| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-06087-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-89832-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-89345-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-89620-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-90425-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-81048-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-75909SS | |||
![Western Blot: Latexin Antibody (8E1G6C1D4) [NBP3-06087] - Anti-LXN mouse monoclonal antibody at 1:500 dilution Lane A: A549 Whole Cell Lysate Lysates/proteins at 30 ug per lane. Secondary: Goat Anti-Mouse IgG H&L (Dylight800) at 115000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size:26 kDa Observed band size:26 kDa](http://images.novusbio.com/fullsize/Latexin-Antibody-8E1G6C1D4-Western-Blot-NBP3-06087-img0001.jpg "Western Blot: Latexin Antibody (8E1G6C1D4) [NBP3-06087] - Anti-LXN mouse monoclonal antibody at 1:500 dilution Lane A: A549 Whole Cell Lysate Lysates/proteins at 30 ug per lane. Secondary: Goat Anti-Mouse IgG H&L (Dylight800) at 115000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size:26 kDa Observed band size:26 kDa")
![Immunoprecipitation: Latexin Antibody (8E1G6C1D4) [NBP3-06087] - LXN was immunoprecipitated using: Lane A: 0.5 mg MCF-7 Whole Cell Lysate 0.5 uL anti-LXN mouse monoclonal antibody and 15 ul of 50 % Protein G agarose. Primary antibody: Anti-LXN mouse monoclonal antibody, at 1:500 dilution Secondary antibody: Dylight 800-labeled antibody to Mouse IgG (H+L), at 1:7500 dilution Developed using the odssey technique.Performed under reducing conditions.Predicted band size: 25.7 kDa Observed band size: 27 kDa](http://images.novusbio.com/fullsize/Latexin-Antibody-8E1G6C1D4-Immunoprecipitation-NBP3-06087-img0002.jpg)
![Immunohistochemistry-Paraffin: Reg4 Antibody (244) [NBP2-89832] - Staining of human REG4 in human small intestine with rabbit monoclonal antibody at 1:200 dilution.](http://images.novusbio.com/fullsize/Reg4-Antibody-244-Immunohistochemistry-Paraffin-NBP2-89832-img0002.jpg "Immunohistochemistry-Paraffin: Reg4 Antibody (244) [NBP2-89832] - Staining of human REG4 in human small intestine with rabbit monoclonal antibody at 1:200 dilution.")
![Immunohistochemistry-Paraffin: Reg4 Antibody (244) [NBP2-89832] - Staining of human REG4 in human colon with rabbit monoclonal antibody at 1:200 dilution.](http://images.novusbio.com/fullsize/Reg4-Antibody-244-Immunohistochemistry-Paraffin-NBP2-89832-img0001.jpg)
![Western Blot: c-Maf Antibody (JE39-57) [NBP3-32197] - Western blot analysis of c-Maf on different lysates with Rabbit anti-c-Maf antibody (NBP3-32197) at 1/1,000 dilution. Lane 1: A549 cell lysate (10 ug/Lane) Lane 2: Raji cell lysate (10 ug/Lane) Lane 3: Mouse lung tissue lysate (20 ug/Lane) Lane 4: Mouse kidney tissue lysate (20 ug/Lane) Lane 5: Rat spleen tissue lysate (20 ug/Lane) Lane 6: Rat kidney tissue lysate (20 ug/Lane) Predicted band size: 38 kDa Observed band size: 38 kDa Exposure time: 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 (NBP3-32197) 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/nbp3-32197_rabbit-c-maf-mab-je39-57-278202416285292.jpg "Western Blot: c-Maf Antibody (JE39-57) [NBP3-32197] - Western blot analysis of c-Maf on different lysates with Rabbit anti-c-Maf antibody (NBP3-32197) at 1/1,000 dilution. Lane 1: A549 cell lysate (10 ug/Lane) Lane 2: Raji cell lysate (10 ug/Lane) Lane 3: Mouse lung tissue lysate (20 ug/Lane) Lane 4: Mouse kidney tissue lysate (20 ug/Lane) Lane 5: Rat spleen tissue lysate (20 ug/Lane) Lane 6: Rat kidney tissue lysate (20 ug/Lane) Predicted band size: 38 kDa Observed band size: 38 kDa Exposure time: 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 (NBP3-32197) 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.")
![Flow Cytometry: Leptin/OB Antibody (002) [NBP2-89345] - Analysis of Human LEP expression on HeLa cells. The cells were treated, stained with purified anti-Human LEP, 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/Leptin-OB-Antibody-002-Flow-Cytometry-NBP2-89345-img0001.jpg "<b>Biological Strategies Validation. </b>Flow Cytometry: Leptin/OB Antibody (002) [NBP2-89345] - Analysis of Human LEP expression on HeLa cells. The cells were treated, stained with purified anti-Human LEP, 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.")
![<b>Biological Strategies Validation. </b>Immunocytochemistry/Immunofluorescence: Leptin/OB Antibody (002) [NBP2-89345] - Staining of LEP in Hela cells. Cells were fixed with 4% PFA, permeabilzed with 0.1% Triton X-100 in PBS,blocked with 10% serum, and incubated with NBP2-89345 (dilution ratio 1:60) at 4c overnight. Then cells were stained with the Alexa Fluor(R)594-conjugated Goat Anti-rabbit IgG secondary antibody (red). Positive staining was localized to Cytoplasm .](http://images.novusbio.com/fullsize/nbp2-89345_rabbit-monoclonal-leptin-ob-antibody-002-23520251129371.png)
![Flow Cytometry: Fas/TNFRSF6/CD95 Antibody (EOS9.1) - Low Endotoxin, Azide and BSA Free [NBP3-09092] - Separation of anti-CD95 (EOS9.1) antibody stimulated CEM cells (24 hours, 1 ug/ml, red-filled) from nonstimulated CEM cells (black-dashed) in flow cytometry analysis CEM cell suspension stained using ApoFlowEx kit (ED7044).](http://images.novusbio.com/fullsize/Fas-TNFRSF6-CD95-Antibody-EOS9-1-Low-Endotoxin-Azide-and-BSA-Free-Flow-Cytometry-NBP3-09092-img0002.jpg "Flow Cytometry: Fas/TNFRSF6/CD95 Antibody (EOS9.1) - Low Endotoxin, Azide and BSA Free [NBP3-09092] - Separation of anti-CD95 (EOS9.1) antibody stimulated CEM cells (24 hours, 1 ug/ml, red-filled) from nonstimulated CEM cells (black-dashed) in flow cytometry analysis CEM cell suspension stained using ApoFlowEx kit (ED7044).")
![Flow Cytometry: Fas/TNFRSF6/CD95 Antibody (EOS9.1) - Low Endotoxin, Azide and BSA Free [NBP3-09092] - Separation of anti-CD95 (EOS9.1) antibody stimulated Jurkat cells (24 hours, 4 ug/ml, red-filled) from nonstimulated Jurkat cells (black-dashed) in flow cytometry analysis of Jurkat cellular suspension stained using ApoFlowEx kit (ED7044).](http://images.novusbio.com/fullsize/Fas-TNFRSF6-CD95-Antibody-EOS9-1-Low-Endotoxin-Azide-and-BSA-Free-Flow-Cytometry-NBP3-09092-img0001.jpg)
![Western Blot: JNK2 Antibody (004) [NBP2-89620] - Lane A: HepG2 Whole Cell Lysate Lane B: A549 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:48 kDaObserved band size:54 kDa (We are unsure as to the identity of these extra bands.)](http://images.novusbio.com/fullsize/JNK2-Antibody-004-Western-Blot-NBP2-89620-img0003.jpg "Western Blot: JNK2 Antibody (004) [NBP2-89620] - Lane A: HepG2 Whole Cell Lysate Lane B: A549 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:48 kDaObserved band size:54 kDa (We are unsure as to the identity of these extra bands.)")
![Immunoprecipitation: JNK2 Antibody (004) [NBP2-89620] - Lane A:0.5 mg Jurkat Whole Cell Lysate Lane B:0.5 mg A549 Whole Cell Lysate0.5 uL anti-MAPK9 rabbit monoclonal antibody and 15 ul of 50 % Protein G agarose. Primary antibody: Anti-MAPK9 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: 44 kDa Observed band size: 44 kDa](http://images.novusbio.com/fullsize/JNK2-Antibody-004-Immunoprecipitation-NBP2-89620-img0002.jpg)
![Flow Cytometry: CD133 Antibody (W6B3C1) [NBP3-09159] - Analysis (surface staining) of human peripheral whole blood showing CD133 positive stem cells (blue) and lymphocytes (red) stained using anti-CD133 (293C3) purified, GAM-FITC.](http://images.novusbio.com/fullsize/CD133-Antibody-W6B3C1-Flow-Cytometry-NBP3-09159-img0001.jpg "Flow Cytometry: CD133 Antibody (W6B3C1) [NBP3-09159] - Analysis (surface staining) of human peripheral whole blood showing CD133 positive stem cells (blue) and lymphocytes (red) stained using anti-CD133 (293C3) purified, GAM-FITC.")
![Western Blot: IKK beta Antibody (JE32-81) [NBP3-32463] - Western blot analysis of IKK beta on different lysates with Rabbit anti-IKK beta antibody (NBP3-32463) at 1/1,000 dilution. Lane 1: K-562 cell lysate Lane 2: HL-60 cell lysate Lane 3: THP-1 cell lysate Lane 4: Jurkat cell lysate Lane 5: HeLa cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 87 kDa Observed band size: 87 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 (NBP3-32463) 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 1/50,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32463_rabbit-ikk-beta-mab-je32-81-27820241631658.jpg "Western Blot: IKK beta Antibody (JE32-81) [NBP3-32463] - Western blot analysis of IKK beta on different lysates with Rabbit anti-IKK beta antibody (NBP3-32463) at 1/1,000 dilution. Lane 1: K-562 cell lysate Lane 2: HL-60 cell lysate Lane 3: THP-1 cell lysate Lane 4: Jurkat cell lysate Lane 5: HeLa cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 87 kDa Observed band size: 87 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 (NBP3-32463) 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 1/50,000 dilution was used for 1 hour at room temperature.")
![Flow Cytometry: IKK beta Antibody (JE32-81) [NBP3-32463] - Flow cytometric analysis of THP-1 cells labeling IKK beta. Cells were fixed and permeabilized. Then stained with the primary antibody (NBP3-32463, 1/50) (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/nbp3-32463_rabbit-ikk-beta-mab-je32-81-29202416372193.jpg)
![Immunohistochemistry-Paraffin: CD27/TNFRSF7 Antibody (618) [NBP2-90425] - Immunochemical staining of mouse CD27/TNFRSF7 in mouse thymus with NBP2-90425 at 1:200 dilution, formalin-fixed paraffin embedded sections.](http://images.novusbio.com/fullsize/nbp2-90425_rabbit-monoclonal-cd27-tnfrsf7-antibody-618-235202511494044.png "Immunohistochemistry-Paraffin: CD27/TNFRSF7 Antibody (618) [NBP2-90425] - Immunochemical staining of mouse CD27/TNFRSF7 in mouse thymus with NBP2-90425 at 1:200 dilution, formalin-fixed paraffin embedded sections.")
![Immunohistochemistry-Paraffin: CD27/TNFRSF7 Antibody (618) [NBP2-90425] - Staining of mouse CD27/TNFRSF7 in mouse spleen with NBP2-90425 at 1:200 dilution.](http://images.novusbio.com/fullsize/nbp2-90425_rabbit-monoclonal-cd27-tnfrsf7-antibody-618-235202511444465.png)
![Western Blot: Insulin Antibody [NBP1-45662] - Analysis using recombinant human Insulin.](http://images.novusbio.com/fullsize/Insulin-Antibody-Western-Blot-NBP1-45662-img0002.jpg "Western Blot: Insulin Antibody [NBP1-45662] - Analysis using recombinant human Insulin.")
![Immunocytochemistry/Immunofluorescence: CD37 Antibody (WR17) [NBP2-81048] - Immunofluorescence staining of fixed Daudi cells with anti-CD37 antibody (WR17) [NBP2-81048]. Immunofluorescence analysis of paraformaldehyde fixed Daudi cells on Shi-fix coverslips, permeabilized with 0.15% Triton and stained with the chimeric rabbit IgG version of WR17 [NBP2-81048] at 10 ug/ml for 1h followed by Alexa Fluor 488 secondary antibody (1 ug/ml), showing membrane staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP2-81048, DAPI, merged channels and an isotype control. The isotype control was stained with an anti-Fluorescein antibody followed by Alexa Fluor 488 secondary antibody.](http://images.novusbio.com/fullsize/CD37-Antibody-WR17-Immunocytochemistry-Immunofluorescence-NBP2-81048-img0001.jpg "Immunocytochemistry/Immunofluorescence: CD37 Antibody (WR17) [NBP2-81048] - Immunofluorescence staining of fixed Daudi cells with anti-CD37 antibody (WR17) [NBP2-81048]. Immunofluorescence analysis of paraformaldehyde fixed Daudi cells on Shi-fix coverslips, permeabilized with 0.15% Triton and stained with the chimeric rabbit IgG version of WR17 [NBP2-81048] at 10 ug/ml for 1h followed by Alexa Fluor 488 secondary antibody (1 ug/ml), showing membrane staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP2-81048, DAPI, merged channels and an isotype control. The isotype control was stained with an anti-Fluorescein antibody followed by Alexa Fluor 488 secondary antibody.")