| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-12017-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-09047-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-09048-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-09013-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-09012-0.025mg | |||
![ELISA: SARS-CoV-2 Spike Antibody (CR3022) - Azide and BSA Free [NBP2-90980] - ELISA plate coated with SARS-CoV-2 Spike Glycoprotein (S1), His-Tag (Insect Cells; grey line) and SARS-CoV-2 Spike Glycoprotein (S2), His-Tag (Insect Cells; yellow line) at concentrations of 5 ug/ml. A 3-fold serial dilution from 41.6 ng/ml was performed using NBP2-90980; from 370 ng/ml for NBP3-11813 and from 10000 ng/ml for NBP3-11776. Human IgM and human IgA were HRP-conjugated and for the detection of human IgG1 a 1:4000 dilution of HRP-labelled anti-human IgG antibody was used.](http://images.novusbio.com/fullsize/nbp3-11813_human-monoclonal-sars-cov-2-spike-antibody-cr3022-7420252228560.png "ELISA: SARS-CoV-2 Spike Antibody (CR3022) - Azide and BSA Free [NBP2-90980] - ELISA plate coated with SARS-CoV-2 Spike Glycoprotein (S1), His-Tag (Insect Cells; grey line) and SARS-CoV-2 Spike Glycoprotein (S2), His-Tag (Insect Cells; yellow line) at concentrations of 5 ug/ml. A 3-fold serial dilution from 41.6 ng/ml was performed using NBP2-90980; from 370 ng/ml for NBP3-11813 and from 10000 ng/ml for NBP3-11776. Human IgM and human IgA were HRP-conjugated and for the detection of human IgG1 a 1:4000 dilution of HRP-labelled anti-human IgG antibody was used.")
![Immunocytochemistry /Immunofluorescence: GABA-AR alpha 1 Antibody (1F4) - Chimeric - Azide and BSA Free [NBP3-09047] - Immunofluorescence analysis of paraformaldehyde fixed U251 cells on Shi-fix(TM) coverslips stained with NBP3-09047 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: NBP3-09047, 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/nbp3-09047_rabbit-monoclonal-gaba-ar-alpha-1-antibody-1f4-chimeric-74202522141247.png "Immunocytochemistry /Immunofluorescence: GABA-AR alpha 1 Antibody (1F4) - Chimeric - Azide and BSA Free [NBP3-09047] - Immunofluorescence analysis of paraformaldehyde fixed U251 cells on Shi-fix(TM) coverslips stained with NBP3-09047 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: NBP3-09047, 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: 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)
![ELISA: Birch pollen Bet V1 Antibody (M0418) - Chimeric [NBP3-09013] - ELISA Plate coated with Birch pollen Bet V1 at a concentration of 2 ug/ml. A 3-fold serial dilution from 10,000 to 0.1 ng/ml was performed using NBP3-09013. For detection, a 1:4000 dilution of HRP-labelled goat anti-rabbit antibody was used. Absorbance at 450nm does not reach a plateau but falls slightly before increasing once more. This is suggestive of two binding sites on Birch pollen Bet V1 for which NBP3-09013 has differing affinities.](http://images.novusbio.com/fullsize/Birch-pollen-Bet-V1-Antibody-M0418-Chimeric-ELISA-NBP3-09013-img0001.jpg "ELISA: Birch pollen Bet V1 Antibody (M0418) - Chimeric [NBP3-09013] - ELISA Plate coated with Birch pollen Bet V1 at a concentration of 2 ug/ml. A 3-fold serial dilution from 10,000 to 0.1 ng/ml was performed using NBP3-09013. For detection, a 1:4000 dilution of HRP-labelled goat anti-rabbit antibody was used. Absorbance at 450nm does not reach a plateau but falls slightly before increasing once more. This is suggestive of two binding sites on Birch pollen Bet V1 for which NBP3-09013 has differing affinities.")