| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26487-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-29791-0.025ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26372-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26429-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26146-50ul | |||
![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).")
![Immunoprecipitation: CENPE Antibody [NBP1-06506] - Whole cell lysate (1 mg for IP, 20% of IP loaded) from HeLa cells. Antibodies: Affinity purified rabbit anti-CENP-E antibody NBP1-06506used for IP at 3 ug/mg lysate. CENP-E was also immunoprecipitated by rabbit anti-CENP-E antibodies NBP1-06504 and NBP1-06505, which recognize upstream epitopes.](http://images.novusbio.com/fullsize/CENPE-Antibody-Immunoprecipitation-NBP1-06506-img0004.jpg "<b>Independent Antibodies Validation. </b>Immunoprecipitation: CENPE Antibody [NBP1-06506] - Whole cell lysate (1 mg for IP, 20% of IP loaded) from HeLa cells. Antibodies: Affinity purified rabbit anti-CENP-E antibody NBP1-06506used for IP at 3 ug/mg lysate. CENP-E was also immunoprecipitated by rabbit anti-CENP-E antibodies NBP1-06504 and NBP1-06505, which recognize upstream epitopes.")
![Western Blot: Cyclophilin A Antibody (4G3) [NBP3-26372] - Positive Western Blot detected in: Raji whole cell lysate, HepG2 whole cell lysate. All lanes: Cyclophilin A Antibody at 1: 1500 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 19, 12 kDa Observed band size: 19 kDa](http://images.novusbio.com/fullsize/nbp3-26372_rabbit-cyclophilin-a-mab-4g3-28220241140939.jpg "Western Blot: Cyclophilin A Antibody (4G3) [NBP3-26372] - Positive Western Blot detected in: Raji whole cell lysate, HepG2 whole cell lysate. All lanes: Cyclophilin A Antibody at 1: 1500 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 19, 12 kDa Observed band size: 19 kDa")
![Immunoprecipitation: DLG5 Antibody [NBP1-28694] - Samples: Whole cell lysate (1 mg for IP, 20% of IP loaded) from HeLa cells. Antibodies: Affinity purified rabbit anti-DLG5 antibody NBP1-28694 used for IP at 10 ug/mg lysate. DLG5 was also immunoprecipitated by rabbit anti-DLG5 antibody NBP1-28739, which recognizes a downstream epitope. For blotting immunoprecipitated DLG5, NBP1-28739 was used at 1 ug/ml. Detection: Chemiluminescence with an exposure time of 30 seconds.](http://images.novusbio.com/fullsize/DLG5-Antibody-Immunoprecipitation-NBP1-28694-img0001.jpg "Immunoprecipitation: DLG5 Antibody [NBP1-28694] - Samples: Whole cell lysate (1 mg for IP, 20% of IP loaded) from HeLa cells. Antibodies: Affinity purified rabbit anti-DLG5 antibody NBP1-28694 used for IP at 10 ug/mg lysate. DLG5 was also immunoprecipitated by rabbit anti-DLG5 antibody NBP1-28739, which recognizes a downstream epitope. For blotting immunoprecipitated DLG5, NBP1-28739 was used at 1 ug/ml. Detection: Chemiluminescence with an exposure time of 30 seconds.")
![Western Blot: CDC37 [p Ser13] Antibody (3B3) [NBP3-26429] - Positive Western Blot detected in Hela whole cell lysate. All lanes: CDC37 [p Ser13] Antibody at 0.6ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 50 KDa Observed band size: 50 KDa](http://images.novusbio.com/fullsize/nbp3-26429_rabbit-cdc37-p-ser-13-mab-3b3-282202411485844.jpg "Western Blot: CDC37 [p Ser13] Antibody (3B3) [NBP3-26429] - Positive Western Blot detected in Hela whole cell lysate. All lanes: CDC37 [p Ser13] Antibody at 0.6ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 50 KDa Observed band size: 50 KDa")
![Immunohistochemistry-Paraffin: MUC5B Antibody (C1) [NBP3-41205] - DAB staining on IHC-P; Sample: Human Small intestine Tissue; Primary Ab: 30ug/ml NBP3-41205; Second Ab: 2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody](http://images.novusbio.com/fullsize/nbp3-41205_mouse-muc5b-mab-c1-61220242128385.jpg "Immunohistochemistry-Paraffin: MUC5B Antibody (C1) [NBP3-41205] - DAB staining on IHC-P; Sample: Human Small intestine Tissue; Primary Ab: 30ug/ml NBP3-41205; Second Ab: 2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody")
![Western Blot: TGF-beta 2 Antibody (F9) [NBP3-41204] - Sample: Lane1: K562 cell lysate; Lane2: U2OS cell lysate Primary Ab: 0.05ug/ml NBP3-41204; Second Ab: 0.2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody](http://images.novusbio.com/fullsize/nbp3-41204_mouse-tgf-beta-2-mab-f9-612202421304314.jpg "Western Blot: TGF-beta 2 Antibody (F9) [NBP3-41204] - Sample: Lane1: K562 cell lysate; Lane2: U2OS cell lysate Primary Ab: 0.05ug/ml NBP3-41204; Second Ab: 0.2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody")
![Western Blot: MUC5B Antibody (D7) [NBP3-41189] - Sample: Human Saliva Primary Ab: 1ug/ml NBP3-41189; Second Ab: 0.2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody](http://images.novusbio.com/fullsize/nbp3-41189_mouse-muc5b-mab-d7-612202421283883.jpg "Western Blot: MUC5B Antibody (D7) [NBP3-41189] - Sample: Human Saliva Primary Ab: 1ug/ml NBP3-41189; Second Ab: 0.2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody")
![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.")
![Immunohistochemistry: Midkine Antibody (2G3) [NBP3-26146] - Image of Midkine Antibody (2G3) diluted at 1:100 and staining in paraffin-embedded human pancreatic 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/nbp3-26146_rabbit-midkine-mab-2g3-262202415475631.jpg "Immunohistochemistry: Midkine Antibody (2G3) [NBP3-26146] - Image of Midkine Antibody (2G3) diluted at 1:100 and staining in paraffin-embedded human pancreatic 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.")