| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-24858SS | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | MAB35062-SP | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-44249SS | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB100-1922SS | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB100-56498SS | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-87885-25ul | |||
![Western Blot: alpha Tubulin Antibody (PSH02-94) [NBP3-33139] - Western blot analysis of alpha Tubulin on different lysates with Rabbit anti-alpha Tubulin antibody (NBP3-33139) at 1/5,000 dilution. Lane 1: HeLa cell lysate Lane 2: PC-12 cell lysate Lane 3: NIH/3T3 cell lysate Lane 4: Daudi cell lysate Lane 5: Jurkat cell lysate Lane 6: A431 cell lysate Lane 7: K-562 cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 50 kDa Observed band size: 50 kDa Exposure time: 1 minutes 2 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 (NBP3-33139) at 1/5,000 dilution was used in 5% NFDM/TBST at 4C overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-33139_rabbit-alpha-tubulin-mab-psh02-94-28820241423313.jpg "Western Blot: alpha Tubulin Antibody (PSH02-94) [NBP3-33139] - Western blot analysis of alpha Tubulin on different lysates with Rabbit anti-alpha Tubulin antibody (NBP3-33139) at 1/5,000 dilution. Lane 1: HeLa cell lysate Lane 2: PC-12 cell lysate Lane 3: NIH/3T3 cell lysate Lane 4: Daudi cell lysate Lane 5: Jurkat cell lysate Lane 6: A431 cell lysate Lane 7: K-562 cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 50 kDa Observed band size: 50 kDa Exposure time: 1 minutes 2 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 (NBP3-33139) at 1/5,000 dilution was used in 5% NFDM/TBST at 4C overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: alpha Tubulin Antibody (PSH02-94) [NBP3-33139] - Immunohistochemical analysis of paraffin-embedded human tonsil tissue with Rabbit anti-alpha Tubulin antibody (NBP3-33139) 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 (NBP3-33139) 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/nbp3-33139_rabbit-alpha-tubulin-mab-psh02-94-29820241435223.jpg)
![Immunocytochemistry/ Immunofluorescence: alpha Tubulin Antibody (PSH02-94) [NBP3-33139] - Immunocytochemistry analysis of Daudi cells labeling alpha Tubulin with Rabbit anti-alpha Tubulin antibody (NBP3-33139) at 1/500 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-alpha Tubulin antibody (NBP3-33139) at 1/500 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/nbp3-33139_rabbit-alpha-tubulin-mab-psh02-94-29202410484898.jpg)
![Flow Cytometry: alpha Tubulin Antibody (PSH02-94) [NBP3-33139] - Flow cytometric analysis of HeLa cells labeling alpha Tubulin. Cells were fixed and permeabilized. Then stained with the primary antibody (NBP3-33139, 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/nbp3-33139_rabbit-alpha-tubulin-mab-psh02-94-39202488464.jpg)
![Western Blot: PMP70 Antibody (PSH03-27) [NBP3-32834] - Western blot analysis of PMP70 on different lysates with Rabbit anti-PMP70 antibody (NBP3-32834) at 1/2,000 dilution. Lane 1: HepG2 cell lysate (20 ug/Lane) Lane 2: 293T cell lysate (20 ug/Lane) Lane 3: A431 cell lysate (20 ug/Lane) Lane 4: Caco-2 cell lysate (20 ug/Lane) Lane 5: SH-SY5Y cell lysate (20 ug/Lane) Lane 6: Human liver tissue lysate (40 ug/Lane) Lane 7: Mouse liver tissue lysate (40 ug/Lane) Lysates/proteins at 10 ug/Lane. Predicted band size: 76 kDa Observed band size: 70 kDa Exposure time: 24 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 (NBP3-32834) at 1/2,000 dilution was used in 5% NFDM/TBST at 4C overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32834_rabbit-pmp70-mab-psh03-27-288202412461658.jpg "Western Blot: PMP70 Antibody (PSH03-27) [NBP3-32834] - Western blot analysis of PMP70 on different lysates with Rabbit anti-PMP70 antibody (NBP3-32834) at 1/2,000 dilution. Lane 1: HepG2 cell lysate (20 ug/Lane) Lane 2: 293T cell lysate (20 ug/Lane) Lane 3: A431 cell lysate (20 ug/Lane) Lane 4: Caco-2 cell lysate (20 ug/Lane) Lane 5: SH-SY5Y cell lysate (20 ug/Lane) Lane 6: Human liver tissue lysate (40 ug/Lane) Lane 7: Mouse liver tissue lysate (40 ug/Lane) Lysates/proteins at 10 ug/Lane. Predicted band size: 76 kDa Observed band size: 70 kDa Exposure time: 24 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 (NBP3-32834) at 1/2,000 dilution was used in 5% NFDM/TBST at 4C overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: PMP70 Antibody (PSH03-27) [NBP3-32834] - Immunohistochemical analysis of paraffin-embedded human kidney tissue with Rabbit anti-PMP70 antibody (NBP3-32834) at 1/500 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 (NBP3-32834) at 1/500 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/nbp3-32834_rabbit-pmp70-mab-psh03-27-298202414333688.jpg)
![Immunocytochemistry/ Immunofluorescence: PMP70 Antibody (PSH03-27) [NBP3-32834] - Immunocytochemistry analysis of HepG2 cells labeling PMP70 with Rabbit anti-PMP70 antibody (NBP3-32834) 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-PMP70 antibody (NBP3-32834) 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/nbp3-32834_rabbit-pmp70-mab-psh03-27-29202410334056.jpg)
![Flow Cytometry: PMP70 Antibody (PSH03-27) [NBP3-32834] - Flow cytometric analysis of NIH/3T3 cells labeling PMP70. Cells were fixed and permeabilized. Then stained with the primary antibody (NBP3-32834, 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/nbp3-32834_rabbit-pmp70-mab-psh03-27-2920241637212.jpg)
![Western Blot: PA28 Activator beta Subunit/PSME2 Antibody (PSH0-10) [NBP3-32868] - Western blot analysis of PA28 Activator beta Subunit/PSME2 on different lysates with Rabbit anti-PA28 Activator beta Subunit/PSME2 antibody (NBP3-32868) at 1/1,000 dilution. Lane 1: PC-12 cell lysate (10 ug/Lane) Lane 2: 293T cell lysate (10 ug/Lane) Lane 3: Mouse liver tissue lysate (20 ug/Lane) Lane 4: Rat thymus tissue lysate (20 ug/Lane) Lane 5: MCF-7 cell lysate (10 ug/Lane) Lane 6: PC-3 cell lysate (10 ug/Lane) Predicted band size: 27 kDa Observed band size: 30 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 (NBP3-32868) 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/nbp3-32868_rabbit-pa28-activator-beta-subunit-psme2-mab-psh0-10-288202412461650.jpg "Western Blot: PA28 Activator beta Subunit/PSME2 Antibody (PSH0-10) [NBP3-32868] - Western blot analysis of PA28 Activator beta Subunit/PSME2 on different lysates with Rabbit anti-PA28 Activator beta Subunit/PSME2 antibody (NBP3-32868) at 1/1,000 dilution. Lane 1: PC-12 cell lysate (10 ug/Lane) Lane 2: 293T cell lysate (10 ug/Lane) Lane 3: Mouse liver tissue lysate (20 ug/Lane) Lane 4: Rat thymus tissue lysate (20 ug/Lane) Lane 5: MCF-7 cell lysate (10 ug/Lane) Lane 6: PC-3 cell lysate (10 ug/Lane) Predicted band size: 27 kDa Observed band size: 30 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 (NBP3-32868) 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: PA28 Activator beta Subunit/PSME2 Antibody (PSH0-10) [NBP3-32868] - Immunohistochemical analysis of paraffin-embedded rat stomach tissue with Rabbit anti-PA28 Activator beta Subunit/PSME2 antibody (NBP3-32868) at 1/4,000 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 (NBP3-32868) at 1/4,000 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/nbp3-32868_rabbit-pa28-activator-beta-subunit-psme2-mab-psh0-10-298202414304129.jpg)
![Immunocytochemistry/ Immunofluorescence: PA28 Activator beta Subunit/PSME2 Antibody (PSH0-10) [NBP3-32868] - Immunocytochemistry analysis of Hela cells labeling PA28 Activator beta Subunit/PSME2 with Rabbit anti-PA28 Activator beta Subunit/PSME2 antibody (NBP3-32868) at 1/100 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-PA28 Activator beta Subunit/PSME2 antibody (NBP3-32868) at 1/100 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/nbp3-32868_rabbit-pa28-activator-beta-subunit-psme2-mab-psh0-10-29202410234250.jpg)
![Flow Cytometry: PA28 Activator beta Subunit/PSME2 Antibody (PSH0-10) [NBP3-32868] - Flow cytometric analysis of Hela cells labeling PA28 Activator beta Subunit/PSME2. Cells were fixed and permeabilized. Then stained with the primary antibody (NBP3-32868, 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/nbp3-32868_rabbit-pa28-activator-beta-subunit-psme2-mab-psh0-10-29202416453262.jpg)
![Western Blot: ALDH5A1 Antibody [NBP1-32970] - Sample (30 ug of whole cell lysate) A: A431 7. 5% SDS PAGE; antibody diluted at 1:1000.](http://images.novusbio.com/fullsize/ALDH5A1-Antibody-Western-Blot-NBP1-32970-img0005.jpg "Western Blot: ALDH5A1 Antibody [NBP1-32970] - Sample (30 ug of whole cell lysate) A: A431 7. 5% SDS PAGE; antibody diluted at 1:1000.")
![Immunocytochemistry/Immunofluorescence: ALDH5A1 Antibody [NBP1-32970] - Analysis of methanol-fixed A431, using antibody at 1:500 dilution.](http://images.novusbio.com/fullsize/ALDH5A1-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-32970-img0002.jpg)
![Immunohistochemistry-Paraffin: ALDH5A1 Antibody [NBP1-32970] - ALDH5A1 antibody detects ALDH5A1 protein at mitochondria in mouse liver by immunohistochemical analysis. Sample: Paraffin-embedded mouse liver. ALDH5A1 antibody diluted at 1:500.](http://images.novusbio.com/fullsize/ALDH5A1-Antibody-Immunohistochemistry-Paraffin-NBP1-32970-img0006.jpg)
![Western Blot: ALDH5A1 Antibody [NBP1-32970] - Sample (20 ug of whole cell lysate) A: mouse brain 7. 5% SDS PAGE; antibody diluted at 1:5000.](http://images.novusbio.com/fullsize/ALDH5A1-Antibody-Western-Blot-NBP1-32970-img0004.jpg)
![Immunohistochemistry-Paraffin: ALDH5A1 Antibody [NBP1-32970] - Paraffin-embedded A549 xenograft, using antibody at 1:500 dilution.](http://images.novusbio.com/fullsize/ALDH5A1-Antibody-Immunohistochemistry-Paraffin-NBP1-32970-img0003.jpg)
![Western Blot: IL-33 Antibody [NBP2-24858] - Analysis of IL-33 using IL-33 polyclonal antibody. HUVEC cell lysate probed with IL-33 antibody at 1 ug/ml in the 1) absence and 2) presence of immunizing peptide.](http://images.novusbio.com/fullsize/IL-33-Antibody-Western-Blot-NBP2-24858-img0003.jpg "Western Blot: IL-33 Antibody [NBP2-24858] - Analysis of IL-33 using IL-33 polyclonal antibody. HUVEC cell lysate probed with IL-33 antibody at 1 ug/ml in the 1) absence and 2) presence of immunizing peptide.")
![Simple Western: IL-33 Antibody [NBP2-24858] - Lane view shows a specific band for IL-33 in 0.05 mg/ml of Jurkat lysate. This experiment was performed under reducing conditions using the 12-230 kDa separation system.](http://images.novusbio.com/fullsize/IL-33-Antibody-Simple-Western-NBP2-24858-img0002.jpg)
![Western Blot: Cytokeratin 19 Antibody (963410) [MAB35062] - Western blot detection of Cytokeratin 19 (clone 963410), catalog number MAB35062, in HT-29, ZR-75, DU145 and MCF-7 cell lysates at a dilution of 0.25 ug/ml.](http://images.novusbio.com/fullsize/Cytokeratin-19-Antibody-963410-Western-Blot-MAB35062-img0003.jpg "Western Blot: Cytokeratin 19 Antibody (963410) [MAB35062] - Western blot detection of Cytokeratin 19 (clone 963410), catalog number MAB35062, in HT-29, ZR-75, DU145 and MCF-7 cell lysates at a dilution of 0.25 ug/ml.")
![Immunohistochemistry: Cytokeratin 19 Antibody (963410) [MAB35062] - Cytokeratin 19 was detected in immersion fixed paraffin-embedded sections of human breast cancer using Cytokeratin 19 (963410) Monoclonal Antibody at 5 ug/ml. Tissue was stained using Mouse IgG VisUCyte HRP Polymer Antibody (brown) and counterstained with hematoxylin (blue). Specific staining was localized to cell surface in cancer cells.](http://images.novusbio.com/fullsize/Cytokeratin-19-Antibody-963410-Immunohistochemistry-MAB35062-img0006.jpg)
![Western Blot: CD133 Antibody [NBP2-44249] - Total mouse placenta protein was separated on a 7.5% gel by SDS-PAGE, transferred to PVDF membrane and blocked in 5% non-fat milk in TBST. The membrane was probed with 2.0 mg/ml anti-mCD133 in 1% milk and detected with an anti-rabbit HRP secondary antibody using chemiluminescence.](http://images.novusbio.com/fullsize/CD133-Antibody-Western-Blot-NBP2-44249-img0001.jpg "Western Blot: CD133 Antibody [NBP2-44249] - Total mouse placenta protein was separated on a 7.5% gel by SDS-PAGE, transferred to PVDF membrane and blocked in 5% non-fat milk in TBST. The membrane was probed with 2.0 mg/ml anti-mCD133 in 1% milk and detected with an anti-rabbit HRP secondary antibody using chemiluminescence.")
![Immunocytochemistry/Immunofluorescence: CD133 Antibody [NBP2-44249] - NIH/3T3 cells were fixed for 10 minutes using 10% formalin and then permeabilized for 5 minutes using 1X TBS + 0.5% Triton X-100. The cells were incubated with anti-mCD133 (M30) (NBP2-44249) at a 1:200 dilution overnight at 4C and detected with an anti-rabbit DyLight 488 (Green) at a 1:500 dilution. Alpha tubulin was used as a co-stain at a 1:1000 dilution and detected with an anti-mouse DyLight 550 (Red) at a 1:500 dilution. Nuclei were counterstained with DAPI (Blue). Cells were imaged using a 40X objective.](http://images.novusbio.com/fullsize/CD133-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-44249-img0002.jpg)
![Western Blot: Tubby Antibody [NB100-1922] - Detection of tub-1 (GFP complex) using NB 100-1922. Tub-1 (nr2004) was used as a negative control.](http://images.novusbio.com/fullsize/Tubby-Antibody-Western-Blot-NB100-1922-img0004.jpg "Western Blot: Tubby Antibody [NB100-1922] - Detection of tub-1 (GFP complex) using NB 100-1922. Tub-1 (nr2004) was used as a negative control.")
![Western Blot: Somatostatin R5/SSTR5 Antibody [NB100-56498] - Analysis of Somatostatin R5/SSTR5 in human pancreas lysate in the 1) absence and 2) presence of immunizing peptide using Somatostatin Receptor 5 antibody at 0.25 ug/ml.](http://images.novusbio.com/fullsize/Somatostatin-R5-SSTR5-Antibody-Western-Blot-NB100-56498-img0009.jpg "Western Blot: Somatostatin R5/SSTR5 Antibody [NB100-56498] - Analysis of Somatostatin R5/SSTR5 in human pancreas lysate in the 1) absence and 2) presence of immunizing peptide using Somatostatin Receptor 5 antibody at 0.25 ug/ml.")
![Western Blot: Glut3 Antibody [NBP3-12237] - WB of NBP3-12237 with rat brain. 1:500 antibody dilution in DiluObuffer. Apparent MW is 45-47 kDa.](http://images.novusbio.com/fullsize/Glut3-Antibody-Western-Blot-NBP3-12237-img0002.jpg "Western Blot: Glut3 Antibody [NBP3-12237] - WB of NBP3-12237 with rat brain. 1:500 antibody dilution in DiluObuffer. Apparent MW is 45-47 kDa.")
![Immunohistochemistry-Paraffin: Glut3 Antibody [NBP3-12237] - Rat testis. 1:100 dilution in IHC blocking buffer. DAB (brown) staining and Hematoxylin QS (blue) counterstrain. 40X magnification. FFPE section.](http://images.novusbio.com/fullsize/Glut3-Antibody-Immunohistochemistry-Paraffin-NBP3-12237-img0004.jpg)
![Western Blot: Glut3 Antibody [NBP3-12237] - Cortical extracts (10 ug total protien/lane) on 10% gel. Primary antibody glucose transporter type 3 diluted 1:2000 in Dilobuffer incubation in primary anitbody 120 minutes at RT; washes 3x10 minutes in TBST secondary antibody alkaline phosphatase conjugated goat anti-rabbit IgG (1:5000)](http://images.novusbio.com/fullsize/Glut3-Antibody-Western-Blot-NBP3-12237-img0001.jpg)
![Immunohistochemistry-Paraffin: Glut3 Antibody [NBP3-12237] - Mouse Spleen-NBP3-12237. 1:100 dilution in IHC blocking buffer. DAB (brown) straining and Hematoxylin QS (blue) counterstrain. 40X magnification. FFPE section](http://images.novusbio.com/fullsize/Glut3-Antibody-Immunohistochemistry-Paraffin-NBP3-12237-img0003.jpg)
![Western Blot: Recombinant Human GAPDH Protein [H00002597-P02] - Analysis of GAPDH in GAPDH recombinant protein. Image from verified customer review.](http://images.novusbio.com/fullsize/Recombinant-Human-GAPDH-Protein-Western-Blot-H00002597-P02-img0003.jpg "Western Blot: Recombinant Human GAPDH Protein [H00002597-P02] - Analysis of GAPDH in GAPDH recombinant protein. Image from verified customer review.")
![SDS-Page: Recombinant Human GAPDH Protein [H00002597-P02] - 12.5% SDS-PAGE Stained with Coomassie Blue. Theoretical molecular weight: 62.5 kDa.](http://images.novusbio.com/fullsize/Recombinant-Human-GAPDH-Protein-SDS-Page-H00002597-P02-img0004.jpg)
![Immunocytochemistry/Immunofluorescence: LEDGF Antibody [NBP1-87885] - Staining of human cell line U-2 OS shows localization to nucleoplasm. Antibody staining is shown in green.](http://images.novusbio.com/fullsize/LEDGF-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-87885-img0008.jpg "Immunocytochemistry/Immunofluorescence: LEDGF Antibody [NBP1-87885] - Staining of human cell line U-2 OS shows localization to nucleoplasm. Antibody staining is shown in green.")
