| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-54412-100ug | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26691-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26613-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26338-50ul | |||
![Western Blot: CXCL7/NAP-2 Antibody (15#) [NBP3-41148] - Sample: Lane1: Human Serum; Lane2: Human Leukocyte cell lysate Primary Ab: 3ug/ml NBP3-41148; Second Ab: 0.2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody](http://images.novusbio.com/fullsize/nbp3-41148_mouse-cxcl7-nap-2-mab-15-612202421283822.jpg "Western Blot: CXCL7/NAP-2 Antibody (15#) [NBP3-41148] - Sample: Lane1: Human Serum; Lane2: Human Leukocyte cell lysate Primary Ab: 3ug/ml NBP3-41148; Second Ab: 0.2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody")
![ELISA: Human CXCL7/NAP-2 ELISA Kit (Colorimetric) [NBP2-59965]](http://images.novusbio.com/fullsize/Human-CXCL7-NAP-2-ELISA-Kit-Colorimetric-ELISA-NBP2-59965-img0001.jpg "ELISA: Human CXCL7/NAP-2 ELISA Kit (Colorimetric) [NBP2-59965]")
![Human CXCL7/NAP-2 ELISA Kit (Colorimetric) [NBP2-59965] - Standard Curve Reference](http://images.novusbio.com/fullsize/nbp2-59965_human-cxcl7-nap-2-elisa-kit-colorimetric-3120248485440.png)
![Immunocytochemistry/Immunofluorescence: CXCR4 Antibody (2F10) [NBP3-15137] - Immunofluorescence staining of Hela Cells with CXCR4 antibody at 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeated by 0.2% TritonX-100, and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. Nuclear DNA was labeled in blue with DAPI. The secondary antibody was FITC-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/CXCR4-Antibody-2F10-Immunocytochemistry-Immunofluorescence-NBP3-15137-img0001.jpg "Immunocytochemistry/Immunofluorescence: CXCR4 Antibody (2F10) [NBP3-15137] - Immunofluorescence staining of Hela Cells with CXCR4 antibody at 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeated by 0.2% TritonX-100, and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. Nuclear DNA was labeled in blue with DAPI. The secondary antibody was FITC-conjugated Goat Anti-Rabbit IgG (H+L).")
![ELISA: Mouse TGF-beta 1 ELISA Kit [NBP1-92671]](http://images.novusbio.com/fullsize/Mouse-TGF-beta-1-ELISA-Kit-ELISA-NBP1-92671-img0001.jpg "ELISA: Mouse TGF-beta 1 ELISA Kit [NBP1-92671]")
![Immunohistochemistry: CCR2 Antibody (6A1) [NBP3-26691] - Image of CCR2 Antibody (6A1) diluted at 1:100 and staining in paraffin-embedded human tonsil 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 Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26691_rabbit-ccr2-mab-6a1-2622024151061.jpg "Immunohistochemistry: CCR2 Antibody (6A1) [NBP3-26691] - Image of CCR2 Antibody (6A1) diluted at 1:100 and staining in paraffin-embedded human tonsil 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 Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.")
![Immunohistochemistry: DPPIV/CD26 Antibody (6G7) [NBP3-26613] - Image of DPPIV/CD26 Antibody (6G7) diluted at 1:100 and staining in paraffin-embedded human prostate 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 Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26613_rabbit-dppiv-cd26-mab-6g7-27220248573311.jpg "Immunohistochemistry: DPPIV/CD26 Antibody (6G7) [NBP3-26613] - Image of DPPIV/CD26 Antibody (6G7) diluted at 1:100 and staining in paraffin-embedded human prostate 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 Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.")
![Immunohistochemistry: S100A9 Antibody (2E9) [NBP3-26338] - Image of S100A9 Antibody (2E9) diluted at 1:100 and staining in paraffin-embedded human breast 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 Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26338_rabbit-s100a9-mab-2e9-26220241525338.jpg "Immunohistochemistry: S100A9 Antibody (2E9) [NBP3-26338] - Image of S100A9 Antibody (2E9) diluted at 1:100 and staining in paraffin-embedded human breast 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 Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.")