| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-08371 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-72337 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26127-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26126-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-44101 | |||
| BSA Free | NBP2-59024-25ul | |||
![Immunohistochemistry: CA125/MUC16 Antibody (PD01-13) [NBP3-32614] - Immunohistochemical analysis of paraffin-embedded human ovarian serous carcinoma tissue with Rabbit anti-CA125/MUC16 antibody (NBP3-32614) at 1/1,000 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (NBP3-32614) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.](http://images.novusbio.com/fullsize/nbp3-32614_rabbit-ca125-muc16-mab-pd01-13-29820241358558.jpg "Immunohistochemistry: CA125/MUC16 Antibody (PD01-13) [NBP3-32614] - Immunohistochemical analysis of paraffin-embedded human ovarian serous carcinoma tissue with Rabbit anti-CA125/MUC16 antibody (NBP3-32614) at 1/1,000 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (NBP3-32614) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.")
![Immunocytochemistry/ Immunofluorescence: CA125/MUC16 Antibody (PD01-13) [NBP3-32614] - Immunocytochemistry analysis of SKOV-3 cells labeling CA125/MUC16 with Rabbit anti-CA125/MUC16 antibody (NBP3-32614) at 1/50 dilution. Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.05% Triton X-100 in PBS for 20 minutes, and then blocked with 2% negative goat serum for 30 minutes at room temperature. Cells were then incubated with Rabbit anti-CA125/MUC16 antibody (NBP3-32614) at 1/50 dilution in 2% negative goat serum overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. Nuclear DNA was labelled in blue with DAPI. Beta tubulin (red) was stained at 1/200 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594) was used as the secondary antibody at 1/1,000 dilution.](http://images.novusbio.com/fullsize/nbp3-32614_rabbit-ca125-muc16-mab-pd01-13-29202410484871.jpg)
![Immunohistochemistry-Paraffin: CA125/MUC16 Antibody (OCA125/2349R) [NBP3-07573] - Formalin-fixed, paraffin-embedded human Endometrial Carcinoma stained with CA125/MUC16 Rabbit Recombinant Monoclonal Antibody (OCA125/2349R).](http://images.novusbio.com/fullsize/CA125-MUC16-Antibody-OCA125-2349R-Immunohistochemistry-Paraffin-NBP3-07573-img0002.jpg "Immunohistochemistry-Paraffin: CA125/MUC16 Antibody (OCA125/2349R) [NBP3-07573] - Formalin-fixed, paraffin-embedded human Endometrial Carcinoma stained with CA125/MUC16 Rabbit Recombinant Monoclonal Antibody (OCA125/2349R).")
![Immunohistochemistry-Paraffin: CA125/MUC16 Antibody (OCA125/2349R) [NBP3-07573] - Formalin-fixed, paraffin-embedded human Ovarian Carcinoma stained with CA125/MUC16 Rabbit Recombinant Monoclonal Antibody (OCA125/2349R).](http://images.novusbio.com/fullsize/CA125-MUC16-Antibody-OCA125-2349R-Immunohistochemistry-Paraffin-NBP3-07573-img0001.jpg)
![Western Blot: CA125/MUC16 Antibody (3C6) [NBP2-46052] - Analysis of HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY MUC16 (SC200446, Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted.](http://images.novusbio.com/fullsize/CA125-MUC16-Antibody-3C6-Western-Blot-NBP2-46052-img0001.jpg "Western Blot: CA125/MUC16 Antibody (3C6) [NBP2-46052] - Analysis of HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY MUC16 (SC200446, Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted.")
![Immunohistochemistry: CA125/MUC16 Antibody (10F10) [NBP3-26127] - Image of CA125/MUC16 Antibody (10F10) 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/nbp3-26127_rabbit-ca125-muc16-mab-10f10-262202415253328.jpg "Immunohistochemistry: CA125/MUC16 Antibody (10F10) [NBP3-26127] - Image of CA125/MUC16 Antibody (10F10) 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: 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.")