibodies: Affinity purified rabbit anti-UNG antibody used for WB at 0.1 mcg/ml (A) and 1 mcg/ml (B) and used for IP at 3 mcg/mg lysate. UNG was successfully immunoprecipitated by rabbit anti-UNG antibody which recognizes an upstream epitope. For blotting immunoprecipitated UNG was used. Detection: Chemiluminescence with exposure times of 3 minutes (A) and 30 seconds (B).](http://images.novusbio.com/fullsize/UNG-Antibody-Western-Blot-NBP1-49985-img0002.jpg)
![Western Blot: hnRNP K Antibody [NBP2-24532] - analysis of hnRNPK in K562 cell lysate in the 1) absence and2) presence of immunizing peptide and 3) NIH 3T3 cell lysate using this antibody. I goat anti-rabbit Ig HRP secondary antibody and PicoTect ECL substrate solution were used for this test.](http://images.novusbio.com/fullsize/hnRNP-K-Antibody-Western-Blot-NBP2-24532-img0001.jpg "Western Blot: hnRNP K Antibody [NBP2-24532] - analysis of hnRNPK in K562 cell lysate in the 1) absence and2) presence of immunizing peptide and 3) NIH 3T3 cell lysate using this antibody. I goat anti-rabbit Ig HRP secondary antibody and PicoTect ECL substrate solution were used for this test.")
![Immunohistochemistry-Paraffin: hnRNP K Antibody [NBP2-24532] - Formalin-fixed, paraffin-embedded human adrenal tissue probed with hnRNPK antibody at 5 ug/ml.](http://images.novusbio.com/fullsize/hnRNP-K-Antibody-Immunohistochemistry-Paraffin-NBP2-24532-img0005.jpg)
![Immunohistochemistry-Paraffin: hnRNP K Antibody [NBP2-24532] - Formalin-fixed, paraffin-embedded human thymus probed with hnRNPK antibody at 5 ug/ml.](http://images.novusbio.com/fullsize/hnRNP-K-Antibody-Immunohistochemistry-Paraffin-NBP2-24532-img0004.jpg)
![Simple Western: hnRNP K Antibody [NBP2-24532] - Simple Western lane view shows a specific band for hnRNP K in 0.5 mg/ml of NIH-3T3 lysate. This experiment was performed under reducing conditions using the 12-230 kDa separation system.](http://images.novusbio.com/fullsize/hnRNP-K-Antibody-Simple-Western-NBP2-24532-img0006.jpg)
![Western Blot: ZIC3 Antibody [NBP1-33207] - Sample (30 ug of whole cell lysate) A: Hep G2 10% SDS PAGE; antibody diluted at 1:500](http://images.novusbio.com/fullsize/ZIC3-Antibody-Western-Blot-NBP1-33207-img0001.jpg "Western Blot: ZIC3 Antibody [NBP1-33207] - Sample (30 ug of whole cell lysate) A: Hep G2 10% SDS PAGE; antibody diluted at 1:500")
![Immunocytochemistry/Immunofluorescence: ZIC3 Antibody [NBP1-33207] - Analysis of paraformaldehyde-fixed Human ESC, using antibody at 1:100 dilution.](http://images.novusbio.com/fullsize/ZIC3-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-33207-img0002.jpg)
![ZIC3 antibody [N3C3] detects ZIC3 protein expression by immunohistochemical analysis.Sample: Frozen sectioned E13.5 Rat brain. Green: ZIC3 protein stained by ZIC3 antibody [N3C3] (NBP1-33207) diluted at 1:250.Red: beta Tubulin 3/ TUJ1, a mature neuron marker, stained by beta Tubulin 3/ TUJ1 antibody [GT11710] diluted at 1:500.Blue: Fluoroshield with DAPI .](http://images.novusbio.com/fullsize/nbp1-33207_rabbit-polyclonal-zic3-antibody-immunohistochemistry-frozen-26112025198365.jpg)
![Western Blot: SUCLG2 Antibody [NBP1-32521] - Wild-type (WT) and SUCLG2 knockout (KO) 293T cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with SUCLG2 antibody diluted at 1:500. HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/SUCLG2-Antibody-Western-Blot-NBP1-32521-img0013.jpg "<b>Genetic Strategies Validation. </b>Western Blot: SUCLG2 Antibody [NBP1-32521] - Wild-type (WT) and SUCLG2 knockout (KO) 293T cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with SUCLG2 antibody diluted at 1:500. HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.")
![<b>Genetic Strategies Validation. </b>Immunocytochemistry/Immunofluorescence: SUCLG2 Antibody [NBP1-32521] - HeLa cells were fixed in ice-cold MeOH for 5 min. Green: SUCLG2 protein stained by SUCLG2 antibody diluted at 1:500. Blue: Hoechst 33342 staining. Scale bar = 10 um.](http://images.novusbio.com/fullsize/SUCLG2-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-32521-img0012.jpg)
![Immunohistochemistry-Paraffin: SUCLG2 Antibody [NBP1-32521] - Paraffin-embedded hepatoma. SUCLG2 antibody dilution: 1:500](http://images.novusbio.com/fullsize/SUCLG2-Antibody-Immunohistochemistry-Paraffin-NBP1-32521-img0008.jpg)
![Western Blot: SUCLG2 Antibody [NBP1-32521] - A: mouse liver 10% SDS PAGE diluted at 1:10000](http://images.novusbio.com/fullsize/SUCLG2-Antibody-Western-Blot-NBP1-32521-img0010.jpg)
![Western Blot: SUCLG2 Antibody [NBP1-32521] - A: 293T B: A431 C: H1299 D: HeLa S3 E: Hep G2 F: MOLT4 G: Raji 10% SDS PAGE diluted at 1:1000](http://images.novusbio.com/fullsize/SUCLG2-Antibody-Western-Blot-NBP1-32521-img0011.jpg)
