| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26484-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26380-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26696-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| IHC-Prediluted | NBP2-48439 | |||
| Azide and BSA Free | NBP3-11496 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-89760-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26212-50ul | |||
![Western Blot: BACE-1 Antibody (7G3) [NBP3-26484] - Positive Western Blot detected in: MCF-7 whole cell lysate, Rat brain tissue, Mouse brain tissue. All lanes: BACE-1 Antibody at 1: 2000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 56, 53, 52, 49, 46, 43 kDa Observed band size: 72 kDa](http://images.novusbio.com/fullsize/nbp3-26484_rabbit-bace-1-mab-7g3-282202411363018.jpg "Western Blot: BACE-1 Antibody (7G3) [NBP3-26484] - Positive Western Blot detected in: MCF-7 whole cell lysate, Rat brain tissue, Mouse brain tissue. All lanes: BACE-1 Antibody at 1: 2000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 56, 53, 52, 49, 46, 43 kDa Observed band size: 72 kDa")
![Immunocytochemistry/Immunofluorescence: PITX3 Antibody (28A9) [NBP3-26380] - Staining of A549 with PITX3 Antibody (28A9) at 1:20, 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 520-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26380_rabbit-pitx3-mab-28a9-28220241312236.jpg "Immunocytochemistry/Immunofluorescence: PITX3 Antibody (28A9) [NBP3-26380] - Staining of A549 with PITX3 Antibody (28A9) at 1:20, 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 520-conjugated Goat Anti-Rabbit IgG (H+L).")
![Flow Cytometry: PITX3 Antibody (28A9) [NBP3-26380] - Overlay Peak curve showing SH-SY5Y cells stained with PITX3 Antibody (28A9) (red line) at 1:50. The cells were fixed in 4% formaldehyde and permeated by 0.2% Triton X-100. Then 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10^6 cells) for 45min at 4C. The secondary antibody used was FITC-conjugated Goat Anti-rabbit IgG (H+L) at 1:200 dilution for 35min at 4C. Control antibody (green line) was rabbit IgG (1ug/1*10^6 cells) used under the same conditions. Acquisition of >10,000 events was performed.](http://images.novusbio.com/fullsize/nbp3-26380_rabbit-pitx3-mab-28a9-282202414183631.jpg)
![Immunocytochemistry/Immunofluorescence: Caspase-9 Antibody (8G5) [NBP3-26696] - Staining of HepG2 with Caspase-9 Antibody (8G5) at 1:7, 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 525-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26696_rabbit-caspase-9-mab-8g5-28220241312232.jpg "Immunocytochemistry/Immunofluorescence: Caspase-9 Antibody (8G5) [NBP3-26696] - Staining of HepG2 with Caspase-9 Antibody (8G5) at 1:7, 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 525-conjugated Goat Anti-Rabbit IgG (H+L).")
![Flow Cytometry: Caspase-9 Antibody (8G5) [NBP3-26696] - Overlay Peak curve showing HepG2 cells stained with Caspase-9 Antibody (8G5) (red line) at 1:50. The cells were fixed in 4% formaldehyde and permeated by 0.2% Triton X-100. Then 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10^6 cells) for 45min at 4C. The secondary antibody used was FITC-conjugated Goat Anti-rabbit IgG (H+L) at 1:200 dilution for 35min at 4C. Control antibody (green line) was rabbit IgG (1ug/1*10^6 cells) used under the same conditions. Acquisition of >10,000 events was performed.](http://images.novusbio.com/fullsize/nbp3-26696_rabbit-caspase-9-mab-8g5-282202414183660.jpg)
![Immunohistochemistry-Paraffin: CD45 Antibody (SPM496) [NBP2-44841] - Human Tonsil stained with CD45 antibody (SPM496) [NBP2-44841].](http://images.novusbio.com/fullsize/CD45-Antibody-SPM496-Immunohistochemistry-Paraffin-NBP2-44841-img0001.jpg "Immunohistochemistry-Paraffin: CD45 Antibody (SPM496) [NBP2-44841] - Human Tonsil stained with CD45 antibody (SPM496) [NBP2-44841].")
![Immunohistochemistry-Paraffin: Glucose Transporter GLUT8 Antibody [NBP1-89760] - Staining of human testis shows strong nuclear and cytoplasmic positivity in cells of seminiferus ducts.](http://images.novusbio.com/fullsize/Glucose-Transporter-GLUT8-Antibody-Immunohistochemistry-Paraffin-NBP1-89760-img0006.jpg "Immunohistochemistry-Paraffin: Glucose Transporter GLUT8 Antibody [NBP1-89760] - Staining of human testis shows strong nuclear and cytoplasmic positivity in cells of seminiferus ducts.")
![Immunohistochemistry: Huntingtin Antibody (6F2) [NBP3-26212] - Image of Huntingtin Antibody (6F2) diluted at 1:100 and staining in paraffin-embedded human small intestine 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 IgG polymer labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26212_rabbit-huntingtin-mab-6f2-262202415355726.jpg "Immunohistochemistry: Huntingtin Antibody (6F2) [NBP3-26212] - Image of Huntingtin Antibody (6F2) diluted at 1:100 and staining in paraffin-embedded human small intestine 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 IgG polymer labeled by HRP and visualized using 0.05% DAB.")
![Immunohistochemistry: Huntingtin Antibody (6F2) [NBP3-26212] - Image of Huntingtin Antibody (6F2) diluted at 1:100 and staining in paraffin-embedded human small intestine 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 IgG polymer labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26212_rabbit-huntingtin-mab-6f2-2722024827494.jpg)