| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-97160-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-99642-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-00186-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-89254-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-90470-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-98355-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-99490-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-99716-50ul | |||
![Western Blot: Nudel Antibody [NBP2-97160] - Anti-Nudel rabbit polyclonal antibody at 1:500 dilution. Lane A: HeLa Whole Cell Lysate Lane B: Jurkat Whole Cell Lysate Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG (H+L)/HRP at 1/10000 dilution. Developed using the ECL technique. Performed under reducing conditions. Predicted band size: 38 kDa. Observed band size: 43 kDa](http://images.novusbio.com/fullsize/Nudel-Antibody-Western-Blot-NBP2-97160-img0003.jpg "Western Blot: Nudel Antibody [NBP2-97160] - Anti-Nudel rabbit polyclonal antibody at 1:500 dilution. Lane A: HeLa Whole Cell Lysate Lane B: Jurkat Whole Cell Lysate Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG (H+L)/HRP at 1/10000 dilution. Developed using the ECL technique. Performed under reducing conditions. Predicted band size: 38 kDa. Observed band size: 43 kDa")
![Immunoprecipitation: Nudel Antibody [NBP2-97160] - Nudel was immunoprecipitated using: Lane A: 0.5 mg HeLa Whole Cell Lysate 4 ul anti-Nudel rabbit polyclonal antibody and 60 ug of Immunomagnetic beads Protein A/G. Primary antibody: Anti-Nudel rabbit polyclonal antibody, at 1:100 dilution. Secondary antibody: Goat Anti-Rabbit IgG (H+L)/HRP at 1/10000 dilution. Developed using the ECL technique. Performed under reducing conditions. Predicted band size: 38 kDa. Observed band size: 43 kDa.](http://images.novusbio.com/fullsize/Nudel-Antibody-Immunoprecipitation-NBP2-97160-img0004.jpg)
![Western Blot: 14-3-3 eta Antibody [NBP2-99642] - Anti-14-3-3 eta rabbit polyclonal antibody at 1:500 dilution. Lane A: U937 Whole Cell Lysate. Lane B: 293T Whole Cell Lysate. Lane C: Jurkat Whole Cell Lysate. Lane D: K562 Whole Cell Lysate. Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG H&L (Dylight 800) at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size: 33 kDa. Observed band size: 31 kDa](http://images.novusbio.com/fullsize/14-3-3-eta-Antibody-Western-Blot-NBP2-99642-img0003.jpg "Western Blot: 14-3-3 eta Antibody [NBP2-99642] - Anti-14-3-3 eta rabbit polyclonal antibody at 1:500 dilution. Lane A: U937 Whole Cell Lysate. Lane B: 293T Whole Cell Lysate. Lane C: Jurkat Whole Cell Lysate. Lane D: K562 Whole Cell Lysate. Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG H&L (Dylight 800) at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size: 33 kDa. Observed band size: 31 kDa")
![Immunoprecipitation: 14-3-3 eta Antibody [NBP2-99642] - 14-3-3 eta was immunoprecipitated using: Lane A: 0.5 mg 293T Whole Cell Lysate. Lane B: 0.5 mg Jurkat Whole Cell Lysate. Lane C: 0.5 mg k562 Whole Cell Lysate. Lane D:0.5 mg NIH-3T3 Whole Cell Lysate. 2 ul anti-14-3-3 eta rabbit polyclonal antibody and 15 ul of 50 % Protein G agarose. Primary antibody: Anti-14-3-3 eta rabbit polyclonal antibody, at 1:2000 dilution. Secondary antibody: Dylight 800-labeled antibody to rabbit IgG (H+L), at 1:5000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size: 28 kDa. Observed band size: 28 kDa](http://images.novusbio.com/fullsize/14-3-3-eta-Antibody-Immunoprecipitation-NBP2-99642-img0004.jpg)
![Immunohistochemistry-Paraffin: Glutaminyl-peptide Cyclotransferase/Glutaminyl-peptide Cyclotransferase/QPCT Antibody [NBP3-00186] - Immunochemical staining of human Glutaminyl-peptide Cyclotransferase/QPCT in human thyroid with NBP3-00186 (1:2000, formalin-fixed paraffin embedded sections).](http://images.novusbio.com/fullsize/nbp3-00186_rabbit-polyclonal-glutaminyl-peptide-cyclotransferase-qpct-antibody-23520251129359.png "Immunohistochemistry-Paraffin: Glutaminyl-peptide Cyclotransferase/Glutaminyl-peptide Cyclotransferase/QPCT Antibody [NBP3-00186] - Immunochemical staining of human Glutaminyl-peptide Cyclotransferase/QPCT in human thyroid with NBP3-00186 (1:2000, formalin-fixed paraffin embedded sections).")
![Immunohistochemistry-Paraffin: Glutaminyl-peptide Cyclotransferase/Glutaminyl-peptide Cyclotransferase/QPCT Antibody [NBP3-00186] - Immunochemical staining of human Glutaminyl-peptide Cyclotransferase/QPCT in human brain with NBP3-00186 (1:2000, formalin-fixed paraffin embedded sections).](http://images.novusbio.com/fullsize/nbp3-00186_rabbit-polyclonal-glutaminyl-peptide-cyclotransferase-qpct-antibody-23520251129358.png)
![Immunocytochemistry/Immunofluorescence: BACE-1 Antibody (027) [NBP2-89254] - Staining of Human BACE1 in Hela cells. Cells were fixed with 4% PFA, permeabilzed with 1% Triton X-100 in PBS, blocked with 10% serum, and incubated with rabbit anti-Human AK4 monoclonal antibody (1:60) at 37c 1 hour. Then cells were stained with the Alexa Fluor(R)488-conjugated Goat Anti-rabbit IgG secondary antibody (green) and counterstained with DAPI (blue). Positive staining was localized to cytoplasm.](http://images.novusbio.com/fullsize/BACE-1-Antibody-027-Immunocytochemistry-Immunofluorescence-NBP2-89254-img0001.jpg "Immunocytochemistry/Immunofluorescence: BACE-1 Antibody (027) [NBP2-89254] - Staining of Human BACE1 in Hela cells. Cells were fixed with 4% PFA, permeabilzed with 1% Triton X-100 in PBS, blocked with 10% serum, and incubated with rabbit anti-Human AK4 monoclonal antibody (1:60) at 37c 1 hour. Then cells were stained with the Alexa Fluor(R)488-conjugated Goat Anti-rabbit IgG secondary antibody (green) and counterstained with DAPI (blue). Positive staining was localized to cytoplasm.")
![Flow Cytometry: BACE-1 Antibody (027) [NBP2-89254] - Analysis of Human BACE1 expression on Jurkat cells. The cells were treated stained with purified anti-Human BACE1, then a FITC-conjugated second step antibody. The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of intact cells.](http://images.novusbio.com/fullsize/BACE-1-Antibody-027-Flow-Cytometry-NBP2-89254-img0002.jpg)
![Immunohistochemistry-Paraffin: CD38 Antibody (32) [NBP2-90470] - Staining of mouse CD38 in mouse kidney with rabbit monoclonal antibody (1:500, formalin-fixed paraffin embedded sections). Positive staining was localized to endotheliocyte.](http://images.novusbio.com/fullsize/CD38-Antibody-32-Immunohistochemistry-Paraffin-NBP2-90470-img0002.jpg "Immunohistochemistry-Paraffin: CD38 Antibody (32) [NBP2-90470] - Staining of mouse CD38 in mouse kidney with rabbit monoclonal antibody (1:500, formalin-fixed paraffin embedded sections). Positive staining was localized to endotheliocyte.")
![Immunohistochemistry-Paraffin: CD38 Antibody (32) [NBP2-90470] - Staining of mouse CD38 in mouse heart with rabbit monoclonal antibody (1:500, formalin-fixed paraffin embedded sections). Positive staining was localized to endotheliocyte.](http://images.novusbio.com/fullsize/CD38-Antibody-32-Immunohistochemistry-Paraffin-NBP2-90470-img0001.jpg)
![Western Blot: Thimet Oligopeptidase/THOP1 Antibody [NBP2-98355] - Anti-Thimet Oligopeptidase/THOP1 rabbit polyclonal antibody at 1:500 dilution. Lane A: HCT116 Whole Cell Lysate. Lane B: HELA Whole Cell Lysate. Lane C: K562 Whole Cell Lysate. Lane D: 293T Whole Cell Lysate. Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG H&L (Dylight 800) at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size: 79 kDa. Observed band size: 72 kDa](http://images.novusbio.com/fullsize/Thimet-Oligopeptidase-THOP1-Antibody-Western-Blot-NBP2-98355-img0003.jpg "Western Blot: Thimet Oligopeptidase/THOP1 Antibody [NBP2-98355] - Anti-Thimet Oligopeptidase/THOP1 rabbit polyclonal antibody at 1:500 dilution. Lane A: HCT116 Whole Cell Lysate. Lane B: HELA Whole Cell Lysate. Lane C: K562 Whole Cell Lysate. Lane D: 293T Whole Cell Lysate. Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG H&L (Dylight 800) at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size: 79 kDa. Observed band size: 72 kDa")
![Immunoprecipitation: Thimet Oligopeptidase/THOP1 Antibody [NBP2-98355] - Mouse Thimet Oligopeptidase/THOP1 was immunoprecipitated using: Lane A: 0.5 mg K562 Whole Cell Lysate 2 ul anti-Mouse Thimet Oligopeptidase/THOP1 rabbit polyclonal antibody and 15 ul of 50 % Protein G agarose. Primary antibody: Anti-Mouse Thimet Oligopeptidase/THOP1 rabbit polyclonal antibody, at 1:200 dilution. Secondary antibody: Dylight 800-labeled antibody to rabbit IgG (H+L), at 1:5000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size: 80 kDa. Observed band size: 80 kDa](http://images.novusbio.com/fullsize/Thimet-Oligopeptidase-THOP1-Antibody-Immunoprecipitation-NBP2-98355-img0004.jpg)
![Western Blot: 14-3-3 eta Antibody [NBP2-99490] - Anti-14-3-3 eta rabbit polyclonal antibody at 1:500 dilution. Lane A: Jurkat Whole Cell Lysate. Lane B: A375 Whole Cell Lysate. Lane C: 293T Whole Cell Lysate. Lane D: K562 Whole Cell Lysate. Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG (H+L)/HRP at 1/10000 dilution. Developed using the ECL technique. Performed under reducing conditions. Predicted band size: 28 kDa. Observed band size: 28 kDax](http://images.novusbio.com/fullsize/14-3-3-eta-Antibody-Western-Blot-NBP2-99490-img0003.jpg "Western Blot: 14-3-3 eta Antibody [NBP2-99490] - Anti-14-3-3 eta rabbit polyclonal antibody at 1:500 dilution. Lane A: Jurkat Whole Cell Lysate. Lane B: A375 Whole Cell Lysate. Lane C: 293T Whole Cell Lysate. Lane D: K562 Whole Cell Lysate. Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG (H+L)/HRP at 1/10000 dilution. Developed using the ECL technique. Performed under reducing conditions. Predicted band size: 28 kDa. Observed band size: 28 kDax")
![Immunoprecipitation: 14-3-3 eta Antibody [NBP2-99490] - Lane A:0.5 mg A375 Whole Cell Lysate4 uL anti-YWHAH rabbit polyclonal antibody and 60 ug of Immunomagnetic beads Protein A/G.Primary antibody:Anti-YWHAH rabbit polyclonal antibody,at 1:100 dilutionSecondary antibody:Goat Anti-Rabbit IgG (H+L)/HRP at 1/10000 dilutionDeveloped using the ECL technique.Performed under reducing conditions.Predicted band size: 28 kDaObserved band size :28 kDa](http://images.novusbio.com/fullsize/antibody/nbp2-99490_rabbit-polyclonal-14-3-3-eta-antibody-immunoprecipitation-287202374410.jpg)
![Immunohistochemistry-Paraffin: S100A3 Antibody [NBP2-99716] - Immunochemical staining of human S100A3 in human tonsil with rabbit polyclonal antibody (1:1000, formalin-fixed paraffin embedded sections). The image showing positive staining in tonsil crypt.](http://images.novusbio.com/fullsize/S100A3-Antibody-Immunohistochemistry-Paraffin-NBP2-99716-img0002.jpg "Immunohistochemistry-Paraffin: S100A3 Antibody [NBP2-99716] - Immunochemical staining of human S100A3 in human tonsil with rabbit polyclonal antibody (1:1000, formalin-fixed paraffin embedded sections). The image showing positive staining in tonsil crypt.")
![Immunohistochemistry-Paraffin: S100A3 Antibody [NBP2-99716] - Immunochemical staining of human S100A3 in human tonsil with rabbit polyclonal antibody (1:1000, formalin-fixed paraffin embedded sections). The image showing positive staining in tonsil crypt.](http://images.novusbio.com/fullsize/S100A3-Antibody-Immunohistochemistry-Paraffin-NBP2-99716-img0001.jpg)
![Immunohistochemistry: Substance P Antibody (JE59-73) [NBP3-32984] - Immunohistochemical analysis of paraffin-embedded rat spinal cord tissue with Rabbit anti-Substance P antibody (NBP3-32984) 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 (NBP3-32984) 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/nbp3-32984_rabbit-substance-p-mab-je59-73-298202414115438.jpg "Immunohistochemistry: Substance P Antibody (JE59-73) [NBP3-32984] - Immunohistochemical analysis of paraffin-embedded rat spinal cord tissue with Rabbit anti-Substance P antibody (NBP3-32984) 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 (NBP3-32984) 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.")
![Immunohistochemistry: Enolase 2/Neuron-specific Enolase Antibody (NSE-P2) [NBP3-30895] - Left and Center: Immunohistochemical staining of normal pancreas tissue (left) and small bowel tumor tissue (center) using NSE antibody (X2070M and NBP3-30895).Right: Western blot analysis using NSE antibodies (X2070M and NBP3-30895) on alpha and gamma enolase standards.](http://images.novusbio.com/fullsize/nbp3-30895_mouse-enolase-2-neuron-specific-enolase-mab-nse-p2-811202420594228.jpg "Immunohistochemistry: Enolase 2/Neuron-specific Enolase Antibody (NSE-P2) [NBP3-30895] - Left and Center: Immunohistochemical staining of normal pancreas tissue (left) and small bowel tumor tissue (center) using NSE antibody (X2070M and NBP3-30895).Right: Western blot analysis using NSE antibodies (X2070M and NBP3-30895) on alpha and gamma enolase standards.")
![Western Blot: Tau [p Ser202] Antibody (JE66-81) [NBP3-32804] - Western blot analysis of Tau on different lysates with Rabbit anti-Tau antibody (NBP3-32804) at 1/2,000 dilution. Lane 1: Mouse brain tissue lysate Lane 2: Rat hippocampus tissue lysate Lane 3: Mouse brain treated with pp for 1 hour tissue lysate Lysates/proteins at 30 ug/Lane. Predicted band size: 79 kDa Observed band size: 45-70 kDa Exposure time: 1 minute 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 (NBP3-32804) 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/nbp3-32804_rabbit-tau-p-ser202-mab-je66-81-288202412442917.jpg "Western Blot: Tau [p Ser202] Antibody (JE66-81) [NBP3-32804] - Western blot analysis of Tau on different lysates with Rabbit anti-Tau antibody (NBP3-32804) at 1/2,000 dilution. Lane 1: Mouse brain tissue lysate Lane 2: Rat hippocampus tissue lysate Lane 3: Mouse brain treated with pp for 1 hour tissue lysate Lysates/proteins at 30 ug/Lane. Predicted band size: 79 kDa Observed band size: 45-70 kDa Exposure time: 1 minute 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 (NBP3-32804) 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.")
![Western Blot: Tau [p Ser214] Antibody (JE66-83) [NBP3-32805] - Western blot analysis of Tau on different lysates with Rabbit anti-Tau antibody (NBP3-32805) at 1/1,000 dilution. Lane 1: SH-SY5Y cell lysate Lane 2: SH-SY5Y treated with 200nM Calyculin A and 1uM Okadaic Acid for 1 hour cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 79 kDa Observed band size: 40-55 kDa Exposure time: 5 minutes; 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 (NBP3-32805) at 1/1,000 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/nbp3-32805_rabbit-tau-p-ser214-mab-je66-83-288202412442910.jpg "Western Blot: Tau [p Ser214] Antibody (JE66-83) [NBP3-32805] - Western blot analysis of Tau on different lysates with Rabbit anti-Tau antibody (NBP3-32805) at 1/1,000 dilution. Lane 1: SH-SY5Y cell lysate Lane 2: SH-SY5Y treated with 200nM Calyculin A and 1uM Okadaic Acid for 1 hour cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 79 kDa Observed band size: 40-55 kDa Exposure time: 5 minutes; 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 (NBP3-32805) at 1/1,000 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.")