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![ELISA: Human NELL2 ELISA Kit (Colorimetric) [NBP3-39107] - Standard Curve Reference](http://images.novusbio.com/fullsize/nbp3-39107_human-nell2-elisa-kit-colorimetric-2110202415334946.png "ELISA: Human NELL2 ELISA Kit (Colorimetric) [NBP3-39107] - Standard Curve Reference")
![ELISA: Human MeCP2 ELISA Kit (Colorimetric) [NBP3-39862] - Standard Curve Reference](http://images.novusbio.com/fullsize/nbp3-39862_human-mecp2-elisa-kit-colorimetric-2110202415384020.png "ELISA: Human MeCP2 ELISA Kit (Colorimetric) [NBP3-39862] - Standard Curve Reference")
![ELISA: Human Orexin - Ready-To-Use ELISA Kit (Colorimetric) [NBP3-39223] - Standard Curve Reference](http://images.novusbio.com/fullsize/nbp3-39223_human-orexin-ready-to-use-elisa-kit-colorimetric-2110202415273841.png "ELISA: Human Orexin - Ready-To-Use ELISA Kit (Colorimetric) [NBP3-39223] - Standard Curve Reference")
![Immunocytochemistry/ Immunofluorescence: Nicotinic Acetylcholine Receptor beta 2 Antibody (12H2) - BSA Free [NBP3-43572] - Immunofluorescence analysis of paraformaldehyde fixed Kelly cells on coverslips stained with the chimeric version of this antibody, NBP3-43573 (1:100 dilution) for 1h followed by Alexa Fluor® 488 secondary antibody (1:1000 dilution), showing membrane staining. The nuclear stain is DAPI (blue). Panels show, from left-right, top-bottom, NBP3-43573, 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/nbp3-43572_mu-nicotinic-acetylcholine-r-beta-2-mab-12h2-azide-bsa-free-immunocytochemistry-immunofluorescence-222026035111.png "Immunocytochemistry/ Immunofluorescence: Nicotinic Acetylcholine Receptor beta 2 Antibody (12H2) - BSA Free [NBP3-43572] - Immunofluorescence analysis of paraformaldehyde fixed Kelly cells on coverslips stained with the chimeric version of this antibody, NBP3-43573 (1:100 dilution) for 1h followed by Alexa Fluor® 488 secondary antibody (1:1000 dilution), showing membrane staining. The nuclear stain is DAPI (blue). Panels show, from left-right, top-bottom, NBP3-43573, 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: Nicotinic Acetylcholine Receptor beta 2 Antibody (12H2) - Chimeric - BSA Free [NBP3-43573] - Immunofluorescence analysis of paraformaldehyde fixed Kelly cells on coverslips stained with NBP3-43573 (1:100 dilution) for 1h followed by Alexa Fluor® 488 secondary antibody (1:1000 dilution), showing membrane staining. The nuclear stain is DAPI (blue). Panels show, from left-right, top-bottom, NBP3-43573, 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/nbp3-43573_rb-nicotinic-ach-r-beta-2-mab-12h2-chimeric-azide-bsa-free-immunocytochemistry-immunofluorescence-2220260351110.png "Immunocytochemistry/ Immunofluorescence: Nicotinic Acetylcholine Receptor beta 2 Antibody (12H2) - Chimeric - BSA Free [NBP3-43573] - Immunofluorescence analysis of paraformaldehyde fixed Kelly cells on coverslips stained with NBP3-43573 (1:100 dilution) for 1h followed by Alexa Fluor® 488 secondary antibody (1:1000 dilution), showing membrane staining. The nuclear stain is DAPI (blue). Panels show, from left-right, top-bottom, NBP3-43573, DAPI, merged channels, and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor® 488 secondary antibody.")
![ELISA: Cannabinoid R1/CB1/CNR1 Antibody (2A1) [NBP3-26648] - The Binding Activity of Human Cannabinoid R1/CB1/CNR1 with Cannabinoid R1/CB1/CNR1 Antibody. Activity: Measured by its binding ability in a functional ELISA. Immobilized Human Cannabinoid R1/CB1/CNR1 at 10 ug/mL can bind Cannabinoid R1/CB1/CNR1 Antibody, the EC50 is 41.72-63.54 ng/mL.](http://images.novusbio.com/fullsize/nbp3-26648_human-cannabinoid-r1-cb1-cnr1-mab-2a1-262202412272348.jpg "ELISA: Cannabinoid R1/CB1/CNR1 Antibody (2A1) [NBP3-26648] - The Binding Activity of Human Cannabinoid R1/CB1/CNR1 with Cannabinoid R1/CB1/CNR1 Antibody. Activity: Measured by its binding ability in a functional ELISA. Immobilized Human Cannabinoid R1/CB1/CNR1 at 10 ug/mL can bind Cannabinoid R1/CB1/CNR1 Antibody, the EC50 is 41.72-63.54 ng/mL.")
![Flow Cytometry: NMDAR1 Antibody (24F5) [NBP3-26543] - Overlay Peak curve showing SH-SY5Y cells stained with NMDAR1 Antibody (24F5) (red line) at 1:50. The cells were fixed in 4% formaldehyde and permeated by 0.2% Triton X-100. Then 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10^6 cells) for 45min at 4C. The secondary antibody used was FITC-conjugated Goat Anti-rabbit IgG (H+L) at 1:200 dilution for 35min at 4C. Control antibody (green line) was rabbit IgG (1ug/1*10^6 cells) used under the same conditions. Acquisition of >10,000 events was performed.](http://images.novusbio.com/fullsize/nbp3-26543_rabbit-nmdar1-mab-24f5-282202414312771.jpg "Flow Cytometry: NMDAR1 Antibody (24F5) [NBP3-26543] - Overlay Peak curve showing SH-SY5Y cells stained with NMDAR1 Antibody (24F5) (red line) at 1:50. The cells were fixed in 4% formaldehyde and permeated by 0.2% Triton X-100. Then 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10^6 cells) for 45min at 4C. The secondary antibody used was FITC-conjugated Goat Anti-rabbit IgG (H+L) at 1:200 dilution for 35min at 4C. Control antibody (green line) was rabbit IgG (1ug/1*10^6 cells) used under the same conditions. Acquisition of >10,000 events was performed.")