| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26380-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-54324-100ug | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26309-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26116-50ul | |||
![Western Blot: IRS2 Antibody [NB100-68242] - Detection of Human IRS2 NB100-68242. IRS2 was also immunoprecipitated by rabbit anti-IRS2 antibodies NB100-68243 and NB100-68244.](http://images.novusbio.com/fullsize/IRS2-Antibody-Western-Blot-NB100-68242-img0002.jpg "<b>Independent Antibodies Validation. </b>Western Blot: IRS2 Antibody [NB100-68242] - Detection of Human IRS2 NB100-68242. IRS2 was also immunoprecipitated by rabbit anti-IRS2 antibodies NB100-68243 and NB100-68244.")
![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)
![Immunohistochemistry-Paraffin: ACTH Antibody (CLIP/1449) - C-terminus [NBP2-53161] - Formalin-fixed, paraffin-embedded Human Pituitary stained with ACTH Monoclonal Antibody (CLIP/1449).](http://images.novusbio.com/fullsize/ACTH-Antibody-CLIP-1449-C-terminus-Immunohistochemistry-Paraffin-NBP2-53161-img0001.jpg "Immunohistochemistry-Paraffin: ACTH Antibody (CLIP/1449) - C-terminus [NBP2-53161] - Formalin-fixed, paraffin-embedded Human Pituitary stained with ACTH Monoclonal Antibody (CLIP/1449).")
![Western Blot: Noggin Antibody (A5) [NBP3-41971] - Sample: Human Placenta lysate Primary Ab: 1ug/ml NBP3-41971; Second Ab: 0.2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody](http://images.novusbio.com/fullsize/nbp3-41971_mouse-noggin-mab-a5-612202421195686.jpg "Western Blot: Noggin Antibody (A5) [NBP3-41971] - Sample: Human Placenta lysate Primary Ab: 1ug/ml NBP3-41971; Second Ab: 0.2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody")
![Western Blot: Noggin Antibody (A5) [NBP3-41971] - Sample: Human Placenta lysate Primary Ab: 1ug/ml NBP3-41971; Second Ab: 0.2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody](http://images.novusbio.com/fullsize/nbp3-41971_mouse-noggin-mab-a5-61220242195783.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)
![Immunohistochemistry: Ndufs4 Antibody (9H1) [NBP3-26116] - Image of Ndufs4 Antibody (9H1) 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 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26116_rabbit-ndufs4-mab-9h1-27220248573312.jpg "Immunohistochemistry: Ndufs4 Antibody (9H1) [NBP3-26116] - Image of Ndufs4 Antibody (9H1) 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 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB.")
![Flow Cytometry: Ndufs4 Antibody (9H1) [NBP3-26116] - Overlay Peak curve showing MCF7 cells stained with Ndufs4 Antibody (9H1) (red line) at 1:100. 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/nbp3-26116_rabbit-ndufs4-mab-9h1-282202414312761.jpg)