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![ELISA: Human EEA1 ELISA Kit (Colorimetric) [NBP3-31491] - Standard Curve Reference](http://images.novusbio.com/fullsize/nbp3-31491_human-eea1-elisa-kit-colorimetric-206202415322717.png "ELISA: Human EEA1 ELISA Kit (Colorimetric) [NBP3-31491] - Standard Curve Reference")
![ELISA: Human MEK1 - Ready-To-Use ELISA Kit (Colorimetric) [NBP3-39487] - Standard Curve Reference](http://images.novusbio.com/fullsize/nbp3-39487_human-mek1-ready-to-use-elisa-kit-colorimetric-2110202415393763.png "ELISA: Human MEK1 - Ready-To-Use ELISA Kit (Colorimetric) [NBP3-39487] - Standard Curve Reference")
![Flow Cytometry: Nanog Antibody (2G6) [NBP3-26119] - Overlay Peak curve showing Hela cells stained with Nanog Antibody (2G6) (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/nbp3-26119_rabbit-nanog-mab-2g6-282202414312711.jpg "Flow Cytometry: Nanog Antibody (2G6) [NBP3-26119] - Overlay Peak curve showing Hela cells stained with Nanog Antibody (2G6) (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.")
![Flow Cytometry: PEDFR/PNPLA2/ATGL Antibody (1H6) [NBP3-26374] - Overlay Peak curve showing HepG2 cells stained with PEDFR/PNPLA2/ATGL Antibody (1H6) (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/nbp3-26374_rabbit-pedfr-pnpla2-atgl-mab-1h6-282202414312727.jpg "Flow Cytometry: PEDFR/PNPLA2/ATGL Antibody (1H6) [NBP3-26374] - Overlay Peak curve showing HepG2 cells stained with PEDFR/PNPLA2/ATGL Antibody (1H6) (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.")
![Flow Cytometry: Beclin 1 Antibody (22F4) [NBP3-26478] - Overlay Peak curve showing RAJI cells stained with Beclin 1 Antibody (22F4) (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/nbp3-26478_rabbit-beclin-1-mab-22f4-282202414183664.jpg "Flow Cytometry: Beclin 1 Antibody (22F4) [NBP3-26478] - Overlay Peak curve showing RAJI cells stained with Beclin 1 Antibody (22F4) (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.")