| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB600-1490SS | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-90283-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-11912-25ug | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-90090-50ul | |||
![Western Blot: FTO Antibody (5-2H10) [NBP2-29512] - Western blot of rat testes lysate showing specific immunolabeling of the ~ 58k Fto protein.](http://images.novusbio.com/fullsize/FTO-Antibody-5-2H10-Western-Blot-NBP2-29512-img0002.jpg "Western Blot: FTO Antibody (5-2H10) [NBP2-29512] - Western blot of rat testes lysate showing specific immunolabeling of the ~ 58k Fto protein.")
![Immunocytochemistry/ Immunofluorescence: PTEN [p Ser380] Antibody (JJ08-81) [NBP3-32791] - ICC staining of PTEN in Hela cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the primary antibody (NBP3-32791, 1/100) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue).](http://images.novusbio.com/fullsize/nbp3-32791_rabbit-pten-p-ser380-mab-jj08-81-2920241192374.jpg "Immunocytochemistry/ Immunofluorescence: PTEN [p Ser380] Antibody (JJ08-81) [NBP3-32791] - ICC staining of PTEN in Hela cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the primary antibody (NBP3-32791, 1/100) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue).")
![Immunocytochemistry/ Immunofluorescence: PI 3-Kinase p85 alpha Antibody (A3-D0-R) [NBP3-32817] - Immunocytochemistry analysis of U-937 cells labeling PI 3-Kinase p85 alpha with Mouse anti-PI 3-Kinase p85 alpha antibody (NBP3-32817) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Mouse anti-PI 3-Kinase p85 alpha antibody (NBP3-32817) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Mouse IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI. beta Tubulin (red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Rabbit IgG H&L (iFluor™ 594) were used as the secondary antibody at 1/1,000 dilution.](http://images.novusbio.com/fullsize/nbp3-32817_mouse-pi-3-kinase-p85-alpha-mab-a3-d0-r-29202410484840.jpg "Immunocytochemistry/ Immunofluorescence: PI 3-Kinase p85 alpha Antibody (A3-D0-R) [NBP3-32817] - Immunocytochemistry analysis of U-937 cells labeling PI 3-Kinase p85 alpha with Mouse anti-PI 3-Kinase p85 alpha antibody (NBP3-32817) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Mouse anti-PI 3-Kinase p85 alpha antibody (NBP3-32817) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Mouse IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI. beta Tubulin (red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Rabbit IgG H&L (iFluor™ 594) were used as the secondary antibody at 1/1,000 dilution.")
![Western Blot: PI 3-Kinase p85 alpha Antibody (A3-D0-R) [NBP3-32817] - Western blot analysis of PI 3-Kinase p85 alpha on different lysates with Mouse anti-PI 3-Kinase p85 alpha antibody (NBP3-32817) at 1/5,000 dilution. Lane 1: SW480 cell lysate Lane 2: A431 cell lysate Lane 3: 293T cell lysate Lane 4: Jurkat cell lysate Lane 5: Raji cell lysate Lane 6: MCF7 cell lysate Lane 7: A549 cell lysate Lysates/proteins at 15 µg/Lane. Predicted band size: 84 kDa Observed band size: 84 kDa Exposure time: 1 minute 40 seconds; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody at 1/5,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Mouse IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32817_mouse-pi-3-kinase-p85-alpha-mab-a3-d0-r-3920248485023.jpg)
![Western Blot: PER2 Antibody (JE33-79) [NBP3-32735] - Western blot analysis of PER2 on K562 cell lysates with Rabbit anti-PER2 antibody (NBP3-32735) at 1/500 dilution. Lysates/proteins at 10 ug/Lane. Predicted band size: 137 kDa Observed band size: 180 kDa Exposure time: 1 minute; 8% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32735) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:200,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32735_rabbit-per2-mab-je33-79-278202416331229.jpg "Western Blot: PER2 Antibody (JE33-79) [NBP3-32735] - Western blot analysis of PER2 on K562 cell lysates with Rabbit anti-PER2 antibody (NBP3-32735) at 1/500 dilution. Lysates/proteins at 10 ug/Lane. Predicted band size: 137 kDa Observed band size: 180 kDa Exposure time: 1 minute; 8% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32735) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:200,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: PER2 Antibody (JE33-79) [NBP3-32735] - Immunohistochemical analysis of paraffin-embedded human lung carcinoma tissue with Rabbit anti-PER2 antibody (NBP3-32735) at 1/400 dilution. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (NBP3-32735) at 1/400 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.](http://images.novusbio.com/fullsize/nbp3-32735_rabbit-per2-mab-je33-79-29820241358556.jpg)
![Western Blot: FHIT Antibody (104) [NBP2-90283] - Anti-FHIT rabbit monoclonal antibody at 1:500 dilution. Lane A: HL-60 Whole Cell Lysate. Lysates/proteins at 30 µg per lane. Secondary: Goat Anti-Rabbit IgG H&L (Dylight800) at 1/10000 dilution. Performed under reducing conditions. Predicted band size:17 kDa Observed band size:20 kDa.](http://images.novusbio.com/fullsize/FHIT-Antibody-104-Western-Blot-NBP2-90283-img0001.jpg "Western Blot: FHIT Antibody (104) [NBP2-90283] - Anti-FHIT rabbit monoclonal antibody at 1:500 dilution. Lane A: HL-60 Whole Cell Lysate. Lysates/proteins at 30 µg per lane. Secondary: Goat Anti-Rabbit IgG H&L (Dylight800) at 1/10000 dilution. Performed under reducing conditions. Predicted band size:17 kDa Observed band size:20 kDa.")
![Immunocytochemistry/Immunofluorescence: FHIT Antibody (104) [NBP2-90283] - Immunofluorescence staining of Human FHIT in Hela cells. Cells were fixed with 4% PFA, permeabilzed with 0.3% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP2-90283 antibody (1:300) at 4C overnight. Then cells were stained with the Alexa Fluor(TM) 488-conjugated Goat Anti-rabbit IgG secondary antibody (green).](http://images.novusbio.com/fullsize/nbp2-90283_rabbit-monoclonal-fhit-antibody-104-235202514371347.png)
![Western Blot: Cytochrome P450 1A2 Antibody (F16 P2 D8) [NBP3-11912] - Left: Western blot using CYP2A6 antibody on recombinant cytochrome p450 at 1 ug/ml. Right: Staining using CYP2A6 antibody on normal human liver tissue at 1 ug/ml.](http://images.novusbio.com/fullsize/Cytochrome-P450-1A2-Antibody-F16-P2-D8-Western-Blot-NBP3-11912-img0001.jpg "Western Blot: Cytochrome P450 1A2 Antibody (F16 P2 D8) [NBP3-11912] - Left: Western blot using CYP2A6 antibody on recombinant cytochrome p450 at 1 ug/ml. Right: Staining using CYP2A6 antibody on normal human liver tissue at 1 ug/ml.")
![Western Blot: Glutathione Peroxidase 3/GPX3 Antibody [NBP2-82233] - WB Suggested Anti-GPX3 Antibody Titration: 0.2-1 ug/ml. Positive Control: HepG2 cell lysateGPX3 is strongly supported by BioGPS gene expression data to be expressed in Human HepG2 cells](http://images.novusbio.com/fullsize/Glutathione-Peroxidase-3-GPX3-Antibody-Western-Blot-NBP2-82233-img0002.jpg "Western Blot: Glutathione Peroxidase 3/GPX3 Antibody [NBP2-82233] - WB Suggested Anti-GPX3 Antibody Titration: 0.2-1 ug/ml. Positive Control: HepG2 cell lysateGPX3 is strongly supported by BioGPS gene expression data to be expressed in Human HepG2 cells")
![Immunohistochemistry-Paraffin: Glutathione Peroxidase 3/GPX3 Antibody [NBP2-82233] - Rabbit Anti-GPX3 Antibody. Formalin Fixed Paraffin Embedded Tissue: Human Lung Tissue. Observed Staining: Membrane and cytoplasmic in alveolar type I & II cells. Primary Antibody Concentration: 1:100. Other Working Concentrations: 1/600. Secondary Antibod](http://images.novusbio.com/fullsize/Glutathione-Peroxidase-3-GPX3-Antibody-Immunohistochemistry-Paraffin-NBP2-82233-img0001.jpg)
![Western Blot: Arginase 1/ARG1/liver Arginase Antibody (PD00-05) [NBP3-32047] - Western blot analysis of Arginase 1/ARG1/liver Arginase on human liver tissue lysates with Rabbit anti-Arginase 1/ARG1/liver Arginase antibody (NBP3-32047) at 1/500 dilution. Lysates/proteins at 20 ug/Lane. Predicted band size: 35 kDa Observed band size: 39 kDa Exposure time: 1 minute; 12% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32047) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:300,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32047_rabbit-arginase-1-arg1-liver-arginase-mab-pd00-05-278202415212470.jpg "Western Blot: Arginase 1/ARG1/liver Arginase Antibody (PD00-05) [NBP3-32047] - Western blot analysis of Arginase 1/ARG1/liver Arginase on human liver tissue lysates with Rabbit anti-Arginase 1/ARG1/liver Arginase antibody (NBP3-32047) at 1/500 dilution. Lysates/proteins at 20 ug/Lane. Predicted band size: 35 kDa Observed band size: 39 kDa Exposure time: 1 minute; 12% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32047) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:300,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: Arginase 1/ARG1/liver Arginase Antibody (PD00-05) [NBP3-32047] - Immunohistochemical analysis of paraffin-embedded human liver tissue with Rabbit anti-Arginase 1/ARG1/liver Arginase antibody (NBP3-32047) at 1/1,000 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (NBP3-32047) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.](http://images.novusbio.com/fullsize/nbp3-32047_rabbit-arginase-1-arg1-liver-arginase-mab-pd00-05-29820241420969.jpg)
![Western Blot: PER2 Antibody [NBP2-88036] - WB Suggested Anti-PER2 Antibody Titration: 0.2-1 ug/ml. ELISA Titer: 1:12500. Positive Control: Human Placenta](http://images.novusbio.com/fullsize/PER2-Antibody-Western-Blot-NBP2-88036-img0002.jpg "Western Blot: PER2 Antibody [NBP2-88036] - WB Suggested Anti-PER2 Antibody Titration: 0.2-1 ug/ml. ELISA Titer: 1:12500. Positive Control: Human Placenta")
![Western Blot: PER2 Antibody [NBP2-88036] - Host: Rabbit. Target Name: PER2. Sample Tissue: Human THP-1 Whole Cell. Antibody Dilution: 2ug/ml](http://images.novusbio.com/fullsize/PER2-Antibody-Western-Blot-NBP2-88036-img0001.jpg)
![Western Blot: PER2 Antibody [NBP2-88036] - Host: Rabbit. Target Name: PER2. Sample Type: Human Hela. Antibody Dilution: 1.0ug/ml](http://images.novusbio.com/fullsize/PER2-Antibody-Western-Blot-NBP2-88036-img0003.jpg)
![Immunohistochemistry: ACSL3 Antibody (A8F6-R) [NBP3-31994] - Immunohistochemical analysis of paraffin-embedded human stomach tissue with Mouse anti-ACSL3 antibody (NBP3-31994) at 1/500 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (NBP3-31994) at 1/500 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.](http://images.novusbio.com/fullsize/nbp3-31994_mouse-acsl3-mab-a8f6-r-29820241435265.jpg "Immunohistochemistry: ACSL3 Antibody (A8F6-R) [NBP3-31994] - Immunohistochemical analysis of paraffin-embedded human stomach tissue with Mouse anti-ACSL3 antibody (NBP3-31994) at 1/500 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (NBP3-31994) at 1/500 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.")
![Western Blot: ACSL3 Antibody (A8F6-R) [NBP3-31994] - Western blot analysis of ACSL3 on different lysates with Mouse anti-ACSL3 antibody (NBP3-31994) at 1/1,000 dilution. Lane 1: HeLa cell lysate Lane 2: K-562 cell lysate Lane 3: A431 cell lysate Lane 4: 293T cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 80 kDa Observed band size: 70 kDa Exposure time: 3 minutes; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-31994) at 1/1,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Mouse IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-31994_mouse-acsl3-mab-a8f6-r-3920248485019.jpg)
![Immunohistochemistry-Paraffin: Carbonic Anhydrase VB/CA5B Antibody (008) [NBP2-90090] - Staining of human CA5B in human placenta with rabbit monoclonal antibody (1:100).](http://images.novusbio.com/fullsize/Carbonic-Anhydrase-VB-CA5B-Antibody-008-Immunohistochemistry-Paraffin-NBP2-90090-img0003.jpg "Immunohistochemistry-Paraffin: Carbonic Anhydrase VB/CA5B Antibody (008) [NBP2-90090] - Staining of human CA5B in human placenta with rabbit monoclonal antibody (1:100).")
![Immunohistochemistry-Paraffin: Carbonic Anhydrase VB/CA5B Antibody (008) [NBP2-90090] - Staining of human CA5B in human kidney with rabbit monoclonal antibody (1:100).](http://images.novusbio.com/fullsize/Carbonic-Anhydrase-VB-CA5B-Antibody-008-Immunohistochemistry-Paraffin-NBP2-90090-img0001.jpg)
![Immunohistochemistry-Paraffin: Carbonic Anhydrase VB/CA5B Antibody (008) [NBP2-90090] - Staining of human CA5B in human lung with rabbit monoclonal antibody (1:100).](http://images.novusbio.com/fullsize/Carbonic-Anhydrase-VB-CA5B-Antibody-008-Immunohistochemistry-Paraffin-NBP2-90090-img0002.jpg)