| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26114-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-81571-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26603-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26309-50ul | |||
![Immunocytochemistry/Immunofluorescence: NeuroD1 Antibody (5D2) [NBP3-26114] - Staining of A549 with NeuroD1 Antibody (5D2) at 1:60, 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 522-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26114_rabbit-neurod1-mab-5d2-28220241312219.jpg "Immunocytochemistry/Immunofluorescence: NeuroD1 Antibody (5D2) [NBP3-26114] - Staining of A549 with NeuroD1 Antibody (5D2) at 1:60, 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 522-conjugated Goat Anti-Rabbit IgG (H+L).")
![Flow Cytometry: NeuroD1 Antibody (5D2) [NBP3-26114] - Overlay Peak curve showing SH-SY5Y cells stained with NeuroD1 Antibody (5D2) (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/nbp3-26114_rabbit-neurod1-mab-5d2-28220241418368.jpg)
![Immunohistochemistry-Paraffin: KCNK10 Antibody [NBP1-81571] - Staining of human pancreas shows strong cytoplasmic positivity in exocrine glandular cells.](http://images.novusbio.com/fullsize/KCNK10-Antibody-Immunohistochemistry-Paraffin-NBP1-81571-img0002.jpg "Immunohistochemistry-Paraffin: KCNK10 Antibody [NBP1-81571] - Staining of human pancreas shows strong cytoplasmic positivity in exocrine glandular cells.")
![Immunohistochemistry: Neutrophil Elastase/ELA2 Antibody (2H12) [NBP3-26603] - Image of Neutrophil Elastase/ELA2 Antibody (2H12) diluted at 1:100 and staining in paraffin-embedded human spleen 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/nbp3-26603_rabbit-neutrophil-elastase-ela2-mab-2h12-272202485634.jpg "Immunohistochemistry: Neutrophil Elastase/ELA2 Antibody (2H12) [NBP3-26603] - Image of Neutrophil Elastase/ELA2 Antibody (2H12) diluted at 1:100 and staining in paraffin-embedded human spleen 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.")
![Flow Cytometry: Neutrophil Elastase/ELA2 Antibody (2H12) [NBP3-26603] - Overlay histogram showing Jurkat cells stained with Neutrophil Elastase/ELA2 Antibody (2H12) (red line) at 1:50. The cells were fixed with 70% Ethylalcohol (18h) and then incubated in 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10^6 cells) for 1 h at 4C. The secondary antibody used was FITC-conjugated goat anti-rabbit IgG (H+L) at 1/200 dilution for 30min 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/nbp3-26603_rabbit-neutrophil-elastase-ela2-mab-2h12-282202414183686.jpg)
![Western Blot: SOD1/Cu-Zn SOD Antibody (3E5) [NBP3-26309] - Positive Western Blot detected in: 293 whole cell lysate, Hela whole cell lysate, Jurkat whole cell lysate, MCF-7 whole cell lysate, K562 whole cell lysate, HepG2 whole cell lysate, U87 whole cell lysate. All lanes: SOD1/Cu-Zn SOD Antibody at 1: 1500 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 16 kDa Observed band size: 18 kDa](http://images.novusbio.com/fullsize/nbp3-26309_rabbit-sod1-cu-zn-sod-mab-3e5-282202411472130.jpg "Western Blot: SOD1/Cu-Zn SOD Antibody (3E5) [NBP3-26309] - Positive Western Blot detected in: 293 whole cell lysate, Hela whole cell lysate, Jurkat whole cell lysate, MCF-7 whole cell lysate, K562 whole cell lysate, HepG2 whole cell lysate, U87 whole cell lysate. All lanes: SOD1/Cu-Zn SOD Antibody at 1: 1500 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 16 kDa Observed band size: 18 kDa")
![Flow Cytometry: SOD1/Cu-Zn SOD Antibody (3E5) [NBP3-26309] - Overlay histogram showing Jurkat cells stained with SOD1/Cu-Zn SOD Antibody (3E5) (red line) at 1:50. The cells were fixed with 70% Ethylalcohol (18h) and then incubated in 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10^6 cells) for 1 h at 4C. The secondary antibody used was FITC-conjugated goat anti-rabbit IgG (H+L) at 1/200 dilution for 30min 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/nbp3-26309_rabbit-sod1-cu-zn-sod-mab-3e5-282202414183676.jpg)