| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-09016-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-09028-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-12052-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-09042-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-12043-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-11514 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-11399 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26650-50ul | |||
![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.")
![Flow Cytometry: Fc epsilon RI Antibody (IE7) - Chimeric [NBP3-12052] - U937 cells were stained with anti-Fluorescein IgG antibody (4-4-20; isotype control, black line) or the rabbit IgG version of IE7 (NBP3-12052, blue line) at a dilution of 1:100 for 1h at RT. After washing, bound antibody was detected using a goat anti-rabbit IgG AlexaFluor(R) 488 antibody at a dilution of 1:1000 and cells analyzed using a FACSCanto flow-cytometer.](http://images.novusbio.com/fullsize/Fc-epsilon-RI-Antibody-IE7-Chimeric-Flow-Cytometry-NBP3-12052-img0002.jpg "Flow Cytometry: Fc epsilon RI Antibody (IE7) - Chimeric [NBP3-12052] - U937 cells were stained with anti-Fluorescein IgG antibody (4-4-20; isotype control, black line) or the rabbit IgG version of IE7 (NBP3-12052, blue line) at a dilution of 1:100 for 1h at RT. After washing, bound antibody was detected using a goat anti-rabbit IgG AlexaFluor(R) 488 antibody at a dilution of 1:1000 and cells analyzed using a FACSCanto flow-cytometer.")
![Immunocytochemistry /Immunofluorescence: Fc epsilon RI Antibody (IE7) - Chimeric - Azide and BSA Free [NBP3-12052] - Immunofluorescence analysis of paraformaldehyde fixed U937 cells immobilized on Shi-fix(TM) cover-slips and stained with NBP3-12052 at 10 ug/ml 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 NBP3-12052, DAPI, merged channels and an isotype control. The isotype control was stained with anti-Fluorescein antibody (NBP2-52638) followed by Alexa Fluor(R) 488 secondary antibody.](http://images.novusbio.com/fullsize/nbp3-12052_rabbit-monoclonal-fc-epsilon-ri-antibody-ie7-chimeric-74202522265214.png)
![Immunocytochemistry/Immunofluorescence: RHD Antibody (D7C2) - Chimeric [NBP3-09042] - Immunofluorescence analysis of paraformaldehyde fixed K562 cells on Shi-fix(TM) coverslips stained with the chimeric rabbit IgG version of D7C2 (NBP3-09042) 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 NBP3-09042, 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/RHD-Antibody-D7C2-Chimeric-Immunocytochemistry-Immunofluorescence-NBP3-09042-img0001.jpg "Immunocytochemistry/Immunofluorescence: RHD Antibody (D7C2) - Chimeric [NBP3-09042] - Immunofluorescence analysis of paraformaldehyde fixed K562 cells on Shi-fix(TM) coverslips stained with the chimeric rabbit IgG version of D7C2 (NBP3-09042) 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 NBP3-09042, 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: RHD Antibody (D7C2) - Chimeric - Azide and BSA Free [NBP3-09042] - Paraformaldehyde fixed K562 cells were stained with anti-unknown specificity antibody (isotype control, black line) or NBP3-09042 (blue line) at a dilution of 1:100 for 1h at RT. After washing, the bound antibody was detected using a goat anti-rabbit IgG AlexaFluor 488 antibody at a dilution of 1:1000 and cells analyzed using a FACSCanto flow-cytometer.](http://images.novusbio.com/fullsize/nbp3-09042_rabbit-monoclonal-rhd-antibody-d7c2-chimeric-74202522113048.png)
![Immunocytochemistry/Immunofluorescence: MS4A4A Antibody (5C12) - Chimeric [NBP3-12043] - Immunofluorescence analysis of paraformaldehyde fixed K562 cells on Shi-fix(TM) coverslips stained with the chimeric rabbit IgG version of 5C12 (NBP3-12043) 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 NBP3-12043, 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/MS4A4A-Antibody-5C12-Chimeric-Immunocytochemistry-Immunofluorescence-NBP3-12043-img0001.jpg "Immunocytochemistry/Immunofluorescence: MS4A4A Antibody (5C12) - Chimeric [NBP3-12043] - Immunofluorescence analysis of paraformaldehyde fixed K562 cells on Shi-fix(TM) coverslips stained with the chimeric rabbit IgG version of 5C12 (NBP3-12043) 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 NBP3-12043, 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.")
![Immunocytochemistry /Immunofluorescence: TCR beta Antibody (IARC307) - Chimeric - BSA Free [NBP3-43545] - Immunofluorescence analysis of paraformaldehyde fixed Jurkat cells on Shi-fix coverslips stained with NBP3-43545 at 10 ug/ml for 1h followed by Alexa Fluor 488 secondary antibody (2 ug/ml), showing membrane staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP3-43545, 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/nbp3-43545_rabbit-tcr-beta-mab-iarc307-chimeric-azide-bsa-free-74202522113029.png "Immunocytochemistry /Immunofluorescence: TCR beta Antibody (IARC307) - Chimeric - BSA Free [NBP3-43545] - Immunofluorescence analysis of paraformaldehyde fixed Jurkat cells on Shi-fix coverslips stained with NBP3-43545 at 10 ug/ml for 1h followed by Alexa Fluor 488 secondary antibody (2 ug/ml), showing membrane staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP3-43545, DAPI, merged channels and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor 488 secondary antibody.")
![Flow Cytometry: TCR beta Antibody (IARC307) - Chimeric - BSA Free [NBP3-43545] - Paraformaldehyde fixed Jurkat cells permeabilized with 0.5% Triton were stained with anti-unknown specificity antibody (isotype control, black line) or NBP3-43545 (blue line) at a dilution of 1:100 for 1h at RT. After washing, the bound antibody was detected using a goat anti-rabbit IgG AlexaFluor 488 antibody at a dilution of 1:1000 and cells analyzed using a FACSCanto flow-cytometer.](http://images.novusbio.com/fullsize/nbp3-43545_rabbit-tcr-beta-mab-iarc307-chimeric-azide-bsa-free-74202522141238.png)
![Immunohistochemistry-Paraffin: SSEA-1 Antibody (FUT4/815 + BRA-4F1) - IHC-Prediluted [NBP2-48448] - Formalin-fixed, paraffin-embedded human Hodgkin's lymphoma stained with CD15 Mouse Monoclonal Antibody (FUT4/815 + BRA-4F1).](http://images.novusbio.com/fullsize/SSEA-1-Antibody-FUT4-815-+-BRA-4F1-IHC-Prediluted-Immunohistochemistry-Paraffin-NBP2-48448-img0001.jpg "Immunohistochemistry-Paraffin: SSEA-1 Antibody (FUT4/815 + BRA-4F1) - IHC-Prediluted [NBP2-48448] - Formalin-fixed, paraffin-embedded human Hodgkin's lymphoma stained with CD15 Mouse Monoclonal Antibody (FUT4/815 + BRA-4F1).")
![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)