| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26452-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26388-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26182-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26487-50ul | |||
![Western Blot: Nuf2 Antibody (8B7) [NBP3-26452] - Positive Western Blot detected in: Hela whole cell lysate, U251 whole cell lysate. All lanes: Nuf2 Antibody at 1: 2000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 55 kDa Observed band size: 55 kDa](http://images.novusbio.com/fullsize/nbp3-26452_rabbit-nuf2-mab-8b7-28220241141368.jpg "Western Blot: Nuf2 Antibody (8B7) [NBP3-26452] - Positive Western Blot detected in: Hela whole cell lysate, U251 whole cell lysate. All lanes: Nuf2 Antibody at 1: 2000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 55 kDa Observed band size: 55 kDa")
![Western Blot: SMC1 [p Ser957] Antibody (1F9) [NBP3-26388] - Positive Western Blot detected in 293 whole cell lysate (treated with Calyculin A or not). All lanes: SMC1 [p Ser957] Antibody at 1.11ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 160 KDa Observed band size: 160 KDa](http://images.novusbio.com/fullsize/nbp3-26388_rabbit-smc1-p-ser-957-mab-1f9-282202411485814.jpg "Western Blot: SMC1 [p Ser957] Antibody (1F9) [NBP3-26388] - Positive Western Blot detected in 293 whole cell lysate (treated with Calyculin A or not). All lanes: SMC1 [p Ser957] Antibody at 1.11ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 160 KDa Observed band size: 160 KDa")
![Western Blot: Eg5 Antibody (1G11) [NBP3-26182] - Positive Western Blot detected in: MCF-7 whole cell lysate, 293 whole cell lysate, Hela whole cell lysate, U-251 whole cell lysate, K562 whole cell lysate, HepG2 whole cell lysate. All lanes: Eg5 Antibody at 1: 1000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 120 kDa Observed band size: 130 kDa](http://images.novusbio.com/fullsize/nbp3-26182_rabbit-eg5-mab-1g11-28220241140930.jpg "Western Blot: Eg5 Antibody (1G11) [NBP3-26182] - Positive Western Blot detected in: MCF-7 whole cell lysate, 293 whole cell lysate, Hela whole cell lysate, U-251 whole cell lysate, K562 whole cell lysate, HepG2 whole cell lysate. All lanes: Eg5 Antibody at 1: 1000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 120 kDa Observed band size: 130 kDa")
![Immunohistochemistry: E-Cadherin Antibody (1E1) [NBP3-15180] - IHC image of E-Cadherin antibody diluted at 1:100 and staining in paraffin-embedded human breast cancer. 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 30 minutes 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/E-Cadherin-Antibody-1E1-Immunohistochemistry-NBP3-15180-img0001.jpg "Immunohistochemistry: E-Cadherin Antibody (1E1) [NBP3-15180] - IHC image of E-Cadherin antibody diluted at 1:100 and staining in paraffin-embedded human breast cancer. 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 30 minutes 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.")
![Immunocytochemistry/Immunofluorescence: Aurora A Antibody (1H8) [NBP3-26487] - Staining of Hela Cells with Aurora A Antibody (1H8) at 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeated by 0.2% Triton X-100, and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. Nuclear DNA was labeled in blue with DAPI. The secondary antibody was FITC-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26487_rabbit-aurora-a-mab-1h8-282202412493636.jpg "Immunocytochemistry/Immunofluorescence: Aurora A Antibody (1H8) [NBP3-26487] - Staining of Hela Cells with Aurora A Antibody (1H8) at 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeated by 0.2% Triton X-100, and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. Nuclear DNA was labeled in blue with DAPI. The secondary antibody was FITC-conjugated Goat Anti-Rabbit IgG (H+L).")
