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![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.")
![ELISA: Monkey TNF-alpha ELISA Kit (Colorimetric) [NBP1-94190] - Representative standard curve for monkey TNF alpha total ELISA.Monkey TNF alpha was diluted in serial 2-fold steps in Sample Diluent.Do not use this standard curve to derive test results. A standard curvemust be run for each group of microwell strips assayed.](http://images.novusbio.com/fullsize/Primate-TNF-alpha-ELISA-Kit-Colorimetric-ELISA-NBP1-94190-img0001.jpg "ELISA: Monkey TNF-alpha ELISA Kit (Colorimetric) [NBP1-94190] - Representative standard curve for monkey TNF alpha total ELISA.Monkey TNF alpha was diluted in serial 2-fold steps in Sample Diluent.Do not use this standard curve to derive test results. A standard curvemust be run for each group of microwell strips assayed.")
![Flow Cytometry: CD59 Antibody (28D4) [NBP3-26676] - Overlay Peak curve showing Hela cells stained with CD59 Antibody (28D4) (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/nbp3-26676_rabbit-cd59-mab-28d4-282202414183671.jpg "Flow Cytometry: CD59 Antibody (28D4) [NBP3-26676] - Overlay Peak curve showing Hela cells stained with CD59 Antibody (28D4) (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: DARC Antibody (18B11) [NBP3-26634] - Overlay Peak curve showing 293 cells stained with DARC Antibody (18B11) (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/nbp3-26634_rabbit-darc-mab-18b11-282202414183683.jpg "Flow Cytometry: DARC Antibody (18B11) [NBP3-26634] - Overlay Peak curve showing 293 cells stained with DARC Antibody (18B11) (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.")