| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26393-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26487-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26580-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26582-50ul | |||
![Immunohistochemistry: MSK1/RPS6KA5 [p Ser376] Antibody (2F3) [NBP3-26393] - Image of MSK1/RPS6KA5 [p Ser376] Antibody (2F3) diluted at 1:100 and staining in paraffin-embedded human bladder cancer 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 biotinylated secondary antibody and visualized using an HRP conjugated SP system.](http://images.novusbio.com/fullsize/nbp3-26393_rabbit-msk1-rps6ka5-p-ser-376-mab-2f3-262202414471568.jpg "Immunohistochemistry: MSK1/RPS6KA5 [p Ser376] Antibody (2F3) [NBP3-26393] - Image of MSK1/RPS6KA5 [p Ser376] Antibody (2F3) diluted at 1:100 and staining in paraffin-embedded human bladder cancer 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 biotinylated secondary antibody and visualized using an HRP conjugated SP system.")
![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).")
![Western Blot: Bub1 Antibody (9C11) [NBP3-15170] - Positive WB detected in: Hela whole cell lysate, K562 whole cell lysate, HepG2 whole cell lysate. All lanes: Bub1 antibody at 1:1000. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 123, 116, 120 KDa. Observed band size: 130 KDa.](http://images.novusbio.com/fullsize/Bub1-Antibody-9C11-Western-Blot-NBP3-15170-img0001.jpg "Western Blot: Bub1 Antibody (9C11) [NBP3-15170] - Positive WB detected in: Hela whole cell lysate, K562 whole cell lysate, HepG2 whole cell lysate. All lanes: Bub1 antibody at 1:1000. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 123, 116, 120 KDa. Observed band size: 130 KDa.")
![Immunohistochemistry: FGFR4 Antibody (8A5) [NBP3-26580] - Image of FGFR4 Antibody (8A5) diluted at 1:100 and staining in paraffin-embedded human breast cancer 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/nbp3-26580_rabbit-fgfr4-mab-8a5-262202415355727.jpg "Immunohistochemistry: FGFR4 Antibody (8A5) [NBP3-26580] - Image of FGFR4 Antibody (8A5) diluted at 1:100 and staining in paraffin-embedded human breast cancer 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: LRRK2 Antibody (4E9) [NBP3-15156] - IHC image of LRRK2 antibody diluted at 1:100 and staining in paraffin-embedded human kidney tissue. 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/LRRK2-Antibody-4E9-Immunohistochemistry-NBP3-15156-img0001.jpg "Immunohistochemistry: LRRK2 Antibody (4E9) [NBP3-15156] - IHC image of LRRK2 antibody diluted at 1:100 and staining in paraffin-embedded human kidney tissue. 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.")
![Western Blot: FGFR3 Antibody (6D4) [NBP3-26582] - Positive Western Blot detected in: U87 whole cell lysate, 293 whole cell lysate, Hela whole cell lysate. All lanes: FGFR3 Antibody at 1: 2000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 88, 89, 76, 86 kDa Observed band size: 115 kDa](http://images.novusbio.com/fullsize/nbp3-26582_rabbit-fgfr3-mab-6d4-28220241147214.jpg "Western Blot: FGFR3 Antibody (6D4) [NBP3-26582] - Positive Western Blot detected in: U87 whole cell lysate, 293 whole cell lysate, Hela whole cell lysate. All lanes: FGFR3 Antibody at 1: 2000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 88, 89, 76, 86 kDa Observed band size: 115 kDa")