| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-11968-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-09052-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-81048-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-09016-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-11399 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-11439 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26650-50ul | |||
![Flow Cytometry: HLA-E Antibody (3D12) [NBP2-76812] - Separation of human lymphocytes (red-filled) from blood debris (black-dashed) in flow cytometry analysis (surface staining) of human peripheral whole blood stained using HLA-E Antibody (concentration in sample 4 ug/ml) GAM APC.](http://images.novusbio.com/fullsize/HLA-E-Antibody-3D12-Flow-Cytometry-NBP2-76812-img0002.jpg "Flow Cytometry: HLA-E Antibody (3D12) [NBP2-76812] - Separation of human lymphocytes (red-filled) from blood debris (black-dashed) in flow cytometry analysis (surface staining) of human peripheral whole blood stained using HLA-E Antibody (concentration in sample 4 ug/ml) GAM APC.")
![Flow Cytometry: HLA-E Antibody (3D12) [NBP2-76812] - Flow cytometry surface staining pattern of human peripheral blood stained using HLA-E Antibody (concentration in sample 4 ug/ml) GAM APC.](http://images.novusbio.com/fullsize/HLA-E-Antibody-3D12-Flow-Cytometry-NBP2-76812-img0001.jpg)
![Immunocytochemistry/Immunofluorescence: CD37 Antibody (G28-1) - Chimeric [NBP3-09052] - Immunofluorescence analysis of paraformaldehyde fixed Daudi cells on Shi-fix(TM) coverslips stained with the chimeric rabbit IgG version of G28-1 (NBP3-09052) 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 NBP3-09052, 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/CD37-Antibody-G28-1-Chimeric-Immunocytochemistry-Immunofluorescence-NBP3-09052-img0001.jpg "Immunocytochemistry/Immunofluorescence: CD37 Antibody (G28-1) - Chimeric [NBP3-09052] - Immunofluorescence analysis of paraformaldehyde fixed Daudi cells on Shi-fix(TM) coverslips stained with the chimeric rabbit IgG version of G28-1 (NBP3-09052) 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 NBP3-09052, 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.")
![Flow Cytometry: CD37 Antibody (G28-1) - Chimeric [NBP3-09052] - Analysis of Daudi cells](http://images.novusbio.com/fullsize/CD37-Antibody-G28-1-Chimeric-Flow-Cytometry-NBP3-09052-img0002.jpg)
![Immunocytochemistry/ Immunofluorescence: HLA G Antibody (mem-G/9) - BSA Free [NBP3-43580] - Immunofluorescence analysis of paraformaldehyde fixed K562 cells on coverslips stained with the chimeric version of this antibody, NBP3-43580 (1:100 dilution) for 1h followed by Alexa Fluor® 488 secondary antibody (1:1000 dilution), showing membrane and cytoplasmic staining. The nuclear stain is DAPI (blue). Panels show, from left-right, top-bottom, NBP3-43580, DAPI, merged channels and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor® 488 secondary antibody.](http://images.novusbio.com/fullsize/nbp3-43580_mouse-hla-g-mab-mem-g-9-azide-and-bsa-free-immunocytochemistry-immunofluorescence-222026033310.png "Immunocytochemistry/ Immunofluorescence: HLA G Antibody (mem-G/9) - BSA Free [NBP3-43580] - Immunofluorescence analysis of paraformaldehyde fixed K562 cells on coverslips stained with the chimeric version of this antibody, NBP3-43580 (1:100 dilution) for 1h followed by Alexa Fluor® 488 secondary antibody (1:1000 dilution), showing membrane and cytoplasmic staining. The nuclear stain is DAPI (blue). Panels show, from left-right, top-bottom, NBP3-43580, DAPI, merged channels and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor® 488 secondary antibody.")
![Immunocytochemistry/Immunofluorescence: CD37 Antibody (WR17) [NBP2-81048] - Immunofluorescence staining of fixed Daudi cells with anti-CD37 antibody (WR17) [NBP2-81048]. Immunofluorescence analysis of paraformaldehyde fixed Daudi cells on Shi-fix coverslips, permeabilized with 0.15% Triton and stained with the chimeric rabbit IgG version of WR17 [NBP2-81048] at 10 ug/ml for 1h followed by Alexa Fluor 488 secondary antibody (1 ug/ml), showing membrane staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP2-81048, DAPI, merged channels and an isotype control. The isotype control was stained with an anti-Fluorescein antibody followed by Alexa Fluor 488 secondary antibody.](http://images.novusbio.com/fullsize/CD37-Antibody-WR17-Immunocytochemistry-Immunofluorescence-NBP2-81048-img0001.jpg "Immunocytochemistry/Immunofluorescence: CD37 Antibody (WR17) [NBP2-81048] - Immunofluorescence staining of fixed Daudi cells with anti-CD37 antibody (WR17) [NBP2-81048]. Immunofluorescence analysis of paraformaldehyde fixed Daudi cells on Shi-fix coverslips, permeabilized with 0.15% Triton and stained with the chimeric rabbit IgG version of WR17 [NBP2-81048] at 10 ug/ml for 1h followed by Alexa Fluor 488 secondary antibody (1 ug/ml), showing membrane staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP2-81048, DAPI, merged channels and an isotype control. The isotype control was stained with an anti-Fluorescein antibody followed by Alexa Fluor 488 secondary antibody.")
![Immunocytochemistry /Immunofluorescence: HLA G Antibody (mem-G/9) - BSA Free [NBP3-43587] - Immunofluorescence analysis of paraformaldehyde fixed K562 cells on Shi-fix coverslips stained with NBP3-43587 (1:100 dilution) for 1h followed by Alexa Fluor 488 secondary antibody (1:1000 dilution), showing membrane and cytoplasmic staining. The nuclear stain is DAPI (blue). Panels show, from left-right, top-bottom, NBP3-43587, DAPI, merged channels and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor 488 secondary antibody.](http://images.novusbio.com/fullsize/nbp3-43587_rabbit-hla-g-mab-mem-g-9-azide-and-bsa-free-74202522113046.png "Immunocytochemistry /Immunofluorescence: HLA G Antibody (mem-G/9) - BSA Free [NBP3-43587] - Immunofluorescence analysis of paraformaldehyde fixed K562 cells on Shi-fix coverslips stained with NBP3-43587 (1:100 dilution) for 1h followed by Alexa Fluor 488 secondary antibody (1:1000 dilution), showing membrane and cytoplasmic staining. The nuclear stain is DAPI (blue). Panels show, from left-right, top-bottom, NBP3-43587, DAPI, merged channels and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor 488 secondary antibody.")
![Immunocytochemistry /Immunofluorescence: MHC Class I Antibody (R1-9.6) - Chimeric - Azide and BSA Free [NBP3-09016] - Immunofluorescence analysis of paraformaldehyde fixed mouse splenocytes immobilized on Shi-fix(TM) cover-slips and stained with NBP3-09016 at 10 ug/ml followed by Alexa Fluor(R) 488 secondary antibody (2 ug/ml), showing membrane staining in a subset of cells. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom: NBP3-09016, DAPI, merged channels and an isotype control. The isotype control was stained with anti-Fluorescein antibody followed by Alexa Fluor(R) 488 secondary antibody.](http://images.novusbio.com/fullsize/nbp3-09016_rabbit-monoclonal-mhc-class-i-antibody-r1-9-6-chimeric-74202522265213.png "Immunocytochemistry /Immunofluorescence: MHC Class I Antibody (R1-9.6) - Chimeric - Azide and BSA Free [NBP3-09016] - Immunofluorescence analysis of paraformaldehyde fixed mouse splenocytes immobilized on Shi-fix(TM) cover-slips and stained with NBP3-09016 at 10 ug/ml followed by Alexa Fluor(R) 488 secondary antibody (2 ug/ml), showing membrane staining in a subset of cells. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom: NBP3-09016, DAPI, merged channels and an isotype control. The isotype control was stained with anti-Fluorescein antibody followed by Alexa Fluor(R) 488 secondary antibody.")
![Immunohistochemistry-Paraffin: HLA A Antibody (SPM417) - IHC-Prediluted [NBP2-48098] - Human Tonsil stained with MHC I Monoclonal Antibody (SPM417).](http://images.novusbio.com/fullsize/HLA-A-Antibody-SPM417-IHC-Prediluted-Immunohistochemistry-Paraffin-NBP2-48098-img0001.jpg "Immunohistochemistry-Paraffin: HLA A Antibody (SPM417) - IHC-Prediluted [NBP2-48098] - Human Tonsil stained with MHC I Monoclonal Antibody (SPM417).")
![Immunohistochemistry: Clusterin/APOJ Antibody (2A1) [NBP3-26650] - Image of Clusterin/APOJ Antibody (2A1) 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/nbp3-26650_rabbit-clusterin-apoj-mab-2a1-262202414471524.jpg "Immunohistochemistry: Clusterin/APOJ Antibody (2A1) [NBP3-26650] - Image of Clusterin/APOJ Antibody (2A1) 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.")
![Immunohistochemistry: Clusterin/APOJ Antibody (2A1) [NBP3-26650] - Image of Clusterin/APOJ Antibody (2A1) 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/nbp3-26650_rabbit-clusterin-apoj-mab-2a1-262202415475621.jpg)