| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26217-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26671-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26695-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26521-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26395-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-33106 | |||
![Immunohistochemistry: HSF1 Antibody (5C7) [NBP3-26217] - Image of HSF1 Antibody (5C7) diluted at 1:100 and staining in paraffin-embedded human ovarian 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/nbp3-26217_rabbit-hsf1-mab-5c7-26220241510618.jpg "Immunohistochemistry: HSF1 Antibody (5C7) [NBP3-26217] - Image of HSF1 Antibody (5C7) diluted at 1:100 and staining in paraffin-embedded human ovarian 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: HSF1 Antibody (5C7) [NBP3-26217] - Image of HSF1 Antibody (5C7) diluted at 1:100 and staining in paraffin-embedded human ovarian 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/nbp3-26217_rabbit-hsf1-mab-5c7-26220241547565.jpg)
![Western Blot: CDC37 Antibody (10C3) [NBP3-26671] - Positive Western Blot detected in: Hela whole cell lysate, Jurkat whole cell lysate, MCF-7 whole cell lysate, 293 whole cell lysate, K562 whole cell lysate, PC-3 whole cell lysate. All lanes: CDC37 Antibody at 1: 2000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 45 kDa Observed band size: 50 kDa](http://images.novusbio.com/fullsize/nbp3-26671_rabbit-cdc37-mab-10c3-28220241152525.jpg "Western Blot: CDC37 Antibody (10C3) [NBP3-26671] - Positive Western Blot detected in: Hela whole cell lysate, Jurkat whole cell lysate, MCF-7 whole cell lysate, 293 whole cell lysate, K562 whole cell lysate, PC-3 whole cell lysate. All lanes: CDC37 Antibody at 1: 2000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 45 kDa Observed band size: 50 kDa")
![Flow Cytometry: CDC37 Antibody (10C3) [NBP3-26671] - Overlay histogram showing Hela cells stained with CDC37 Antibody (10C3) (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/nbp3-26671_rabbit-cdc37-mab-10c3-282202414312749.jpg)
![Western Blot: Caveolin-1 Antibody (2A7) [NBP3-26695] - Positive Western Blot detected in: THP-1 whole cell lysate. All lanes: Caveolin-1 Antibody at 1: 1000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 20 kDa Observed band size: 20 kDa](http://images.novusbio.com/fullsize/nbp3-26695_rabbit-caveolin-1-mab-2a7-28220241140941.jpg "Western Blot: Caveolin-1 Antibody (2A7) [NBP3-26695] - Positive Western Blot detected in: THP-1 whole cell lysate. All lanes: Caveolin-1 Antibody at 1: 1000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 20 kDa Observed band size: 20 kDa")
![Flow Cytometry: Caveolin-1 Antibody (2A7) [NBP3-26695] - Overlay Peak curve showing Hela cells stained with Caveolin-1 Antibody (2A7) (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/nbp3-26695_rabbit-caveolin-1-mab-2a7-282202414312730.jpg)
![Immunohistochemistry: beta-2 Adrenergic R/ADRB2 Antibody (4C11) [NBP3-26521] - Image of beta-2 Adrenergic R/ADRB2 Antibody (4C11) diluted at 1:100 and staining in paraffin-embedded human endometrial 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/nbp3-26521_rabbit-beta-2-adrenergic-r-adrb2-mab-4c11-262202415253325.jpg "Immunohistochemistry: beta-2 Adrenergic R/ADRB2 Antibody (4C11) [NBP3-26521] - Image of beta-2 Adrenergic R/ADRB2 Antibody (4C11) diluted at 1:100 and staining in paraffin-embedded human endometrial 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: beta-2 Adrenergic R/ADRB2 Antibody (4C11) [NBP3-26521] - Image of beta-2 Adrenergic R/ADRB2 Antibody (4C11) diluted at 1:100 and staining in paraffin-embedded human endometrial 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/nbp3-26521_rabbit-beta-2-adrenergic-r-adrb2-mab-4c11-262202415253314.jpg)
![Immunoprecipitation: RSK1 [p Ser380] Antibody (1E11) [NBP3-26395] - Immunoprecipitating RSK1 [p Ser380] Antibody in Hela whole cell lysate. Lane 1: Rabbit control IgG (1ug) instead of NBP3-26395 in Hela whole cell lysate. For western blotting, a HRP-conjugated Protein G antibody was used as the secondary antibody (1/2000). Lane 2: NBP3-26395 (3ug) + Hela whole cell lysate (1mg). Lane 3: Hela whole cell lysate (20ug.)](http://images.novusbio.com/fullsize/nbp3-26395_rabbit-rsk1-p-ser-380-mab-1e11-26220241322153.jpg "Immunoprecipitation: RSK1 [p Ser380] Antibody (1E11) [NBP3-26395] - Immunoprecipitating RSK1 [p Ser380] Antibody in Hela whole cell lysate. Lane 1: Rabbit control IgG (1ug) instead of NBP3-26395 in Hela whole cell lysate. For western blotting, a HRP-conjugated Protein G antibody was used as the secondary antibody (1/2000). Lane 2: NBP3-26395 (3ug) + Hela whole cell lysate (1mg). Lane 3: Hela whole cell lysate (20ug.)")
![Western Blot: RSK1 [p Ser380] Antibody (1E11) [NBP3-26395] - Positive Western Blot detected in A549 whole cell lysate, Hela whole cell lysate, HepG2 whole cell lysate. All lanes: RSK1 [p Ser380] Antibody at 1.75ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 90 KDa Observed band size: 90 KDa](http://images.novusbio.com/fullsize/nbp3-26395_rabbit-rsk1-p-ser-380-mab-1e11-28220241135165.jpg)
![Western Blot: ER alpha/NR3A1 Antibody (ER505) [NBP2-32733] - Western blot analysis of Estrogen Receptor in MCF-7 lysate using Estrogen Receptor Ab (ER505).](http://images.novusbio.com/fullsize/ER-alpha-NR3A1-Antibody-ER505-Western-Blot-NBP2-32733-img0004.jpg "Western Blot: ER alpha/NR3A1 Antibody (ER505) [NBP2-32733] - Western blot analysis of Estrogen Receptor in MCF-7 lysate using Estrogen Receptor Ab (ER505).")
![Western Blot: BID [p Ser78] Antibody [NB500-260] - Detection of Mouse Phospho-BID (S78) after Treatment with EPE. Whole cell lysate (50 and 80 ug for WB; 1 mg for IP, 20% of IP loaded) from NIH3T3 cells that were treated with etoposide (100 mcM; 3 hours) or mock treated. Antibody used at 1 ug/ml.](http://images.novusbio.com/fullsize/BID-[p-Ser78]-Antibody-Western-Blot-NB500-260-img0004.jpg "Western Blot: BID [p Ser78] Antibody [NB500-260] - Detection of Mouse Phospho-BID (S78) after Treatment with EPE. Whole cell lysate (50 and 80 ug for WB; 1 mg for IP, 20% of IP loaded) from NIH3T3 cells that were treated with etoposide (100 mcM; 3 hours) or mock treated. Antibody used at 1 ug/ml.")
![Western Blot: BRCA1 [p Ser1280] Antibody [NB100-224] - Detection of Brca1 phospho Ser 1280 by Western Blot using Rabbit anti-Brca1 pSer1280 (cat. no. NB100-224).](http://images.novusbio.com/fullsize/BRCA1-[p-Ser1280]-Antibody-Western-Blot-NB100-224-img0001.jpg "Western Blot: BRCA1 [p Ser1280] Antibody [NB100-224] - Detection of Brca1 phospho Ser 1280 by Western Blot using Rabbit anti-Brca1 pSer1280 (cat. no. NB100-224).")
![Immunoprecipitation: ABI1 Antibody [NB100-59843] - Detection of Human ABI1 on HeLa whole cell lysate using NB100-59843. ABI1 was also immunoprecipitated by rabbit anti-ABI1 antibodies NB100-59844 and NB100-59845.](http://images.novusbio.com/fullsize/ABI1-Antibody-Immunoprecipitation-NB100-59843-img0002.jpg "Immunoprecipitation: ABI1 Antibody [NB100-59843] - Detection of Human ABI1 on HeLa whole cell lysate using NB100-59843. ABI1 was also immunoprecipitated by rabbit anti-ABI1 antibodies NB100-59844 and NB100-59845.")
![Western Blot: BRCA1 [p Ser1189] Antibody [NB100-229] - Detection of Brca1 Phosph Ser 1189 by Western Blot using Rabbit anti-BRCA1 [p Ser1189] Antibody.](http://images.novusbio.com/fullsize/BRCA1-[p-Ser1189]-Antibody-Western-Blot-NB100-229-img0001.jpg "Western Blot: BRCA1 [p Ser1189] Antibody [NB100-229] - Detection of Brca1 Phosph Ser 1189 by Western Blot using Rabbit anti-BRCA1 [p Ser1189] Antibody.")
![Western Blot: BRCA1 [p Ser1466] Antibody [NB100-228] - Whole Cell Lysate (25ug/lane) from Hela cells treated with 10 Gy IR or untreated. Antibody diluted 1:2000](http://images.novusbio.com/fullsize/BRCA1-[p-Ser1466]-Antibody-Western-Blot-NB100-228-img0002.jpg "<b>Biological Strategies Validation. </b>Western Blot: BRCA1 [p Ser1466] Antibody [NB100-228] - Whole Cell Lysate (25ug/lane) from Hela cells treated with 10 Gy IR or untreated. Antibody diluted 1:2000")
![Western Blot: ASAP1 Antibody [NBP1-19159] - ASAP1 by Western Blot and Immunoprecipitation: [NBP1-19159]- Whole cell lysate (5, 15 and 50 ug for WB; 1 mg for IP, 20% of IP loaded) from HeLa cells used for WB at 0.04 ug/ml (A) and 1 ug/ml (B) and used for IP at 3 ug/mg lysate. ASAP1 was also immunoprecipitated by rabbit anti-ASAP1 antibody NBP1-19158, which recognizes an upstream epitope.](http://images.novusbio.com/fullsize/ASAP1-Antibody-Western-Blot-NBP1-19159-img0002.jpg "<b>Independent Antibodies Validation. </b>Western Blot: ASAP1 Antibody [NBP1-19159] - ASAP1 by Western Blot and Immunoprecipitation: [NBP1-19159]- Whole cell lysate (5, 15 and 50 ug for WB; 1 mg for IP, 20% of IP loaded) from HeLa cells used for WB at 0.04 ug/ml (A) and 1 ug/ml (B) and used for IP at 3 ug/mg lysate. ASAP1 was also immunoprecipitated by rabbit anti-ASAP1 antibody NBP1-19158, which recognizes an upstream epitope.")