| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26261-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26579-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26155-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | MAB6333-SP | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| IHC-Prediluted | NBP2-44900 | |||
| Azide and BSA Free | NBP2-34793-0.1mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26679-50ul | |||
![Western Blot: UQCRC2 Antibody (2F6) [NBP3-15182] - Positive WB detected in:HepG2 whole cell lysate, 293 whole cell lysate, U251 whole cell lysate, MCF-7 whole cell lysate. All lanes: UQCRC2 antibody at 1:2000. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 49 KDa. Observed band size: 49 KDa.](http://images.novusbio.com/fullsize/UQCRC2-Antibody-2F6-Western-Blot-NBP3-15182-img0003.jpg "Western Blot: UQCRC2 Antibody (2F6) [NBP3-15182] - Positive WB detected in:HepG2 whole cell lysate, 293 whole cell lysate, U251 whole cell lysate, MCF-7 whole cell lysate. All lanes: UQCRC2 antibody at 1:2000. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 49 KDa. Observed band size: 49 KDa.")
![Immunohistochemistry: UQCRC2 Antibody (2F6) [NBP3-15182] - IHC image of UQCRC2 antibody diluted at 1:100 and staining in paraffin-embedded human liver 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/UQCRC2-Antibody-2F6-Immunohistochemistry-NBP3-15182-img0002.jpg)
![Immunohistochemistry: UQCRC2 Antibody (2F6) [NBP3-15182] - IHC image of UQCRC2 antibody diluted at 1:100 and staining in paraffin-embedded human heart 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/UQCRC2-Antibody-2F6-Immunohistochemistry-NBP3-15182-img0001.jpg)
![Western Blot: NCOA3/AIB1 Antibody [NB100-315] - Detection of human NCOA3/AIB1 (SRC3) by western blot. Samples: Whole cell lysate (50 ug) from HeLa, HEK293T, and Jurkat cells prepared using NETN lysis buffer. Antibody: Affinity purified rabbit anti-NCOA3/AIB1 antibody NB100-315 used for WB at 0.1 ug/ml. Detection: Chemiluminescence with an exposure time of 3 minutes.](http://images.novusbio.com/fullsize/NCOA3-AIB1-Antibody-Western-Blot-NB100-315-img0004.jpg "Western Blot: NCOA3/AIB1 Antibody [NB100-315] - Detection of human NCOA3/AIB1 (SRC3) by western blot. Samples: Whole cell lysate (50 ug) from HeLa, HEK293T, and Jurkat cells prepared using NETN lysis buffer. Antibody: Affinity purified rabbit anti-NCOA3/AIB1 antibody NB100-315 used for WB at 0.1 ug/ml. Detection: Chemiluminescence with an exposure time of 3 minutes.")
![<b>Biological Strategies Validation. </b>Western Blot: NCOA3/AIB1 Antibody [NB100-315] - Detection of Human SRC3 by Western Blot. Samples: Whole cell lysate (50 ug) from HeLa and 293T cells prepared using NETN lysis buffer. Antibody: Affinity purified rabbit anti-SRC3 antibody NB100-315 used for WB at 0.1 ug/ml. Detection: Chemiluminescence with an exposure time of 3 minutes.](http://images.novusbio.com/fullsize/NCOA3-AIB1-Antibody-Western-Blot-NB100-315-img0003.jpg)
![Immunoprecipitation: NCOA3/AIB1 Antibody [NB100-315] - Detection of human NCOA3/AIB1 by western blot of immunoprecipitates. Samples: Whole cell lysate (1.0 mg per IP reaction; 20% of IP loaded) from HeLa cells prepared using NETN lysis buffer. Antibodies: Affinity purified rabbit anti-NCOA3/AIB1 antibody NB100-315 (lot 2) used for IP at 6 ug per reaction. NCOA3/AIB1 was also immunoprecipitated by a previous lot of this antibody (lot 1). For blotting immunoprecipitated NCOA3/AIB1, NB100-315 was used at 1 ug/ml. Detection: Chemiluminescence with an exposure time of 3 minutes.](http://images.novusbio.com/fullsize/NCOA3-AIB1-Antibody-Immunoprecipitation-NB100-315-img0005.jpg)
![Western Blot: USP22 Antibody (18H6) [NBP3-26261] - Positive Western Blot detected in: A549 whole cell lysate, HepG2 whole cell lysate, PC3 whole cell lysate. All lanes: USP22 Antibody at 1: 2000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 60, 59 kDa Observed band size: 55-72 kDa](http://images.novusbio.com/fullsize/nbp3-26261_rabbit-usp22-mab-18h6-282202411472117.jpg "Western Blot: USP22 Antibody (18H6) [NBP3-26261] - Positive Western Blot detected in: A549 whole cell lysate, HepG2 whole cell lysate, PC3 whole cell lysate. All lanes: USP22 Antibody at 1: 2000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 60, 59 kDa Observed band size: 55-72 kDa")
![Immunocytochemistry/Immunofluorescence: USP22 Antibody (18H6) [NBP3-26261] - Staining of Hela cell with USP22 Antibody (18H6) at 1:50, 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 507-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26261_rabbit-usp22-mab-18h6-282202412475133.jpg)
![Flow Cytometry: USP22 Antibody (18H6) [NBP3-26261] - Overlay Peak curve showing Hela cells stained with USP22 Antibody (18H6) (red line) at 1:100. 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/nbp3-26261_rabbit-usp22-mab-18h6-282202414312718.jpg)
![Western Blot: CPT2 Antibody [NBP1-32226] - Sample(30 ug of whole cell lysate)A:HeLa S3 7. 5% SDS PAGE, antibody diluted at 1:1000.](http://images.novusbio.com/fullsize/CPT2-Antibody-Western-Blot-NBP1-32226-img0002.jpg "Western Blot: CPT2 Antibody [NBP1-32226] - Sample(30 ug of whole cell lysate)A:HeLa S3 7. 5% SDS PAGE, antibody diluted at 1:1000.")
![Western Blot: CPT2 Antibody [NBP1-32226] - Various whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with CPT2 antibody [N1C1] (NBP1-32226) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp1-32226_rabbit-polyclonal-cpt2-antibody-91020241959354.jpg)
![Immunohistochemistry: TTC11 Antibody (27B4) [NBP3-26579] - Image of TTC11 Antibody (27B4) diluted at 1:100 and staining in paraffin-embedded human heart 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 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26579_rabbit-ttc11-mab-27b4-2722024845323.jpg "Immunohistochemistry: TTC11 Antibody (27B4) [NBP3-26579] - Image of TTC11 Antibody (27B4) diluted at 1:100 and staining in paraffin-embedded human heart 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 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB.")
![Immunohistochemistry: TTC11 Antibody (27B4) [NBP3-26579] - Image of TTC11 Antibody (27B4) diluted at 1:100 and staining in paraffin-embedded human heart 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 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26579_rabbit-ttc11-mab-27b4-2722024857339.jpg)
![Western Blot: TTC11 Antibody (27B4) [NBP3-26579] - Positive Western Blot detected in: HepG2 whole cell lysate, PC3 whole cell lysate, MCF-7 whole cell lysate, Hela whole cell lysate, U251 whole cell lysate, A549 whole cell lysate. All lanes: TTC11 Antibody at 1: 1000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 17 kDa Observed band size: 17-22 kDa](http://images.novusbio.com/fullsize/nbp3-26579_rabbit-ttc11-mab-27b4-282202411472141.jpg)
![Immunohistochemistry: Monoamine Oxidase B Antibody (9B6) [NBP3-26155] - Image of Monoamine Oxidase B Antibody (9B6) diluted at 1:100 and staining in paraffin-embedded human liver 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 IgG polymer labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26155_rabbit-monoamine-oxidase-b-mab-9b6-262202414471525.jpg "Immunohistochemistry: Monoamine Oxidase B Antibody (9B6) [NBP3-26155] - Image of Monoamine Oxidase B Antibody (9B6) diluted at 1:100 and staining in paraffin-embedded human liver 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 IgG polymer labeled by HRP and visualized using 0.05% DAB.")
![Immunohistochemistry: Monoamine Oxidase B Antibody (9B6) [NBP3-26155] - Image of Monoamine Oxidase B Antibody (9B6) diluted at 1:100 and staining in paraffin-embedded human liver 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 IgG polymer labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26155_rabbit-monoamine-oxidase-b-mab-9b6-26220241522417.jpg)
![Western Blot: Monoamine Oxidase B Antibody (9B6) [NBP3-26155] - Positive Western Blot detected in: L02 whole cell lysate, HepG2 whole cell lysate. All lanes: Monoamine Oxidase B Antibody at 1: 1000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 59, 47 kDa Observed band size: 59 kDa](http://images.novusbio.com/fullsize/nbp3-26155_rabbit-monoamine-oxidase-b-mab-9b6-282202411485834.jpg)
![Immunohistochemistry-Paraffin: CEACAM5/CD66e Antibody (SPM551) [NBP2-33011] - Formalin-paraffin colon stained with CEA MAb (SPM551)](http://images.novusbio.com/fullsize/CEACAM5-CD66e-Antibody-SPM551-Immunohistochemistry-Paraffin-NBP2-33011-img0001.jpg "Immunohistochemistry-Paraffin: CEACAM5/CD66e Antibody (SPM551) [NBP2-33011] - Formalin-paraffin colon stained with CEA MAb (SPM551)")
![Immunohistochemistry: CD46 Antibody (7D12) [NBP3-26679] - Image of CD46 Antibody (7D12) 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/nbp3-26679_rabbit-cd46-mab-7d12-262202415253333.jpg "Immunohistochemistry: CD46 Antibody (7D12) [NBP3-26679] - Image of CD46 Antibody (7D12) 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: CD46 Antibody (7D12) [NBP3-26679] - Image of CD46 Antibody (7D12) 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/nbp3-26679_rabbit-cd46-mab-7d12-262202415355713.jpg)
![Western Blot: CD46 Antibody (7D12) [NBP3-26679] - Positive Western Blot detected in: Hela whole cell lysate. All lanes: CD46 Antibody at 1: 1000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 44, 45, 43, 41, 42, 40, 37 kDa Observed band size: 56 kDa](http://images.novusbio.com/fullsize/nbp3-26679_rabbit-cd46-mab-7d12-282202411472111.jpg)
![Immunohistochemistry-Paraffin: ERRFI1 Antibody [NBP2-16372] - Mouse placenta. ERRFI1 antibody [N1C1] diluted at 1:500.Antigen Retrieval: Citrate buffer, pH 6.0, 15 min.](http://images.novusbio.com/fullsize/ERRFI1-Antibody-Immunohistochemistry-Paraffin-NBP2-16372-img0002.jpg "Immunohistochemistry-Paraffin: ERRFI1 Antibody [NBP2-16372] - Mouse placenta. ERRFI1 antibody [N1C1] diluted at 1:500.Antigen Retrieval: Citrate buffer, pH 6.0, 15 min.")
![Western Blot: ERRFI1 Antibody [NBP2-16372] -Various whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with Mig-6 antibody [N1C1] diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/antibody/nbp2-16372_rabbit-polyclonal-errfi1-antibody-western-blot-5102023105643..jpg)