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![ELISA: Human SUR1 - Ready-To-Use ELISA Kit (Colorimetric) [NBP3-31125] - Standard Curve Reference](http://images.novusbio.com/fullsize/nbp3-31125_human-sur1-ready-to-use-elisa-kit-colorimetric-20620241533972.png "ELISA: Human SUR1 - Ready-To-Use ELISA Kit (Colorimetric) [NBP3-31125] - Standard Curve Reference")
![ELISA: Human LAMP-2/CD107b ELISA Kit (Colorimetric) [NBP3-40063] - Standard Curve Reference](http://images.novusbio.com/fullsize/nbp3-40063_human-lamp-2-cd107b-elisa-kit-colorimetric-2110202415362343.png "ELISA: Human LAMP-2/CD107b ELISA Kit (Colorimetric) [NBP3-40063] - Standard Curve Reference")
![ELISA: Human LRP2 ELISA Kit (Colorimetric) [NBP3-40030] - Standard Curve Reference](http://images.novusbio.com/fullsize/nbp3-40030_human-lrp2-elisa-kit-colorimetric-2110202415393735.png "ELISA: Human LRP2 ELISA Kit (Colorimetric) [NBP3-40030] - Standard Curve Reference")
![ELISA: Human LRP2 - Ready-To-Use ELISA Kit (Colorimetric) [NBP3-40031] - Standard Curve Reference](http://images.novusbio.com/fullsize/nbp3-40031_human-lrp2-ready-to-use-elisa-kit-colorimetric-2110202415393786.png "ELISA: Human LRP2 - Ready-To-Use ELISA Kit (Colorimetric) [NBP3-40031] - Standard Curve Reference")
![Flow Cytometry: LRP2 Antibody (10B5) [NBP3-26163] - Overlay Peak curve showing MCF7 cells stained with LRP2 Antibody (10B5) (red line) at 1:100. 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/nbp3-26163_rabbit-lrp2-mab-10b5-282202414183627.jpg "Flow Cytometry: LRP2 Antibody (10B5) [NBP3-26163] - Overlay Peak curve showing MCF7 cells stained with LRP2 Antibody (10B5) (red line) at 1:100. 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.")