| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26653-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| IHC-Prediluted | NBP2-48416 | |||
| Azide and BSA Free | NBP3-11581 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26126-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26577-50ul | |||
![Western Blot: Collagen VII Antibody (D5) [NBP3-41723] - Human Serum; Primary Ab: 3ug/ml NBP3-41723; Second Ab: 0.2ug/mL HRP-conjugated Goat Anti-Mouse IgG Polyclonal Antibody](http://images.novusbio.com/fullsize/nbp3-41723_mouse-collagen-vii-mab-d5-141202515123724.jpg "Western Blot: Collagen VII Antibody (D5) [NBP3-41723] - Human Serum; Primary Ab: 3ug/ml NBP3-41723; Second Ab: 0.2ug/mL HRP-conjugated Goat Anti-Mouse IgG Polyclonal Antibody")
![Flow Cytometry: Claudin-4 Antibody (10F4) [NBP3-26653] - Overlay Peak curve showing MCF7 cells stained with Claudin-4 Antibody (10F4) (red line) at 1:100. Then 10% normal goat serum was Incubated to block non-specific protein-protein interactions followed by the antibody (1ug/1*10^6 cells) for 45 min at 4C. The secondary antibody used was FITC-conjugated Goat Anti-Mouse IgG (H+L) at 1/200 dilution for 35 min at 4C. Isotype control antibody (green line) was mouse IgG1 (1ug/1*10^6 cells) used under the same conditions. Acquisition of >10,000 events was performed.](http://images.novusbio.com/fullsize/nbp3-26653_mouse-claudin-4-mab-10f4-282202414312729.jpg "Flow Cytometry: Claudin-4 Antibody (10F4) [NBP3-26653] - Overlay Peak curve showing MCF7 cells stained with Claudin-4 Antibody (10F4) (red line) at 1:100. Then 10% normal goat serum was Incubated to block non-specific protein-protein interactions followed by the antibody (1ug/1*10^6 cells) for 45 min at 4C. The secondary antibody used was FITC-conjugated Goat Anti-Mouse IgG (H+L) at 1/200 dilution for 35 min at 4C. Isotype control antibody (green line) was mouse IgG1 (1ug/1*10^6 cells) used under the same conditions. Acquisition of >10,000 events was performed.")
![Immunohistochemistry: CA125/MUC16 Antibody (10E9) [NBP3-26126] - Image of CA125/MUC16 Antibody (10E9) diluted at 1:100 and staining in paraffin-embedded human endometrial 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/nbp3-26126_rabbit-ca125-muc16-mab-10e9-26220241522428.jpg "Immunohistochemistry: CA125/MUC16 Antibody (10E9) [NBP3-26126] - Image of CA125/MUC16 Antibody (10E9) diluted at 1:100 and staining in paraffin-embedded human endometrial 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: Fibronectin Antibody (1E1) [NBP3-26577] - Image of Fibronectin Antibody (1E1) 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/nbp3-26577_rabbit-fibronectin-mab-1e1-262202415475639.jpg "Immunohistochemistry: Fibronectin Antibody (1E1) [NBP3-26577] - Image of Fibronectin Antibody (1E1) 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.")