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![Monkey Apolipoprotein E/ApoE ELISA Kit (Colorimetric) [NBP2-77037] - Standard Curve Reference](http://images.novusbio.com/fullsize/nbp2-77037_monkey-apolipoprotein-e-apoe-elisa-kit-colorimetric-3120248504640.png "Monkey Apolipoprotein E/ApoE ELISA Kit (Colorimetric) [NBP2-77037] - 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.")
![ELISA: Human L-Selectin/CD62L ELISA Kit (Colorimetric) [NBP1-84821] - Standard curve](http://images.novusbio.com/fullsize/Human-L-Selectin-CD62L-ELISA-Kit-Colorimetric-ELISA-NBP1-84821-img0001.jpg "ELISA: Human L-Selectin/CD62L ELISA Kit (Colorimetric) [NBP1-84821] - Standard curve")