| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-09027-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-12062-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Carrier-Free | NBP2-35105-1mg | |||
| Carrier-Free | NBP2-35105-500ug | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26498-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26431-50ul | |||
![Flow Cytometry: IL-16 Antibody (14.1) - Chimeric [NBP3-09027] - Human peripheral blood leukocytes were stimulated with PMA and Ionomycin in presence of Monensin for 4 hours. The cells were fixed using 2% PFA, permeabilized using 0.5% Triton and stained with anti-Fluorescein IgG antibody (4-4-20; isotype control, black line) or the rabbit IgG version of 14.1 (NBP3-09027, pink line) at a dilution of 1:100 for 1h at RT. The blue line shows unstimulated human peripheral blood leukocytes stained with NBP3-09027. After washing, bound antibody was detected using a goat anti-mouse IgG AlexaFluor(R) 488 antibody at a dilution of 1:1000 and cells were analyzed using a FACSCanto flow-cytometer.](http://images.novusbio.com/fullsize/IL-16-Antibody-14-1-Chimeric-Flow-Cytometry-NBP3-09027-img0001.jpg "Flow Cytometry: IL-16 Antibody (14.1) - Chimeric [NBP3-09027] - Human peripheral blood leukocytes were stimulated with PMA and Ionomycin in presence of Monensin for 4 hours. The cells were fixed using 2% PFA, permeabilized using 0.5% Triton and stained with anti-Fluorescein IgG antibody (4-4-20; isotype control, black line) or the rabbit IgG version of 14.1 (NBP3-09027, pink line) at a dilution of 1:100 for 1h at RT. The blue line shows unstimulated human peripheral blood leukocytes stained with NBP3-09027. After washing, bound antibody was detected using a goat anti-mouse IgG AlexaFluor(R) 488 antibody at a dilution of 1:1000 and cells were analyzed using a FACSCanto flow-cytometer.")
![Immunocytochemistry/Immunofluorescence: TLR2 Antibody (TL2.1) - Chimeric [NBP3-12062] - Immunofluorescence analysis of paraformaldehyde fixed K562 cells on Shi-fix(TM) coverslips stained with the chimeric rabbit IgG version of TL2.1 (NBP3-12062) at 10 ug/ml for 1h followed by Alexa Fluor(R) 488 secondary antibody (2 ug/ml), showing membrane staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP3-12062, DAPI, merged channels and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor(R) 488 secondary antibody.](http://images.novusbio.com/fullsize/TLR2-Antibody-TL2-1-Chimeric-Immunocytochemistry-Immunofluorescence-NBP3-12062-img0001.jpg "Immunocytochemistry/Immunofluorescence: TLR2 Antibody (TL2.1) - Chimeric [NBP3-12062] - Immunofluorescence analysis of paraformaldehyde fixed K562 cells on Shi-fix(TM) coverslips stained with the chimeric rabbit IgG version of TL2.1 (NBP3-12062) at 10 ug/ml for 1h followed by Alexa Fluor(R) 488 secondary antibody (2 ug/ml), showing membrane staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP3-12062, DAPI, merged channels and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor(R) 488 secondary antibody.")
![SDS-Page: Mouse IL-1ra/IL-1F3/IL1RN Protein [NBP2-35105]](http://images.novusbio.com/fullsize/Mouse-IL-1ra-IL-1F3-IL1RN-Protein-SDS-Page-NBP2-35105-img0001.jpg "SDS-Page: Mouse IL-1ra/IL-1F3/IL1RN Protein [NBP2-35105]")
![Immunohistochemistry-Paraffin: CD8 Antibody (C8/1779R) - Azide and BSA Free [NBP2-54595] - CD8 alpha Antibody (C8/1779R) [NBP2-54595] - Formalin-fixed, paraffin-embedded human Lymphoma stained with CD8 Antibody (C8/1779R).](http://images.novusbio.com/fullsize/CD8-alpha-Antibody-C8-1779R-Immunohistochemistry-Paraffin-NBP2-54595-img0002.jpg "Immunohistochemistry-Paraffin: CD8 Antibody (C8/1779R) - Azide and BSA Free [NBP2-54595] - CD8 alpha Antibody (C8/1779R) [NBP2-54595] - Formalin-fixed, paraffin-embedded human Lymphoma stained with CD8 Antibody (C8/1779R).")
![Western Blot: Adenosine A1R Antibody (10D12) [NBP3-15218] - Positive WB detected in: A549 whole cell lysate, 293 whole cell lysate, U87 whole cell lysate. All lanes: Adenosine A1R antibody at 1:2000. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 37, 14 KDa. Observed band size: 37 KDa.](http://images.novusbio.com/fullsize/Adenosine-A1R-Antibody-10D12-Western-Blot-NBP3-15218-img0002.jpg "Western Blot: Adenosine A1R Antibody (10D12) [NBP3-15218] - Positive WB detected in: A549 whole cell lysate, 293 whole cell lysate, U87 whole cell lysate. All lanes: Adenosine A1R antibody at 1:2000. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 37, 14 KDa. Observed band size: 37 KDa.")
![Immunohistochemistry: Adenosine A1R Antibody (10D12) [NBP3-15218] - IHC image of Adenosine A1R antibody diluted at 1:100 and staining in paraffin-embedded human brain tissue. 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 30 minutes 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/Adenosine-A1R-Antibody-10D12-Immunohistochemistry-NBP3-15218-img0001.jpg)
![Western Blot: GBP5 Antibody [NBP1-32520] - Untreated (-) and treated (+) Raw264.7 whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with GBP5 antibody [N1N3] diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.](http://images.novusbio.com/fullsize/GBP5-Antibody-Western-Blot-NBP1-32520-img0003.jpg "Western Blot: GBP5 Antibody [NBP1-32520] - Untreated (-) and treated (+) Raw264.7 whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with GBP5 antibody [N1N3] diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.")
![<b>Biological Strategies Validation. </b>Western Blot: GBP5 Antibody [NBP1-32520] - Untreated (-) and treated (+) THP-1 whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with GBP5 antibody [N1N3] diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.](http://images.novusbio.com/fullsize/GBP5-Antibody-Western-Blot-NBP1-32520-img0002.jpg)
![Immunohistochemistry: ATF2 Antibody (3D12) [NBP3-26498] - Image of ATF2 Antibody (3D12) diluted at 1:115.5 and staining in paraffin-embedded human prostate 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/nbp3-26498_rabbit-atf2-mab-3d12-262202414471538.jpg "Immunohistochemistry: ATF2 Antibody (3D12) [NBP3-26498] - Image of ATF2 Antibody (3D12) diluted at 1:115.5 and staining in paraffin-embedded human prostate 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: ATF2 Antibody (3D12) [NBP3-26498] - Positive Western Blot detected in: K562 whole cell lysate, 293T whole cell lysate. All lanes: ATF2 Antibody at 1.2ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 55, 36, 24, 49, 53, 14, 25, 16 KDa Observed band size: 70 KDa](http://images.novusbio.com/fullsize/nbp3-26498_rabbit-atf2-mab-3d12-2822024115253.jpg)
![Western Blot: ATF2 [p Thr71] Antibody (4F2) [NBP3-26431] - Positive Western Blot detected in 293 whole cell lysate, A549 whole cell lysate, HepG2 whole cell lysate (treated with Calyculin A or EGF). All lanes: ATF2 [p Thr71] Antibody at 1.015ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 70 KDa Observed band size: 70 KDa](http://images.novusbio.com/fullsize/nbp3-26431_rabbit-atf2-p-thr-71-mab-4f2-28220241152514.jpg "Western Blot: ATF2 [p Thr71] Antibody (4F2) [NBP3-26431] - Positive Western Blot detected in 293 whole cell lysate, A549 whole cell lysate, HepG2 whole cell lysate (treated with Calyculin A or EGF). All lanes: ATF2 [p Thr71] Antibody at 1.015ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 70 KDa Observed band size: 70 KDa")
![Immunocytochemistry/Immunofluorescence: ATF2 [p Thr71] Antibody (4F2) [NBP3-26431] - Staining of A549 cells(treated with 100mM EGF for 20min) with ATF2 [p Thr71] Antibody (4F2) at 1:63, 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/nbp3-26431_rabbit-atf2-p-thr-71-mab-4f2-28220241323615.jpg)