| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-08922 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Carrier-Free | NBP2-35109-1mg | |||
| Carrier-Free | NBP2-35109-100ug | |||
| Carrier-Free | NBP2-35109-500ug | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-99921-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26159-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26468-50ul | |||
![Western Blot: MMP-2 Antibody (3Q7R10) [NBP3-15653] - Western blot analysis of extracts of various cell lines, using MMP-2 antibody (NBP3-15653) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 90s.](http://images.novusbio.com/fullsize/MMP-2-Antibody-3Q7R10-Western-Blot-NBP3-15653-img0001.jpg "Western Blot: MMP-2 Antibody (3Q7R10) [NBP3-15653] - Western blot analysis of extracts of various cell lines, using MMP-2 antibody (NBP3-15653) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 90s.")
![Western Blot: LYVE-1 Antibody (4G7C3) [NBP3-16385] - Western blot analysis of extracts of various cell lines, using LYVE-1 Rabbit mAb (NBP3-16385) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 60s.](http://images.novusbio.com/fullsize/LYVE-1-Antibody-4G7C3-Western-Blot-NBP3-16385-img0001.jpg "Western Blot: LYVE-1 Antibody (4G7C3) [NBP3-16385] - Western blot analysis of extracts of various cell lines, using LYVE-1 Rabbit mAb (NBP3-16385) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 60s.")
![SDS-Page: Mouse IL-1 beta/IL-1F2 Protein [NBP2-35109]](http://images.novusbio.com/fullsize/Mouse-IL-1-beta-IL-1F2-Protein-SDS-Page-NBP2-35109-img0001.jpg "SDS-Page: Mouse IL-1 beta/IL-1F2 Protein [NBP2-35109]")
![Immunohistochemistry-Paraffin: Carbonic Anhydrase IX/CA9 Antibody (09) - Azide and BSA Free [NBP3-26103] - Immunochemical staining of human Carbonic Anhydrase IX/CA9 in human stomach with mouse monoclonal antibody (1:200, formalin-fixed paraffin embedded sections).](http://images.novusbio.com/fullsize/nbp3-26103_mouse-carbonic-anhydrase-ix-ca9-mab-09-azide-bsa-free-12620241540466.png "Immunohistochemistry-Paraffin: Carbonic Anhydrase IX/CA9 Antibody (09) - Azide and BSA Free [NBP3-26103] - Immunochemical staining of human Carbonic Anhydrase IX/CA9 in human stomach with mouse monoclonal antibody (1:200, formalin-fixed paraffin embedded sections).")
![Immunohistochemistry-Paraffin: Carbonic Anhydrase IX/CA9 Antibody (09) - Azide and BSA Free [NBP3-26103] - Immunochemical staining of human Carbonic Anhydrase IX/CA9 in human renal carcinoma with mouse monoclonal antibody (1:200, formalin-fixed paraffin embedded sections).](http://images.novusbio.com/fullsize/nbp3-26103_mouse-carbonic-anhydrase-ix-ca9-mab-09-azide-bsa-free-13620241428460.png)
![Western Blot: HRAS Antibody [NBP2-99921] - Anti-HRAS rabbit polyclonal antibody at 1:500 dilution. Lane A: MCF7 Whole Cell Lysate. Lane B: HepG2 Whole Cell Lysate. Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG H&L (Dylight 800) at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size: 21 kDa. Observed band size: 21 kDa](http://images.novusbio.com/fullsize/HRAS-Antibody-Western-Blot-NBP2-99921-img0004.jpg "Western Blot: HRAS Antibody [NBP2-99921] - Anti-HRAS rabbit polyclonal antibody at 1:500 dilution. Lane A: MCF7 Whole Cell Lysate. Lane B: HepG2 Whole Cell Lysate. Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG H&L (Dylight 800) at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size: 21 kDa. Observed band size: 21 kDa")
![Immunoprecipitation: HRAS Antibody [NBP2-99921] - HRAS was immunoprecipitated using: Lane A: 0.5 mg HepG2 Whole Cell Lysate. Lane B: 0.5 mg MCF-7 Whole Cell Lysate 2 ul anti-HRAS rabbit polyclonal antibody and 15 ul of 50 % Protein G agarose. Primary antibody: Anti-HRAS rabbit polyclonal antibody, at 1:200 dilution. Secondary antibody: Dylight 800-labeled antibody to rabbit IgG (H+L), at 1:5000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size: 21 kDa. Observed band size: 21 kDa](http://images.novusbio.com/fullsize/HRAS-Antibody-Immunoprecipitation-NBP2-99921-img0003.jpg)
![Immunocytochemistry/Immunofluorescence: LYVE-1 Antibody (11C11) [NBP3-26159] - Staining of HepG2 with LYVE-1 Antibody (11C11) at 1:25, counter-stained with DAPI. The cells were fixed in 4% formaldehyde and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 505-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26159_rabbit-lyve-1-mab-11c11-28220241249369.jpg "Immunocytochemistry/Immunofluorescence: LYVE-1 Antibody (11C11) [NBP3-26159] - Staining of HepG2 with LYVE-1 Antibody (11C11) at 1:25, counter-stained with DAPI. The cells were fixed in 4% formaldehyde and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 505-conjugated Goat Anti-Rabbit IgG (H+L).")
![Flow Cytometry: LYVE-1 Antibody (11C11) [NBP3-26159] - Overlay Peak curve showing HepG2 cells stained with LYVE-1 Antibody (11C11) (red line) at 1:50. The cells were fixed in 4% formaldehyde and permeated by 0.2% Triton X-100. Then 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10^6 cells) for 45min at 4C. The secondary antibody used was FITC-conjugated Goat Anti-rabbit IgG (H+L) at 1:200 dilution for 35min at 4C. Control antibody (green line) was rabbit IgG (1ug/1*10^6 cells) used under the same conditions. Acquisition of >10,000 events was performed.](http://images.novusbio.com/fullsize/nbp3-26159_rabbit-lyve-1-mab-11c11-28220241418361.jpg)
![Immunohistochemistry: Carbonic Anhydrase IX/CA9 Antibody (4F12) [NBP3-26468] - Image of Carbonic Anhydrase IX/CA9 Antibody (4F12) diluted at 1:118 and staining in paraffin-embedded human gastric cancer 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/nbp3-26468_rabbit-carbonic-anhydrase-ix-ca9-mab-4f12-262202414471598.jpg "Immunohistochemistry: Carbonic Anhydrase IX/CA9 Antibody (4F12) [NBP3-26468] - Image of Carbonic Anhydrase IX/CA9 Antibody (4F12) diluted at 1:118 and staining in paraffin-embedded human gastric cancer 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.")
![Immunohistochemistry: Carbonic Anhydrase IX/CA9 Antibody (4F12) [NBP3-26468] - Image of Carbonic Anhydrase IX/CA9 Antibody (4F12) diluted at 1:118 and staining in paraffin-embedded human gastric cancer 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/nbp3-26468_rabbit-carbonic-anhydrase-ix-ca9-mab-4f12-262202414471569.jpg)