| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| IHC-Prediluted | NBP2-48165 | |||
| Azide and BSA Free | NBP3-11463 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| IHC-Prediluted | NBP2-44329 | |||
| Azide and BSA Free | NBP2-34740-0.1mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26499-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-47735-0.1mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-49873-0.1mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26504-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26692-50ul | |||
![Immunohistochemistry-Paraffin: MAGE 1 Antibody (MZ2E/838) [NBP2-44508] - Human Testicular Carcinoma stained with MAGE-1 Monoclonal Antibody (MZ2E/838).](http://images.novusbio.com/fullsize/MAGE-1-Antibody-MZ2E-838-Immunohistochemistry-Paraffin-NBP2-44508-img0001.jpg "Immunohistochemistry-Paraffin: MAGE 1 Antibody (MZ2E/838) [NBP2-44508] - Human Testicular Carcinoma stained with MAGE-1 Monoclonal Antibody (MZ2E/838).")
![Immunoprecipitation: FBXW7/Cdc4 Antibody [NB100-88138] - Whole cell lysate (1.0 mg per IP reaction; 20% of IP loaded) from HeLa cells prepared using NETN lysis buffer. NB100-88138 used for IP at 6 ug per reaction. FBXW7/Cdc4 was also immunoprecipitated by a previous lot of this antibody. For blotting immunoprecipitated FBXW7/Cdc4, NB100-88138 was used at 0.1 ug/ml. Detected by chemiluminescence with an exposure time of 10 seconds.](http://images.novusbio.com/fullsize/FBXW7-Cdc4-Antibody-Immunoprecipitation-NB100-88138-img0001.jpg "Immunoprecipitation: FBXW7/Cdc4 Antibody [NB100-88138] - Whole cell lysate (1.0 mg per IP reaction; 20% of IP loaded) from HeLa cells prepared using NETN lysis buffer. NB100-88138 used for IP at 6 ug per reaction. FBXW7/Cdc4 was also immunoprecipitated by a previous lot of this antibody. For blotting immunoprecipitated FBXW7/Cdc4, NB100-88138 was used at 0.1 ug/ml. Detected by chemiluminescence with an exposure time of 10 seconds.")
![Immunohistochemistry-Paraffin: Myogenin Antibody (SPM144) [NBP2-32987] - Formalin-fixed paraffin-embedded human Rhabdomyosarcoma stained with Myogenin Monoclonal Antibody (SPM144)](http://images.novusbio.com/fullsize/Myogenin-Antibody-SPM144-Immunohistochemistry-Paraffin-NBP2-32987-img0001.jpg "Immunohistochemistry-Paraffin: Myogenin Antibody (SPM144) [NBP2-32987] - Formalin-fixed paraffin-embedded human Rhabdomyosarcoma stained with Myogenin Monoclonal Antibody (SPM144)")
![Western Blot: ROCK2 Antibody (10E1) [NBP3-15152] - Positive WB detected in: Hela whole cell lysate, MCF-7 whole cell lysate, L02 whole cell lysate, HepG2 whole cell lysate, Mouse Brain whole cell lysate, Rat Brain whole cell lysate. All lanes: ROCK2 antibody at 1:1000. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 161 KDa. Observed band size: 161 KDa.](http://images.novusbio.com/fullsize/ROCK2-Antibody-10E1-Western-Blot-NBP3-15152-img0002.jpg "Western Blot: ROCK2 Antibody (10E1) [NBP3-15152] - Positive WB detected in: Hela whole cell lysate, MCF-7 whole cell lysate, L02 whole cell lysate, HepG2 whole cell lysate, Mouse Brain whole cell lysate, Rat Brain whole cell lysate. All lanes: ROCK2 antibody at 1:1000. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 161 KDa. Observed band size: 161 KDa.")
![Immunocytochemistry/Immunofluorescence: ROCK2 Antibody (10E1) [NBP3-15152] - Immunofluorescence staining of Hela Cells with at ROCK2 antibody 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeated by 0.2% TritonX-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/ROCK2-Antibody-10E1-Immunocytochemistry-Immunofluorescence-NBP3-15152-img0001.jpg)
![Western Blot: GRB2 Antibody (6E1) [NBP3-15167] - Positive WB detected in: Hela whole cell lysate, MCF-7 whole cell lysate, Mouse Brain whole cell lysate, Rat Brain whole cell lysate. All lanes: GRB2 antibody at 1:1000. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 26, 21 KDa. Observed band size: 28 KDa.](http://images.novusbio.com/fullsize/GRB2-Antibody-6E1-Western-Blot-NBP3-15167-img0002.jpg "Western Blot: GRB2 Antibody (6E1) [NBP3-15167] - Positive WB detected in: Hela whole cell lysate, MCF-7 whole cell lysate, Mouse Brain whole cell lysate, Rat Brain whole cell lysate. All lanes: GRB2 antibody at 1:1000. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 26, 21 KDa. Observed band size: 28 KDa.")
![Immunohistochemistry: GRB2 Antibody (6E1) [NBP3-15167] - IHC image of GRB2 antibody diluted at 1:100 and staining in paraffin-embedded human ovarian 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/GRB2-Antibody-6E1-Immunohistochemistry-NBP3-15167-img0001.jpg)
![Immunohistochemistry: Argininosuccinate Synthase Antibody (18G11) [NBP3-26499] - Image of Argininosuccinate Synthase Antibody (18G11) diluted at 1:100 and staining in paraffin-embedded human kidney 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 0.56% DAB.](http://images.novusbio.com/fullsize/nbp3-26499_rabbit-argininosuccinate-synthase-mab-18g11-262202415475626.jpg "Immunohistochemistry: Argininosuccinate Synthase Antibody (18G11) [NBP3-26499] - Image of Argininosuccinate Synthase Antibody (18G11) diluted at 1:100 and staining in paraffin-embedded human kidney 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 0.56% DAB.")
![Immunocytochemistry/Immunofluorescence: Argininosuccinate Synthase Antibody (18G11) [NBP3-26499] - Staining of Hela with Argininosuccinate Synthase Antibody (18G11) 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 516-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26499_rabbit-argininosuccinate-synthase-mab-18g11-28220241247517.jpg)
![Flow Cytometry: Argininosuccinate Synthase Antibody (18G11) [NBP3-26499] - Overlay Peak curve showing Jurkat cells stained with Argininosuccinate Synthase Antibody (18G11) (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/nbp3-26499_rabbit-argininosuccinate-synthase-mab-18g11-282202414312780.jpg)
![Immunohistochemistry-Paraffin: FSH beta Antibody (SPM107) [NBP2-45133] - Human Pituitary stained with FSH-beta Monoclonal Antibody (SPM107).](http://images.novusbio.com/fullsize/FSH-beta-Antibody-SPM107-Immunohistochemistry-Paraffin-NBP2-45133-img0001.jpg "Immunohistochemistry-Paraffin: FSH beta Antibody (SPM107) [NBP2-45133] - Human Pituitary stained with FSH-beta Monoclonal Antibody (SPM107).")
![Immunohistochemistry-Paraffin: SPIN1 Antibody [NBP3-41330] - Used in DAB staining on fromalin fixed paraffin- embedded Kidney tissue](http://images.novusbio.com/fullsize/nbp3-41330_rabbit-spin1-pab-612202421175952.jpg "Immunohistochemistry-Paraffin: SPIN1 Antibody [NBP3-41330] - Used in DAB staining on fromalin fixed paraffin- embedded Kidney tissue")
![Western Blot: SPIN1 Antibody [NBP3-41330] - Sample: Recombinant SPIN1, Human.](http://images.novusbio.com/fullsize/nbp3-41330_rabbit-spin1-pab-612202421175976.jpg)
![Immunohistochemistry-Paraffin: CD20 Antibody (IGEL/1497R) [NBP2-49872] - Formalin-fixed, paraffin-embedded human Tonsil stained with CD20 Antibody (IGEL/1497R).](http://images.novusbio.com/fullsize/CD20-Antibody-IGEL-1497R-Immunohistochemistry-Paraffin-NBP2-49872-img0003.jpg "Immunohistochemistry-Paraffin: CD20 Antibody (IGEL/1497R) [NBP2-49872] - Formalin-fixed, paraffin-embedded human Tonsil stained with CD20 Antibody (IGEL/1497R).")
![Flow Cytometry: CD20 Antibody (IGEL/1497R) [NBP2-49872] - Flow Cytometric Analysis of Raji cells. CD20 Antibody (IGEL/1497R) followed by Goat anti-Mouse IgG-CF488 (Blue); Isotype Control (Red).](http://images.novusbio.com/fullsize/CD20-Antibody-IGEL-1497R-Flow-Cytometry-NBP2-49872-img0002.jpg)
![Immunohistochemistry: Apolipoprotein A-II/ApoA2 Antibody (6H2) [NBP3-26504] - Image of Apolipoprotein A-II/ApoA2 Antibody (6H2) diluted at 1:87.5 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 biotinylated secondary antibody and visualized using an HRP conjugated SP system.](http://images.novusbio.com/fullsize/nbp3-26504_rabbit-apolipoprotein-a-ii-apoa2-mab-6h2-2722024850462.jpg "Immunohistochemistry: Apolipoprotein A-II/ApoA2 Antibody (6H2) [NBP3-26504] - Image of Apolipoprotein A-II/ApoA2 Antibody (6H2) diluted at 1:87.5 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 biotinylated secondary antibody and visualized using an HRP conjugated SP system.")
![Western Blot: Apolipoprotein A-II/ApoA2 Antibody (6H2) [NBP3-26504] - Positive Western Blot detected in: 293T whole cell lysate, A549 whole cell lysate. All lanes: Apolipoprotein A-II/ApoA2 Antibody at 0.87ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 12 KDa Observed band size: 12 KDa](http://images.novusbio.com/fullsize/nbp3-26504_rabbit-apolipoprotein-a-ii-apoa2-mab-6h2-28220241147215.jpg)
![Flow Cytometry: Apolipoprotein A-II/ApoA2 Antibody (6H2) [NBP3-26504] - Overlay histogram showing A549 cells stained with Apolipoprotein A-II/ApoA2 Antibody (6H2) (red line) at 1:50. The cells were fixed with 70% Ethylalcohol (18h) and then permeabilized with 0.3% Triton X-100 for 2 min. The cells were then incubated in 1x PBS /10% normal goat serum to block non-specific protein-protein interactions followed by primary antibody for 1 h at 4C. The secondary antibody used was FITC goat anti-rabbit IgG (H+L) at 1/200 dilution for 1 h at 4C. Control antibody (green line) was used under the same conditions. Acquisition of >10,000 events was performed.](http://images.novusbio.com/fullsize/nbp3-26504_rabbit-apolipoprotein-a-ii-apoa2-mab-6h2-282202414312783.jpg)
![Western Blot: Retinoic Acid Receptor gamma Antibody [NBP2-15098] - A. 30 ug A549 whole cell lysate/extract, B. 30 ug HCT116 whole cell lysate/extract 10 % SDS-PAGE gel, antibody dilution 1:1000.](http://images.novusbio.com/fullsize/Retinoic-Acid-Receptor-gamma-Antibody-Western-Blot-NBP2-15098-img0002.jpg "Western Blot: Retinoic Acid Receptor gamma Antibody [NBP2-15098] - A. 30 ug A549 whole cell lysate/extract, B. 30 ug HCT116 whole cell lysate/extract 10 % SDS-PAGE gel, antibody dilution 1:1000.")
![Western Blot: Retinoic Acid Receptor gamma Antibody [NBP2-15098] - 30 ug Neuro2A whole cell lysate/extract 10% SDS-PAGE gel, antibody dilution 1:1000.](http://images.novusbio.com/fullsize/Retinoic-Acid-Receptor-gamma-Antibody-Western-Blot-NBP2-15098-img0001.jpg)
![Western Blot: RAR gamma/NR1B3 Antibody [NBP2-15098] - Whole cell extract (30 ug) was separated by 10% SDS-PAGE, and the membrane was blotted with RAR gamma/NR1B3 antibody (NBP2-15098) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp2-15098_rabbit-polyclonal-rar-gamma-nr1b3-antibody-910202420104490.jpg)
![Immunohistochemistry: Cyclin E1 Antibody (3A5) [NBP3-26692] - Image of Cyclin E1 Antibody (3A5) 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/nbp3-26692_rabbit-cyclin-e1-mab-3a5-262202414471591.jpg "Immunohistochemistry: Cyclin E1 Antibody (3A5) [NBP3-26692] - Image of Cyclin E1 Antibody (3A5) 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: Cyclin E1 Antibody (3A5) [NBP3-26692] - Image of Cyclin E1 Antibody (3A5) 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/nbp3-26692_rabbit-cyclin-e1-mab-3a5-262202415253332.jpg)
![Immunocytochemistry/Immunofluorescence: Cyclin E1 Antibody (3A5) [NBP3-26692] - Staining of Hela Cells with Cyclin E1 Antibody (3A5) 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/nbp3-26692_rabbit-cyclin-e1-mab-3a5-282202412493621.jpg)