| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-59617 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| IHC-Prediluted | NBP2-48119 | |||
| Azide and BSA Free | NBP3-11499 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26542-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26218-50ul | |||
| Conjugate | Catalog # | Availability | Size | Price |
|---|---|---|---|---|
| Alexa Fluor 488 | DDX0321A488-100 | |||
| Alexa Fluor 546 | DDX0321A546-100 | |||
| Alexa Fluor 647 | DDX0321A647-100 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-54509-100ug | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26568-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26422-50ul | |||
![Protein Array: S100A1 Antibody (S100A1/1942) [NBP2-59615] - containing more than 19,000 full-length human proteins. Z- and S- Score: The Z-score represents the strength of a signal that an antibody (in combination with a fluorescently-tagged anti-IgG secondary) produces when binding to a particular protein on the HuProt array. Z-scores are described in units of standard deviations above the mean value of all signals generated on that array. If targets on HuProt are arranged in descending order of the Z-score, the S-score is the difference between the Z-score. S-score therefore represents the relative target specificity of an Ab to its intended target. An Ab is considered to specific to its intended target, if the Ab has an S-score of at least 2.5. For example, if Ab binds to protein X with a Z-score of 43 and to protein Y with a Z-score of 14, then the S-score for the binding of that Ab to protein X is equal to 29](http://images.novusbio.com/fullsize/S100A1-Antibody-S100A1-1942-Protein-Array-NBP2-59615-img0003.jpg "Protein Array: S100A1 Antibody (S100A1/1942) [NBP2-59615] - containing more than 19,000 full-length human proteins. Z- and S- Score: The Z-score represents the strength of a signal that an antibody (in combination with a fluorescently-tagged anti-IgG secondary) produces when binding to a particular protein on the HuProt array. Z-scores are described in units of standard deviations above the mean value of all signals generated on that array. If targets on HuProt are arranged in descending order of the Z-score, the S-score is the difference between the Z-score. S-score therefore represents the relative target specificity of an Ab to its intended target. An Ab is considered to specific to its intended target, if the Ab has an S-score of at least 2.5. For example, if Ab binds to protein X with a Z-score of 43 and to protein Y with a Z-score of 14, then the S-score for the binding of that Ab to protein X is equal to 29")
![Immunohistochemistry-Paraffin: S100A1 Antibody (S100A1/1942) [NBP2-59615] - Formalin-fixed, paraffin-embedded human Melanoma stained with S100A1 Antibody (S100A1/1942).](http://images.novusbio.com/fullsize/S100A1-Antibody-S100A1-1942-Immunohistochemistry-Paraffin-NBP2-59615-img0004.jpg)
![Immunohistochemistry-Paraffin: S100A1 Antibody (S100A1/1942) [NBP2-59615] - Formalin-fixed, paraffin-embedded human Melanoma stained with S100A1 Mouse Monoclonal Antibody (S100A1/1942)](http://images.novusbio.com/fullsize/S100A1-Antibody-S100A1-1942-Immunohistochemistry-Paraffin-NBP2-59615-img0001.jpg)
![Immunohistochemistry-Paraffin: Tyrosinase Antibody (T311 + OCA1/812) [NBP2-44686] - Formalin-fixed, paraffin-embedded human melanoma stained with Tyrosinase Mouse Monoclonal Antibody (T311 + OCA1/812).](http://images.novusbio.com/fullsize/Tyrosinase-Antibody-T311-+-OCA1-812-Immunohistochemistry-Paraffin-NBP2-44686-img0002.jpg "Immunohistochemistry-Paraffin: Tyrosinase Antibody (T311 + OCA1/812) [NBP2-44686] - Formalin-fixed, paraffin-embedded human melanoma stained with Tyrosinase Mouse Monoclonal Antibody (T311 + OCA1/812).")
![Immunohistochemistry-Paraffin: Tyrosinase Antibody (T311 + OCA1/812) [NBP2-44686] - Melanoma stained with Tyrosinase Monoclonal Antibody (T311 + OCA1/812).](http://images.novusbio.com/fullsize/Tyrosinase-Antibody-T311-+-OCA1-812-Immunohistochemistry-Paraffin-NBP2-44686-img0001.jpg)
![Immunohistochemistry: GSK-3 beta Antibody (9G11) [NBP3-26542] - Image of GSK-3 beta Antibody (9G11) 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/nbp3-26542_rabbit-gsk-3-beta-mab-9g11-262202414471519.jpg "Immunohistochemistry: GSK-3 beta Antibody (9G11) [NBP3-26542] - Image of GSK-3 beta Antibody (9G11) 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.")
![Western Blot: GSK-3 beta Antibody (9G11) [NBP3-26542] - Positive Western Blot detected in: Hela whole cell lysate, HepG2 whole cell lysate, A549 whole cell lysate, 293 whole cell lysate. All lanes: GSK3 beta Antibody at 1: 1000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 47, 49 kDa Observed band size: 47 kDa](http://images.novusbio.com/fullsize/nbp3-26542_rabbit-gsk-3-beta-mab-9g11-28220241140910.jpg)
![Immunocytochemistry/Immunofluorescence: GSK-3 beta Antibody (9G11) [NBP3-26542] - Staining of Hela Cells with GSK-3 beta Antibody (9G11) 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/nbp3-26542_rabbit-gsk-3-beta-mab-9g11-282202412475130.jpg)
![Immunohistochemistry: HSD3B1 Antibody (10G2) [NBP3-26218] - Image of HSD3B1 Antibody (10G2) diluted at 1:100 and staining in paraffin-embedded human placenta 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 0.50% DAB.](http://images.novusbio.com/fullsize/nbp3-26218_rabbit-hsd3b1-mab-10g2-2622024152246.jpg "Immunohistochemistry: HSD3B1 Antibody (10G2) [NBP3-26218] - Image of HSD3B1 Antibody (10G2) diluted at 1:100 and staining in paraffin-embedded human placenta 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 0.50% DAB.")
![Immunohistochemistry: HSD3B1 Antibody (10G2) [NBP3-26218] - Image of HSD3B1 Antibody (10G2) diluted at 1:100 and staining in paraffin-embedded human placenta 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 0.50% DAB.](http://images.novusbio.com/fullsize/nbp3-26218_rabbit-hsd3b1-mab-10g2-2722024856317.jpg)
![Immunocytochemistry/Immunofluorescence: HSD3B1 Antibody (10G2) [NBP3-26218] - Staining of Hela with HSD3B1 Antibody (10G2) 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 514-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26218_rabbit-hsd3b1-mab-10g2-282202412475114.jpg)
![Flow Cytometry: HSD3B1 Antibody (10G2) [NBP3-26218] - Overlay Peak curve showing 293 cells stained with HSD3B1 Antibody (10G2) (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/nbp3-26218_rabbit-hsd3b1-mab-10g2-282202414183666.jpg)
![Flow Cytometry: CD39/ENTPD1 Antibody (AC2.5) [DDX0321P-100]](http://images.novusbio.com/fullsize/CD39-ENTPD1-Antibody-AC2-5-Flow-Cytometry-DDX0321P-100-img0001.jpg "Flow Cytometry: CD39/ENTPD1 Antibody (AC2.5) [DDX0321P-100]")
![Immunohistochemistry-Paraffin: CFTR Antibody (CFTR/1643) [NBP2-53375] - Formalin-fixed, paraffin-embedded Human Pancreas stained with CFTR Monoclonal Antibody (CFTR/1643).](http://images.novusbio.com/fullsize/CFTR-Antibody-CFTR-1643-Immunohistochemistry-Paraffin-NBP2-53375-img0001.jpg "Immunohistochemistry-Paraffin: CFTR Antibody (CFTR/1643) [NBP2-53375] - Formalin-fixed, paraffin-embedded Human Pancreas stained with CFTR Monoclonal Antibody (CFTR/1643).")
![Flow Cytometry: CFTR Antibody (CFTR/1643) [NBP2-53375] - Analysis of MOLT-4 cells using CFTR Antibody (CFTR/1643) followed by goat anti-Mouse IgG-CF488 (Blue); Isotype Control (Red).](http://images.novusbio.com/fullsize/CFTR-Antibody-CFTR-1643-Flow-Cytometry-NBP2-53375-img0002.jpg)
![Protein Array: CFTR Antibody (CFTR/1643) [NBP2-53375] - Analysis of Protein Array containing >19,000 full-length human proteins using CFTR Antibody (CFTR/1643) Z- and S- Score: The Z-score represents the strength of a signal that a monoclonal antibody (Monoclonal Antibody) (in combination with a fluorescently-tagged anti-IgG secondary antibody) produces when binding to a particular protein on the HuProt(TM) array. Z-scores are described in units of standard deviations (SD's) above the mean value of all signals generated on that array. If targets on HuProt(TM) are arranged in descending order of the Z-score, the S-score is the difference (also in units of SD's) between the Z-score. S-score therefore represents the relative target specificity of a Monoclonal Antibody to its intended target. A Monoclonal Antibody is considered to specific to its intended target, if the Monoclonal Antibody has an S-score of at least 2.5.](http://images.novusbio.com/fullsize/CFTR-Antibody-CFTR-1643-Protein-Array-NBP2-53375-img0003.jpg)
![Immunohistochemistry: Ferritin Antibody (12H1) [NBP3-26568] - Image of Ferritin Antibody (12H1) diluted at 1:50 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 4°C overnight. The primary is detected by a Goat anti-Mouse IgG labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26568_mouse-ferritin-mab-12h1-26220241447157.jpg "Immunohistochemistry: Ferritin Antibody (12H1) [NBP3-26568] - Image of Ferritin Antibody (12H1) diluted at 1:50 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 4°C overnight. The primary is detected by a Goat anti-Mouse IgG labeled by HRP and visualized using 0.05% DAB.")
![Immunohistochemistry: Ferritin Antibody (12H1) [NBP3-26568] - Image of Ferritin Antibody (12H1) diluted at 1:50 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 4°C overnight. The primary is detected by a Goat anti-Mouse IgG labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26568_mouse-ferritin-mab-12h1-27220248573313.jpg)
![Western Blot: Ferritin Antibody (12H1) [NBP3-26568] - Positive Western Blot detected in: U251 whole cell lysate, JK whole cell lysate. All lanes: Ferritin Antibody at 1: 500 Secondary: Goat polyclonal to mouse IgG at 1/50000 dilution. Predicted band size: 22 kDa Observed band size: 22 kDa](http://images.novusbio.com/fullsize/nbp3-26568_mouse-ferritin-mab-12h1-282202411485815.jpg)
![Flow Cytometry: Ferritin Antibody (12H1) [NBP3-26568] - Overlay Peak curve showing 293 cells stained with Ferritin Antibody (12H1) (red line) at 1:50. Then 10% normal goat serum was Incubated to block non-specific protein-protein interactions followed by the antibody (1ug/1*10^6 cells) for 45 min at 4C. The secondary antibody used was FITC-conjugated Goat Anti-Mouse IgG (H+L) at 1/200 dilution for 35 min at 4C. Isotype control antibody (green line) was mouse IgG1 (1ug/1*10^6 cells) used under the same conditions. Acquisition of >10,000 events was performed.](http://images.novusbio.com/fullsize/nbp3-26568_mouse-ferritin-mab-12h1-282202414312738.jpg)
![Western Blot: Citidine Deaminase Antibody [NBP1-31412] - A. 50 ug mouse kidney lysate/extract 15% SDS-PAGE Citidine Deaminase antibody dilution: 1:500 The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/Citidine-Deaminase-Antibody-Western-Blot-NBP1-31412-img0006.jpg "Western Blot: Citidine Deaminase Antibody [NBP1-31412] - A. 50 ug mouse kidney lysate/extract 15% SDS-PAGE Citidine Deaminase antibody dilution: 1:500 The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.")
![Immunohistochemistry-Paraffin: Citidine Deaminase Antibody [NBP1-31412] - Paraffin-embedded Gastric CA N87 xenograft, using antibody at 1:100 dilution.](http://images.novusbio.com/fullsize/Citidine-Deaminase-Antibody-Immunohistochemistry-Paraffin-NBP1-31412-img0003.jpg)
![Western Blot: Citidine Deaminase Antibody [NBP1-31412] - Various whole cell extracts (30 ug) were separated by 15% SDS-PAGE, and the membrane was blotted with Citidine Deaminase antibody (NBP1-31412) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp1-31412_rabbit-polyclonal-citidine-deaminase-antibody-9102024205684.jpg)
![Immunohistochemistry-Paraffin: PRAS40 Antibody [NBP2-19924] - Immunohistochemical analysis of paraffin-embedded Hepatoma, using antibody at 1:500 dilution.](http://images.novusbio.com/fullsize/PRAS40-Antibody-Immunohistochemistry-Paraffin-NBP2-19924-img0003.jpg "Immunohistochemistry-Paraffin: PRAS40 Antibody [NBP2-19924] - Immunohistochemical analysis of paraffin-embedded Hepatoma, using antibody at 1:500 dilution.")
![Western Blot: Protein Phosphatase 1C gamma Antibody [NB110-40551] - Whole cell lysate (50 mcg for WB; 1 mg for IP, 20% of IP loaded) from HeLa cells. NB110-40551 used for WB at 0.1 mcg/ml (A) and 1 mcg/ml (B) and used for IP at 3 mcg/mg lysate (B). PPP1CB was also immunoprecipitated by NB110-40551.](http://images.novusbio.com/fullsize/Protein-Phosphatase-1C-gamma-Antibody-Western-Blot-NB110-40551-img0002.jpg "Western Blot: Protein Phosphatase 1C gamma Antibody [NB110-40551] - Whole cell lysate (50 mcg for WB; 1 mg for IP, 20% of IP loaded) from HeLa cells. NB110-40551 used for WB at 0.1 mcg/ml (A) and 1 mcg/ml (B) and used for IP at 3 mcg/mg lysate (B). PPP1CB was also immunoprecipitated by NB110-40551.")
![Immunohistochemistry-Paraffin: Protein Phosphatase 1C gamma Antibody [NB110-40551] - Human breast carcinoma. Antibody: Affinity purified rabbit anti- PPP1CC used at a dilution of 1:1,000 (1ug/ml). Detection: DAB](http://images.novusbio.com/fullsize/Protein-Phosphatase-1C-gamma-Antibody-Immunohistochemistry-Paraffin-NB110-40551-img0010.jpg)
![Immunohistochemistry: GSK-3 beta [p Ser9] Antibody (3A6) [NBP3-26422] - Image of GSK-3 beta [p Ser9] Antibody (3A6) 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 4C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.](http://images.novusbio.com/fullsize/nbp3-26422_rabbit-gsk-3-beta-p-ser-9-mab-3a6-26220241525330.jpg "Immunohistochemistry: GSK-3 beta [p Ser9] Antibody (3A6) [NBP3-26422] - Image of GSK-3 beta [p Ser9] Antibody (3A6) 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 4C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.")
![Western Blot: GSK-3 beta [p Ser9] Antibody (3A6) [NBP3-26422] - Positive Western Blot detected in Hela whole cell lysate, 293 whole cell lysate, A549 whole cell lysate (treated with Calyculin A or not). All lanes: GSK-3 beta [p Ser9] Antibody at 0.77ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 46 KDa Observed band size: 46 KDa](http://images.novusbio.com/fullsize/nbp3-26422_rabbit-gsk-3-beta-p-ser-9-mab-3a6-28220241136300.jpg)
![Immunocytochemistry/Immunofluorescence: GSK-3 beta [p Ser9] Antibody (3A6) [NBP3-26422] - Staining of Hela cells(treated with 50mM Calyculin A for 30min) with GSK-3 beta [p Ser9] Antibody (3A6) at 1:100, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 488-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26422_rabbit-gsk-3-beta-p-ser-9-mab-3a6-28220241312216.jpg)