| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-00295-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-90222-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-89374-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-90247-50ul | |||
![Immunohistochemistry-Paraffin: FHIT Antibody [NBP3-00295] - Immunochemical staining of human FHIT in human lung cancer with NBP3-00295 (1:1000, formalin-fixed paraffin embedded sections).](http://images.novusbio.com/fullsize/nbp3-00295_rabbit-polyclonal-fhit-antibody-235202514331511.png "Immunohistochemistry-Paraffin: FHIT Antibody [NBP3-00295] - Immunochemical staining of human FHIT in human lung cancer with NBP3-00295 (1:1000, formalin-fixed paraffin embedded sections).")
![Immunohistochemistry-Paraffin: FHIT Antibody [NBP3-00295] - Immunochemical staining of human FHIT in human breast carcinoma with NBP3-00295 (1:1000, formalin-fixed paraffin embedded sections).](http://images.novusbio.com/fullsize/nbp3-00295_rabbit-polyclonal-fhit-antibody-23520251633505.png)
![Immunocytochemistry/ Immunofluorescence: FHIT Antibody [NBP3-00295] - Immunofluorescence staining of 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 NBP3-00295 (1:1000) at 4 overnight. Then cells were stained with the Alexa Fluor488-conjugated Goat Anti-rabbit IgG secondary antibody (green).Positive staining was localized to cytoplasm and nucleus.](http://images.novusbio.com/fullsize/nbp3-00295_rabbit-polyclonal-fhit-antibody-23520251129352.png)
![Western Blot: Phosphoserine phosphatase Antibody (001) [NBP2-90222] - Anti-PSPH rabbit monoclonal antibody at 1:500 dilution. Lane A: MCF7 Whole Cell Lysate. Lane B: K562 Whole Cell Lysate. Lane C: HepG2 Whole Cell Lysate. Lysates/proteins at 30 ug per lane. Secondary: Goat Anti-Rabbit IgG H&L (Dylight800) at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size:25 kDa. Observed band size:27 kDa](http://images.novusbio.com/fullsize/Phosphoserine-phosphatase-Antibody-001-Western-Blot-NBP2-90222-img0004.jpg "Western Blot: Phosphoserine phosphatase Antibody (001) [NBP2-90222] - Anti-PSPH rabbit monoclonal antibody at 1:500 dilution. Lane A: MCF7 Whole Cell Lysate. Lane B: K562 Whole Cell Lysate. Lane C: HepG2 Whole Cell Lysate. Lysates/proteins at 30 ug per lane. Secondary: Goat Anti-Rabbit IgG H&L (Dylight800) at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size:25 kDa. Observed band size:27 kDa")
![Immunoprecipitation: Phosphoserine phosphatase Antibody (001) [NBP2-90222] - PSPH was immunoprecipitated using: Lane A:0.5 mg K562 Whole Cell Lysate. Lane B:0.5 mg HepG2 Whole Cell Lysate. 0.5 uL anti-PSPH rabbit monoclonal antibody and 15 ul of 50 % Protein G agarose. Primary antibody: Anti-PSPH rabbit monoclonal antibody,at 1:1000 dilution. Secondary antibody: Dylight 800-labeled antibody to rabbit IgG (H+L), at 1:5000 dilution. Developed using the odssey technique. Performed under reducing conditions.Predicted band size: 25 kDa. Observed band size: 25 kDa.](http://images.novusbio.com/fullsize/Phosphoserine-phosphatase-Antibody-001-Immunoprecipitation-NBP2-90222-img0002.jpg)
![Immunocytochemistry/Immunofluorescence: Phosphoserine phosphatase Antibody (001) [NBP2-90222] - Immunofluorescence staining of Human PSPH in A549 cells. Cells were fixed with 4% PFA, permeabilzed with 0.3% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP2-90222 antibody (dilution ratio 1:60) at 4? overnight. Then cells were stained with the Alexa Fluor(R) 594-conjugated Goat Anti-rabbit IgG secondary antibody (red) and counterstained with DAPI (blue).](http://images.novusbio.com/fullsize/nbp2-90222_rabbit-monoclonal-phosphoserine-phosphatase-antibody-001-235202511444476.png)
![Western Blot: PADI4 Antibody (PSH01-33) [NBP3-32707] - Western blot analysis of PADI4 on different lysates with Rabbit anti-PADI4 antibody (NBP3-32707) at 1/1,000 dilution. Lane 1: 293T overexpress PADI4 whole cell lysate Lane 2: 293T whole cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 74 kDa Observed band size: 74 kDa Exposure time: 1 minute; 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 (NBP3-32707) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:100,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32707_rabbit-padi4-mab-psh01-33-278202415295544.jpg "Western Blot: PADI4 Antibody (PSH01-33) [NBP3-32707] - Western blot analysis of PADI4 on different lysates with Rabbit anti-PADI4 antibody (NBP3-32707) at 1/1,000 dilution. Lane 1: 293T overexpress PADI4 whole cell lysate Lane 2: 293T whole cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 74 kDa Observed band size: 74 kDa Exposure time: 1 minute; 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 (NBP3-32707) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:100,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: PADI4 Antibody (PSH01-33) [NBP3-32707] - Immunohistochemical analysis of paraffin-embedded human spleen tissue with Rabbit anti-PADI4 antibody (NBP3-32707) at 1/1,000 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 (NBP3-32707) 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/nbp3-32707_rabbit-padi4-mab-psh01-33-298202414161870.jpg)
![Western Blot: FABP3/H-FABP Antibody (JE53-37) [NBP3-32325] - Western blot analysis of FABP3/H-FABP on different lysates with Rabbit anti-FABP3/H-FABP antibody (NBP3-32325) at 1/2,000 dilution. Lane 1: Mouse heart tissue lysate Lane 2: Rat heart tissue lysate Lysates/proteins at 30 ug/Lane. Predicted band size: 14 kDa Observed band size: 14 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 (NBP3-32325) at 1/2,000 dilution was used in 5% NFDM/TBST at 4C overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32325_rabbit-fabp3-h-fabp-mab-je53-37-278202416285235.jpg "Western Blot: FABP3/H-FABP Antibody (JE53-37) [NBP3-32325] - Western blot analysis of FABP3/H-FABP on different lysates with Rabbit anti-FABP3/H-FABP antibody (NBP3-32325) at 1/2,000 dilution. Lane 1: Mouse heart tissue lysate Lane 2: Rat heart tissue lysate Lysates/proteins at 30 ug/Lane. Predicted band size: 14 kDa Observed band size: 14 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 (NBP3-32325) at 1/2,000 dilution was used in 5% NFDM/TBST at 4C overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: FABP3/H-FABP Antibody (JE53-37) [NBP3-32325] - Immunohistochemical analysis of paraffin-embedded human heart tissue with Rabbit anti-FABP3/H-FABP antibody (NBP3-32325) at 1/100 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 (NBP3-32325) at 1/100 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/nbp3-32325_rabbit-fabp3-h-fabp-mab-je53-37-29820241435241.jpg)
![Western Blot: Cytochrome P450 1A2 Antibody (JE39-22) [NBP3-32241] - Western blot analysis of Cytochrome P450 1A2 on HepG2 cell lysates with Rabbit anti-Cytochrome P450 1A2 antibody (NBP3-32241) at 1/1,000 dilution. Lysates/proteins at 10 ug/Lane. Predicted band size: 58 kDa Observed band size: 50 kDa Exposure time: 2 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 (NBP3-32241) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:100,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32241_rabbit-cytochrome-p450-1a2-mab-je39-22-278202415295537.jpg "Western Blot: Cytochrome P450 1A2 Antibody (JE39-22) [NBP3-32241] - Western blot analysis of Cytochrome P450 1A2 on HepG2 cell lysates with Rabbit anti-Cytochrome P450 1A2 antibody (NBP3-32241) at 1/1,000 dilution. Lysates/proteins at 10 ug/Lane. Predicted band size: 58 kDa Observed band size: 50 kDa Exposure time: 2 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 (NBP3-32241) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:100,000 dilution was used for 1 hour at room temperature.")
![Immunocytochemistry/ Immunofluorescence: Cytochrome P450 1A2 Antibody (JE39-22) [NBP3-32241] - Immunocytochemistry analysis of HepG2 cells labeling Cytochrome P450 1A2 with Rabbit anti-Cytochrome P450 1A2 antibody (NBP3-32241) at 1/250 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 Rabbit anti-Cytochrome P450 1A2 antibody (NBP3-32241) at 1/250 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit 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-Mouse IgG H&L (iFluor™ 594) was used as the secondary antibody at 1/1,000 dilution.](http://images.novusbio.com/fullsize/nbp3-32241_rabbit-cytochrome-p450-1a2-mab-je39-22-2920241192349.jpg)
![Flow Cytometry: Cytochrome P450 1A2 Antibody (JE39-22) [NBP3-32241] - Flow cytometric analysis of HepG2 cells labeling Cytochrome P450 1A2. Cells were fixed and permeabilized. Then stained with the primary antibody (NBP3-32241, 1ug/ml) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).](http://images.novusbio.com/fullsize/nbp3-32241_rabbit-cytochrome-p450-1a2-mab-je39-22-39202488467.jpg)
![Western Blot: Leukotriene A4 Hydrolase/LTA4H Antibody (201) [NBP2-89374] - Lane A: Hela Whole Cell Lysate Lane B: A549 Whole Cell Lysate Lane C: 293T Whole Cell Lysate Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG H&L (Dylight800) at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size:69 kDa Observed band size:69 kDa](http://images.novusbio.com/fullsize/Leukotriene-A4-Hydrolase-LTA4H-Antibody-201-Western-Blot-NBP2-89374-img0002.jpg "Western Blot: Leukotriene A4 Hydrolase/LTA4H Antibody (201) [NBP2-89374] - Lane A: Hela Whole Cell Lysate Lane B: A549 Whole Cell Lysate Lane C: 293T Whole Cell Lysate Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG H&L (Dylight800) at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size:69 kDa Observed band size:69 kDa")
![Immunoprecipitation: Leukotriene A4 Hydrolase/LTA4H Antibody (201) [NBP2-89374] - Lane A:0.5 mg Hela Whole Cell Lysate Lane B:0.5 mg 293T Whole Cell Lysate0.5 uL anti-LTA4H rabbit monoclonal antibody and 15 ul of 50 % Protein G agarose. Primary antibody: Anti-LTA4H rabbit monoclonal antibody,at 1:500 dilution Secondary antibody: Dylight 800-labeled antibody to rabbit IgG (H+L), at 1:5000 dilution Developed using the odssey technique. Performed under reducing conditions.Predicted band size: 110 kDa Observed band size: 110 kDa](http://images.novusbio.com/fullsize/Leukotriene-A4-Hydrolase-LTA4H-Antibody-201-Immunoprecipitation-NBP2-89374-img0003.jpg)
![Immunocytochemistry/Immunofluorescence: Leukotriene A4 Hydrolase/LTA4H Antibody (201) [NBP2-89374] - Staining of Human LTA4H 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 NBP2-89374 (1:300) at 4c overnight. Then cells were stained with the Alexa Fluor(R) 488-conjugated Goat Anti-rabbit IgG secondary antibody (green) and counterstained with DAPI (blue). Positive staining was localized to cytoplasm.](http://images.novusbio.com/fullsize/nbp2-89374_rabbit-monoclonal-leukotriene-a4-hydrolase-lta4h-antibody-201-235202512205518.png)
![Immunohistochemistry-Paraffin: PSGL-1/CD162 Antibody (031) [NBP2-90247] - Staining of human SELPLG in human tonsil with rabbit monoclonal antibody (1:200).](http://images.novusbio.com/fullsize/PSGL-1-CD162-Antibody-031-Immunohistochemistry-Paraffin-NBP2-90247-img0003.jpg "Immunohistochemistry-Paraffin: PSGL-1/CD162 Antibody (031) [NBP2-90247] - Staining of human SELPLG in human tonsil with rabbit monoclonal antibody (1:200).")
![Flow Cytometry: PSGL-1/CD162 Antibody (031) [NBP2-90247] - Analysis of Human SELPLG(CD162) expression on human whole blood granulocytes. Cells were stained with purified anti-Human SELPLG(CD162), then a FITC-conjugated second step antibody. The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of viable granulocytes.](http://images.novusbio.com/fullsize/PSGL-1-CD162-Antibody-031-Flow-Cytometry-NBP2-90247-img0002.jpg)
![Immunohistochemistry-Paraffin: PSGL-1/CD162 Antibody (031) [NBP2-90247] - Staining of human SELPLG in human spleen with rabbit monoclonal antibody (1:200).](http://images.novusbio.com/fullsize/PSGL-1-CD162-Antibody-031-Immunohistochemistry-Paraffin-NBP2-90247-img0001.jpg)
![Western Blot: Caveolin-1 [p Tyr14] Antibody (M283) [NBP3-23246] - Western blot image of human A431 cells unstimulated (lanes 1, 3, & 5) or stimulated with pervanadate (1 mM) for 30 min (lanes 2, 4, & 6). The blots were probed with rabbit polyclonal caveolin-1 (N-term.) (lanes 1 & 2), mouse monoclonal caveolin-1 (Tyr-14) (lanes 3 & 4) or mouse monoclonal caveolin-1 (lanes 5 & 6).](http://images.novusbio.com/fullsize/nbp3-23246_mouse-caveolin-1-p-tyr14-mab-m283-19920231856942.jpg "Western Blot: Caveolin-1 [p Tyr14] Antibody (M283) [NBP3-23246] - Western blot image of human A431 cells unstimulated (lanes 1, 3, & 5) or stimulated with pervanadate (1 mM) for 30 min (lanes 2, 4, & 6). The blots were probed with rabbit polyclonal caveolin-1 (N-term.) (lanes 1 & 2), mouse monoclonal caveolin-1 (Tyr-14) (lanes 3 & 4) or mouse monoclonal caveolin-1 (lanes 5 & 6).")
![Immunocytochemistry/Immunofluorescence: Caveolin-1 [p Tyr14] Antibody (M283) [NBP3-23246] - Immunocytochemical labeling of caveolin-1 phosphorylation in rabbit spleen fibroblasts. The cells were treated with pervanadate (1 mM) for 30 min, then fixed with paraformaldehyde and labeled with rabbit polyclonal Caveolin-1 (N-terminal region) and mouse monoclonal Caveolin-1 (Tyr-14) antibodies. The antibodies were detected using appropriate secondary antibodies conjugated to Cy3.](http://images.novusbio.com/fullsize/nbp3-23246_mouse-caveolin-1-p-tyr14-mab-m283-199202312523624.jpg)