| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-81272SS | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-20148-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-11994-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26312-50ul | |||
![Immunocytochemistry/Immunofluorescence: NFkB p100/p52 Antibody (SAIC-26C-15) [NBP2-81272] - Immunofluorescence staining of fixed HeLa cells with NFkB p100/p52 Antibody (SAIC-26C-15) [NBP2-81272]. Immunofluorescence analysis of paraformaldehyde fixed HeLa cells on Shi-fix coverslips, permeabilized with 0.15% Triton and stained with the chimeric rabbit IgG version of SAIC-26C-15 [NBP2-81272] at 10 ug/ml for 1h followed by Alexa Fluor 488 secondary antibody (1 ug/ml), showing cytoplasmic staining, most likely in the ER. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP2-81272, 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/NFkB-p100-p52-Antibody-SAIC-26C-15-Immunocytochemistry-Immunofluorescence-NBP2-81272-img0001.jpg "Immunocytochemistry/Immunofluorescence: NFkB p100/p52 Antibody (SAIC-26C-15) [NBP2-81272] - Immunofluorescence staining of fixed HeLa cells with NFkB p100/p52 Antibody (SAIC-26C-15) [NBP2-81272]. Immunofluorescence analysis of paraformaldehyde fixed HeLa cells on Shi-fix coverslips, permeabilized with 0.15% Triton and stained with the chimeric rabbit IgG version of SAIC-26C-15 [NBP2-81272] at 10 ug/ml for 1h followed by Alexa Fluor 488 secondary antibody (1 ug/ml), showing cytoplasmic staining, most likely in the ER. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP2-81272, DAPI, merged channels and an isotype control. The isotype control was stained with an anti-Fluorescein antibody followed by Alexa Fluor 488 secondary antibody.")
![Flow Cytometry: NMDAR2B Antibody (17) - Chimeric - BSA Free [NBP3-43544] - Paraformaldehyde fixed C6 cells permeabilized with 0.5% Triton were stained with anti-unknown specificity antibody (isotype control, black line) or NBP3-43544 (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/nbp3-43544_rabbit-nmdar2b-mab-17-chimeric-azide-and-bsa-free-7420252226524.png "Flow Cytometry: NMDAR2B Antibody (17) - Chimeric - BSA Free [NBP3-43544] - Paraformaldehyde fixed C6 cells permeabilized with 0.5% Triton were stained with anti-unknown specificity antibody (isotype control, black line) or NBP3-43544 (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.")
![Immunocytochemistry /Immunofluorescence: NMDAR2B Antibody (17) - Chimeric - BSA Free [NBP3-43544] - Immunofluorescence analysis of paraformaldehyde fixed C6 cells stained with NBP3-43544 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 NBP3-43544, 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/nbp3-43544_rabbit-nmdar2b-mab-17-chimeric-azide-and-bsa-free-74202522141223.png)
![Western Blot: TRPM7 Antibody [NBP3-23362] - Western blot image of human autophosphorylated TRPM7 C-terminal kinase domain (lanes 1-6). The blot was treated with lambda phosphatase to dephosphorylate TRPM7 phosphosites (lanes 2, 4, & 6). The blot was probed with rabbit polyclonals anti-TRPM7 (Ser-1513) phospho-specific (lanes 1 & 2), anti-TRPM7 (a.a.1484-1497) NBP3-23362 antibody (lanes 3 & 4), or anti-TRPM7 (Ser-1493) phospho-specific (lanes 5 & 6).](http://images.novusbio.com/fullsize/nbp3-23362_rabbit-trpm7-pab-19920231252368.jpg "<b>Biological Strategies Validation. </b>Western Blot: TRPM7 Antibody [NBP3-23362] - Western blot image of human autophosphorylated TRPM7 C-terminal kinase domain (lanes 1-6). The blot was treated with lambda phosphatase to dephosphorylate TRPM7 phosphosites (lanes 2, 4, & 6). The blot was probed with rabbit polyclonals anti-TRPM7 (Ser-1513) phospho-specific (lanes 1 & 2), anti-TRPM7 (a.a.1484-1497) NBP3-23362 antibody (lanes 3 & 4), or anti-TRPM7 (Ser-1493) phospho-specific (lanes 5 & 6).")
![Immunocytochemistry/ Immunofluorescence: NMDAR2B Antibody (17) - BSA Free [NBP3-43543] - Immunofluorescence analysis of paraformaldehyde fixed C6 cells stained with NBP3-43543 at 10 µg/ml for 1h followed by Alexa Fluor® 488 secondary antibody (2 µg/ml), showing membrane staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP3-43543, 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/nbp3-43543_mouse-nmdar2b-mab-17-azide-and-bsa-free-immunocytochemistry-immunofluorescence-2220260322015.png "Immunocytochemistry/ Immunofluorescence: NMDAR2B Antibody (17) - BSA Free [NBP3-43543] - Immunofluorescence analysis of paraformaldehyde fixed C6 cells stained with NBP3-43543 at 10 µg/ml for 1h followed by Alexa Fluor® 488 secondary antibody (2 µg/ml), showing membrane staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP3-43543, 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: NMDAR2B Antibody (17) - BSA Free [NBP3-43543] - Paraformaldehyde fixed C6 cells permeabilized with 0.5% Triton were stained with anti-unknown specificity antibody (isotype control, black line) or NBP3-43543 (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/nbp3-43543_mouse-nmdar2b-mab-17-azide-and-bsa-free-flow-cytometry-222026035556.png)
![Western Blot: TRPM7 [p Ser1493] Antibody [NBP3-23179] - Western blot image of human autophosphorylated TRPM7 C-terminal kinase domain (lanes 1-6). The blot was treated with lambda phosphatase to dephosphorylate TRPM7 phosphosites (lanes 2, 4, & 6). The blot was probed with rabbit polyclonals anti-TRPM7 (Ser-1513) phospho-specific (lanes 1 & 2), anti-TRPM7 (a.a.1484-1497) NBP3-23362 antibody (lanes 3 & 4), or anti-TRPM7 (Ser-1493) phospho-specific (lanes 5 & 6).](http://images.novusbio.com/fullsize/nbp3-23179_rabbit-trpm7-p-ser1493-pab-11920231633161.jpg "<b>Biological Strategies Validation. </b>Western Blot: TRPM7 [p Ser1493] Antibody [NBP3-23179] - Western blot image of human autophosphorylated TRPM7 C-terminal kinase domain (lanes 1-6). The blot was treated with lambda phosphatase to dephosphorylate TRPM7 phosphosites (lanes 2, 4, & 6). The blot was probed with rabbit polyclonals anti-TRPM7 (Ser-1513) phospho-specific (lanes 1 & 2), anti-TRPM7 (a.a.1484-1497) NBP3-23362 antibody (lanes 3 & 4), or anti-TRPM7 (Ser-1493) phospho-specific (lanes 5 & 6).")
![Immunohistochemistry: Niemann-Pick type C1 Like-1 Antibody (4B10) [NBP3-15211] - IHC image of Niemann-Pick type C1 Like-1 antibody diluted at 1:100 and staining in paraffin-embedded human liver tissue. 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 30 minutes 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/Niemann-Pick-type-C1-Like-1-Antibody-4B10-Immunohistochemistry-NBP3-15211-img0001.jpg "Immunohistochemistry: Niemann-Pick type C1 Like-1 Antibody (4B10) [NBP3-15211] - IHC image of Niemann-Pick type C1 Like-1 antibody diluted at 1:100 and staining in paraffin-embedded human liver tissue. 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 30 minutes 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: SMN Antibody (8B10) [NBP3-26312] - Image of SMN Antibody (8B10) diluted at 1:100 and staining in paraffin-embedded human kidney 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/nbp3-26312_rabbit-smn-mab-8b10-26220241522418.jpg "Immunohistochemistry: SMN Antibody (8B10) [NBP3-26312] - Image of SMN Antibody (8B10) diluted at 1:100 and staining in paraffin-embedded human kidney 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.")