| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-47775-0.1mg | |||
| IHC-Prediluted | NBP2-48272 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-54429-100ug | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26159-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26606-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-56485-25ul | |||
![Immunohistochemistry-Paraffin: ZAP70 Antibody (ZAP70/528 + 2F3.2) [NBP2-44505] - Human Tonsil stained with ZAP70 Monoclonal Antibody (ZAP70/528 + 2F3.2).](http://images.novusbio.com/fullsize/ZAP70-Antibody-ZAP70-528-+-2F3-2-Immunohistochemistry-Paraffin-NBP2-44505-img0001.jpg "Immunohistochemistry-Paraffin: ZAP70 Antibody (ZAP70/528 + 2F3.2) [NBP2-44505] - Human Tonsil stained with ZAP70 Monoclonal Antibody (ZAP70/528 + 2F3.2).")
![Immunohistochemistry-Paraffin: CEACAM5/CD66e Antibody (C66/1291) [NBP2-53350] - Human Colon stained with CEACAM5/CD66e Antibody (C66/1291).](http://images.novusbio.com/fullsize/CEACAM5-CD66e-Antibody-C66-1291-Immunohistochemistry-Paraffin-NBP2-53350-img0002.jpg "Immunohistochemistry-Paraffin: CEACAM5/CD66e Antibody (C66/1291) [NBP2-53350] - Human Colon stained with CEACAM5/CD66e Antibody (C66/1291).")
![Immunohistochemistry-Paraffin: CEACAM5/CD66e Antibody (C66/1291) [NBP2-53350] - Human Colon stained with CEACAM5/CD66e Antibody (C66/1291).](http://images.novusbio.com/fullsize/CEACAM5-CD66e-Antibody-C66-1291-Immunohistochemistry-Paraffin-NBP2-53350-img0001.jpg)
![Immunocytochemistry/Immunofluorescence: LYVE-1 Antibody (11C11) [NBP3-26159] - Staining of HepG2 with LYVE-1 Antibody (11C11) at 1:25, 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 505-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26159_rabbit-lyve-1-mab-11c11-28220241249369.jpg "Immunocytochemistry/Immunofluorescence: LYVE-1 Antibody (11C11) [NBP3-26159] - Staining of HepG2 with LYVE-1 Antibody (11C11) at 1:25, 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 505-conjugated Goat Anti-Rabbit IgG (H+L).")
![Flow Cytometry: LYVE-1 Antibody (11C11) [NBP3-26159] - Overlay Peak curve showing HepG2 cells stained with LYVE-1 Antibody (11C11) (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/nbp3-26159_rabbit-lyve-1-mab-11c11-28220241418361.jpg)
![Western Blot: MUPP1 Antibody [NBP1-49974] - Detection of Human MUPP1 by Western Blot and Immunoprecipitation. Samples: Whole cell lysate (5, 15 and 50 mcg for WB; 1 mg for IP, 20% of IP loaded) from HeLa cells. Antibodies: Affinity purified rabbit anti-MUPP1 antibody used for WB at 0.1 mcg/ml (A) and 1 mcg/ml (B) and used for IP at 3 mcg/mg lysate. MUPP1 was also immunoprecipitated by rabbit anti-MUPP1 antibody which recognizes a downstream epitope. For blotting immunoprecipitated MUPP1 was used. Detection: Chemiluminescence with exposure times of 3 minutes (A and B).](http://images.novusbio.com/fullsize/MUPP1-Antibody-Western-Blot-NBP1-49974-img0002.jpg "<b>Independent Antibodies Validation. </b>Western Blot: MUPP1 Antibody [NBP1-49974] - Detection of Human MUPP1 by Western Blot and Immunoprecipitation. Samples: Whole cell lysate (5, 15 and 50 mcg for WB; 1 mg for IP, 20% of IP loaded) from HeLa cells. Antibodies: Affinity purified rabbit anti-MUPP1 antibody used for WB at 0.1 mcg/ml (A) and 1 mcg/ml (B) and used for IP at 3 mcg/mg lysate. MUPP1 was also immunoprecipitated by rabbit anti-MUPP1 antibody which recognizes a downstream epitope. For blotting immunoprecipitated MUPP1 was used. Detection: Chemiluminescence with exposure times of 3 minutes (A and B).")
![Immunohistochemistry: EGF Antibody (18B12) [NBP3-26606] - Image of EGF Antibody (18B12) diluted at 1:100 and staining in paraffin-embedded human skin 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 4C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.66% DAB.](http://images.novusbio.com/fullsize/nbp3-26606_rabbit-egf-mab-18b12-262202414225218.jpg "Immunohistochemistry: EGF Antibody (18B12) [NBP3-26606] - Image of EGF Antibody (18B12) diluted at 1:100 and staining in paraffin-embedded human skin 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 4C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.66% DAB.")
![Flow Cytometry: EGF Antibody (18B12) [NBP3-26606] - Overlay Peak curve showing SH-SY5Y cells stained with EGF Antibody (18B12) (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/nbp3-26606_rabbit-egf-mab-18b12-282202414183693.jpg)
![Immunocytochemistry/Immunofluorescence: DDR2 Antibody [NBP2-56485] - Staining of human cell line BJ shows localization to actin filaments. Antibody staining is shown in green.](http://images.novusbio.com/fullsize/DDR2-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-56485-img0002.jpg "Immunocytochemistry/Immunofluorescence: DDR2 Antibody [NBP2-56485] - Staining of human cell line BJ shows localization to actin filaments. Antibody staining is shown in green.")
![Western Blot: TGFBI Antibody [NBP2-20613] - Sample (30 ug of whole cell lysate) A: Hela 7. 5% SDS PAGE gel, diluted at 1:1000.](http://images.novusbio.com/fullsize/TGFBI-Antibody-Western-Blot-NBP2-20613-img0001.jpg "Western Blot: TGFBI Antibody [NBP2-20613] - Sample (30 ug of whole cell lysate) A: Hela 7. 5% SDS PAGE gel, diluted at 1:1000.")