| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-52551-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB100-2691-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB100-2194-0.025ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-61834-0.025ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-05805-50ul | |||
![Western Blot: p130 Antibody (2C8A8) [NBP2-52551] - Analysis using RBL2 mAb against human RBL2 (AA: 939-1139) recombinant protein. (Expected MW is 48.7 kDa)](http://images.novusbio.com/fullsize/p130-Antibody-2C8A8-Western-Blot-NBP2-52551-img0002.jpg "Western Blot: p130 Antibody (2C8A8) [NBP2-52551] - Analysis using RBL2 mAb against human RBL2 (AA: 939-1139) recombinant protein. (Expected MW is 48.7 kDa)")
![Flow Cytometry: p130 Antibody (2C8A8) [NBP2-52551] - Analysis of Hela cells using RBL2 mouse mAb (green) and negative control (red).](http://images.novusbio.com/fullsize/p130-Antibody-2C8A8-Flow-Cytometry-NBP2-52551-img0001.jpg)
![Western Blot: p130 Antibody (2C8A8) [NBP2-52551] - Analysis using RBL2 mAb against HEK293 (1) and RBL2 (AA: 939-1139)-hIgGFc transfected HEK293 (2) cell lysate.](http://images.novusbio.com/fullsize/p130-Antibody-2C8A8-Western-Blot-NBP2-52551-img0003.jpg)
![ELISA: p130 Antibody (2C8A8) [NBP2-52551] - Black line: Control Antigen (100 ng); Purple line: Antigen(10ng); Blue line: Antigen (50 ng); Red line: Antigen (100 ng).](http://images.novusbio.com/fullsize/p130-Antibody-2C8A8-ELISA-NBP2-52551-img0004.jpg)
![Western Blot: Mcl-1 Antibody (8C6D4B1) [NB100-2194] - Analysis using MCL1 mouse mAb against Hela (1), BCBL-1 (2), Jurkat (3) and HL60 (4) cell lysate.](http://images.novusbio.com/fullsize/Mcl-1-Antibody-8C6D4B1-Western-Blot-NB100-2194-img0008.jpg "Western Blot: Mcl-1 Antibody (8C6D4B1) [NB100-2194] - Analysis using MCL1 mouse mAb against Hela (1), BCBL-1 (2), Jurkat (3) and HL60 (4) cell lysate.")
![Immunocytochemistry/Immunofluorescence: Mcl-1 Antibody (8C6D4B1) [NB100-2194] - Analysis of HepG2 cells using MCL1 mouse mAb (green). Red: Actin filaments have been labeled with DY-554 phalloidin. Blue: DRAQ5 fluorescent DNA dye.](http://images.novusbio.com/fullsize/Mcl-1-Antibody-8C6D4B1-Immunocytochemistry-Immunofluorescence-NB100-2194-img0006.jpg)
![Immunohistochemistry-Paraffin: Mcl-1 Antibody (8C6D4B1) [NB100-2194] - Analysis of human lymphnode tissues using MCL1 mouse mAb with DAB staining.](http://images.novusbio.com/fullsize/Mcl-1-Antibody-8C6D4B1-Immunohistochemistry-Paraffin-NB100-2194-img0007.jpg)
![Western Blot: mGluR2 Antibody (6E4F6) [NBP2-61834] - Analysis using GRM2 mouse mAb against SK-N-SH (1), Jurkat (2), and SW620 (3) cell lysate.](http://images.novusbio.com/fullsize/mGluR2-Antibody-6E4F6-Western-Blot-NBP2-61834-img0004.jpg "Western Blot: mGluR2 Antibody (6E4F6) [NBP2-61834] - Analysis using GRM2 mouse mAb against SK-N-SH (1), Jurkat (2), and SW620 (3) cell lysate.")
![Western Blot: mGluR2 Antibody (6E4F6) [NBP2-61834] - Analysis using GRM2 mAb against human GRM2 (AA: extra 414-558) recombinant protein. (Expected MW is 42.4 kDa)](http://images.novusbio.com/fullsize/mGluR2-Antibody-6E4F6-Western-Blot-NBP2-61834-img0003.jpg)
![Western Blot: mGluR2 Antibody (6E4F6) [NBP2-61834] - Analysis using GRM2 mAb against HEK293 (1) and GRM2 (AA: extra 414-558)-hIgGFc transfected HEK293 (2) cell lysate.](http://images.novusbio.com/fullsize/mGluR2-Antibody-6E4F6-Western-Blot-NBP2-61834-img0005.jpg)
![ELISA: mGluR2 Antibody (6E4F6) [NBP2-61834] - Black line: Control Antigen (100 ng);Purple line: Antigen (10ng); Blue line: Antigen (50 ng); Red line:Antigen (100 ng)](http://images.novusbio.com/fullsize/mGluR2-Antibody-6E4F6-ELISA-NBP2-61834-img0001.jpg)
![ELISA: mGluR2 Antibody (6E4F6) [NBP2-61834] - Analysis of SK-N-SH cells using GRM2 mouse mAb (green) and negative control (red).](http://images.novusbio.com/fullsize/mGluR2-Antibody-6E4F6-ELISA-NBP2-61834-img0002.jpg)
![Flow Cytometry: Park7/DJ-1 Antibody (007) [NBP3-05805] - Flow cytometric analysis of Human Park7/DJ-1 expression on HeLa cells. The cells were treated, stained with NBP3-05805, then a FITC-conjugated second step antibody. The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of intact cells.](http://images.novusbio.com/fullsize/nbp3-05805_rabbit-monoclonal-park7-dj-1-antibody-007-235202521451748.png "Flow Cytometry: Park7/DJ-1 Antibody (007) [NBP3-05805] - Flow cytometric analysis of Human Park7/DJ-1 expression on HeLa cells. The cells were treated, stained with NBP3-05805, then a FITC-conjugated second step antibody. The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of intact cells.")
![Immunocytochemistry/ Immunofluorescence: Park7/DJ-1 Antibody (007) [NBP3-05805] - Immunofluorescence staining of Human Park7/DJ-1 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 NBP3-05805 (1:60) at 37 1 hour. Then cells were stained with the Alexa Fluor 594-conjugated Goat Anti-rabbit IgG secondary antibody (red) and counterstained with DAPI (blue). Positive staining was localized to cytoplasm.](http://images.novusbio.com/fullsize/nbp3-05805_rabbit-monoclonal-park7-dj-1-antibody-007-23520251628125.png)
![Western Blot: Park7/DJ-1 Antibody (007) [NBP3-05805] - NBP3-05805 at 1:1000 dilution Lane A: Hela Whole Cell Lysate Lane B: Jurkat 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:20 kDa Observed band size:24 kDa](http://images.novusbio.com/fullsize/nbp3-05805_rabbit-monoclonal-park7-dj-1-antibody-007-23520252135168.png)
![Immunoprecipitation: Park7/DJ-1 Antibody (007) [NBP3-05805] - PARK7 was immunoprecipitated using: Lane A:0.5 mg Jurkat Whole Cell Lysate Lane B:0.5 mg Hela Whole Cell Lysate Lane C:0.5 mg 293T Whole Cell Lysate 2 uL NBP3-05805 and 15 ul of 50 % Protein G agarose. Primary antibody: NBP3-05805, 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: 20 kDa Observed band size: 20 kDa](http://images.novusbio.com/fullsize/nbp3-05805_rabbit-monoclonal-park7-dj-1-antibody-007-235202514331514.png)
![Western Blot: Bcl-2 Antibody (9F3-R) [NBP3-32072] - Western blot analysis of Bcl-2 on different lysates with Mouse anti-Bcl-2 antibody (NBP3-32072) at 1/1,000 dilution. Lane 1: THP-1 cell lysate Lane 2: HL-60 cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 26 kDa Observed band size: 26 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 (NBP3-32072) at 1/1,000 dilution was used in 5% NFDM/TBST at 4C 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/nbp3-32072_mouse-bcl-2-mab-9f3-r-278202415212474.jpg "Western Blot: Bcl-2 Antibody (9F3-R) [NBP3-32072] - Western blot analysis of Bcl-2 on different lysates with Mouse anti-Bcl-2 antibody (NBP3-32072) at 1/1,000 dilution. Lane 1: THP-1 cell lysate Lane 2: HL-60 cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 26 kDa Observed band size: 26 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 (NBP3-32072) at 1/1,000 dilution was used in 5% NFDM/TBST at 4C overnight. Goat Anti-Mouse IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: Bcl-2 Antibody (9F3-R) [NBP3-32072] - Immunohistochemical analysis of paraffin-embedded human tonsil tissue with Mouse anti-Bcl-2 antibody (NBP3-32072) 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 (NBP3-32072) 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/nbp3-32072_mouse-bcl-2-mab-9f3-r-298202414333630.jpg)
![Flow Cytometry: Bcl-2 Antibody (9F3-R) [NBP3-32072] - Flow cytometric analysis of THP-1 cells labeling Bcl-2. Cells were fixed and permeabilized. Then stained with the primary antibody (NBP3-32072, 1μg/mL) (red) compared with Mouse IgG1 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-Mouse 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/nbp3-32072_mouse-bcl-2-mab-9f3-r-29202416372125.jpg)
![Western Blot: FADD Antibody (JE45-25) [NBP3-32328] - Western blot analysis of FADD on different lysates with Rabbit anti-FADD antibody (NBP3-32328) at 1/1,000 dilution. Lane 1: A431 cell lysate, 10 ug/Lane Lane 2: K-562 cell lysate, 10 ug/Lane Lane 3: Jurkat cell lysate, 10 ug/Lane Lane 4: MCF7 cell lysate, 10 ug/Lane Lane 5: HeLa cell lysate, 10 ug/Lane Lane 6: SK-Br-3 cell lysate, 10 ug/Lane Lane 7: SW480 cell lysate, 10 ug/Lane Lane 8: THP-1 cell lysate, 10 ug/Lane Lane 9: A549 cell lysate, 10 ug/Lane Lane 10: HepG2 cell lysate, 10 ug/Lane Predicted band size: 23 kDa Observed band size: 25 kDa Exposure time: 90 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 (NBP3-32328) 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 1:200,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32328_rabbit-fadd-mab-je45-25-278202416331258.jpg "Western Blot: FADD Antibody (JE45-25) [NBP3-32328] - Western blot analysis of FADD on different lysates with Rabbit anti-FADD antibody (NBP3-32328) at 1/1,000 dilution. Lane 1: A431 cell lysate, 10 ug/Lane Lane 2: K-562 cell lysate, 10 ug/Lane Lane 3: Jurkat cell lysate, 10 ug/Lane Lane 4: MCF7 cell lysate, 10 ug/Lane Lane 5: HeLa cell lysate, 10 ug/Lane Lane 6: SK-Br-3 cell lysate, 10 ug/Lane Lane 7: SW480 cell lysate, 10 ug/Lane Lane 8: THP-1 cell lysate, 10 ug/Lane Lane 9: A549 cell lysate, 10 ug/Lane Lane 10: HepG2 cell lysate, 10 ug/Lane Predicted band size: 23 kDa Observed band size: 25 kDa Exposure time: 90 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 (NBP3-32328) 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 1:200,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: FADD Antibody (JE45-25) [NBP3-32328] - Immunohistochemical analysis of paraffin-embedded human stomach tissue with Rabbit anti-FADD antibody (NBP3-32328) at 1/200 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 (NBP3-32328) at 1/200 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/nbp3-32328_rabbit-fadd-mab-je45-25-298202413585545.jpg)
![Immunocytochemistry/ Immunofluorescence: FADD Antibody (JE45-25) [NBP3-32328] - Immunocytochemistry analysis of SW480 cells labeling FADD with Rabbit anti-FADD antibody (NBP3-32328) at 1/50 dilution. Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.05% Triton X-100 in PBS for 20 minutes, and then blocked with 2% negative goat serum for 30 minutes at room temperature. Cells were then incubated with Rabbit anti-FADD antibody (NBP3-32328) at 1/50 dilution in 2% negative goat serum overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. 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/nbp3-32328_rabbit-fadd-mab-je45-25-29202410484813.jpg)
![Western Blot: p16INK4a/CDKN2A Antibody (PD01-16) [NBP3-32688] - Western blot analysis of p16INK4a/CDKN2A on different lysates with Mouse anti-p16INK4a/CDKN2A antibody (NBP3-32688) at 1/1,000 dilution. Lane 1: HeLa cell lysate Lane 2: HepG2 cell lysate Lane 3: HEK-293 cell lysate Lane 4: NIH:OVCAR-3 cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 16 kDa Observed band size: 16 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 (NBP3-32688) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Mouse IgG - HRP Secondary Antibody at 1:100,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32688_mouse-p16ink4a-cdkn2a-mab-pd01-16-2882024142262.jpg "Western Blot: p16INK4a/CDKN2A Antibody (PD01-16) [NBP3-32688] - Western blot analysis of p16INK4a/CDKN2A on different lysates with Mouse anti-p16INK4a/CDKN2A antibody (NBP3-32688) at 1/1,000 dilution. Lane 1: HeLa cell lysate Lane 2: HepG2 cell lysate Lane 3: HEK-293 cell lysate Lane 4: NIH:OVCAR-3 cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 16 kDa Observed band size: 16 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 (NBP3-32688) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Mouse IgG - HRP Secondary Antibody at 1:100,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: p16INK4a/CDKN2A Antibody (PD01-16) [NBP3-32688] - Immunohistochemical analysis of paraffin-embedded human tonsil tissue with Mouse anti-p16INK4a/CDKN2A antibody (NBP3-32688) at 1/500 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 (NBP3-32688) 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/nbp3-32688_mouse-p16ink4a-cdkn2a-mab-pd01-16-29820241426269.jpg)
![Immunocytochemistry/ Immunofluorescence: p16INK4a/CDKN2A Antibody (PD01-16) [NBP3-32688] - Immunocytochemistry analysis of HeLa cells labeling p16INK4a/CDKN2A with Mouse anti-p16INK4a/CDKN2AINK4a/CDKN2A antibody (NBP3-32688) 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-p16INK4a/CDKN2A antibody (NBP3-32688) 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/nbp3-32688_mouse-p16ink4a-cdkn2a-mab-pd01-16-29202410334055.jpg)
![Flow Cytometry: Cyclin B1 Antibody (V152) [NBP3-07017] - Separation of JURKAT cells stained using anti-Cyclin B1 (V152) purified antibody (concentration in sample 5.0 ug/mL, GAM APC, red-filled) from JURKAT cells unstained by primary antibody (GAM APC, black-dashed) in flow cytometry analysis (intracellular staining).](http://images.novusbio.com/fullsize/Cyclin-B1-Antibody-V152-Flow-Cytometry-NBP3-07017-img0001.jpg "Flow Cytometry: Cyclin B1 Antibody (V152) [NBP3-07017] - Separation of JURKAT cells stained using anti-Cyclin B1 (V152) purified antibody (concentration in sample 5.0 ug/mL, GAM APC, red-filled) from JURKAT cells unstained by primary antibody (GAM APC, black-dashed) in flow cytometry analysis (intracellular staining).")
![Western Blot: eIF5A2 Antibody (1E7) [H00056648-M01] - Analysis of EIF5A2 expression in transfected 293T cell line by EIF5A2 monoclonal antibody (M01), clone 1E7.Lane 1: EIF5A2 transfected lysate(16.8 KDa).Lane 2: Non-transfected lysate.](http://images.novusbio.com/fullsize/eIF5A2-Antibody-1E7-Western-Blot-H00056648-M01-img0003.jpg "Western Blot: eIF5A2 Antibody (1E7) [H00056648-M01] - Analysis of EIF5A2 expression in transfected 293T cell line by EIF5A2 monoclonal antibody (M01), clone 1E7.Lane 1: EIF5A2 transfected lysate(16.8 KDa).Lane 2: Non-transfected lysate.")
![Sandwich ELISA: eIF5A2 Antibody (1E7) [H00056648-M01] - Detection limit for recombinant GST tagged EIF5A2 is approximately 0.1ng/ml as a capture antibody.](http://images.novusbio.com/fullsize/eIF5A2-Antibody-1E7-Sandwich-ELISA-H00056648-M01-img0002.jpg)
![In vitro assay: Recombinant Human SOD1/Cu-Zn SOD Pre-formed Fibrils Protein [NBP3-14783] - Thioflavin T assay of SOD1 pre-formed fibrils (PFFs) (NBP3-14783) combined with SOD1 monomers . Pre-formed fibrils seed the aggregation of monomers, leading to an increase in Thioflavin T fluorescence](http://images.novusbio.com/fullsize/Recombinant-Human-SOD1-Cu-Zn-SOD-Pre-formed-Fibrils-Protein-In-vitro-assay-NBP3-14783-img0001.jpg "In vitro assay: Recombinant Human SOD1/Cu-Zn SOD Pre-formed Fibrils Protein [NBP3-14783] - Thioflavin T assay of SOD1 pre-formed fibrils (PFFs) (NBP3-14783) combined with SOD1 monomers . Pre-formed fibrils seed the aggregation of monomers, leading to an increase in Thioflavin T fluorescence")
![Electron Microscopy: Recombinant Human SOD1/Cu-Zn SOD Pre-formed Fibrils Protein [NBP3-14783] - TEM of human SOD1 pre-formed fibrils (PFFs)](http://images.novusbio.com/fullsize/Recombinant Human SOD1-Cu-Zn SOD Pre-formed Fibrils Protein-Electron Microscopy-NBP3-14783-img0003.jpg)
![Electron Microscopy: Recombinant Human SOD1/Cu-Zn SOD Pre-formed Fibrils Protein [NBP3-14783] - TEM of human SOD1 pre-formed fibrils (PFFs)](http://images.novusbio.com/fullsize/Recombinant-Human-SOD1-Cu-Zn-SOD-Pre-formed-Fibrils-Protein-Electron-Microscopy-NBP3-14783-img0002.jpg)