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![ELISA: Caspase-9 ELISA Kit [NBP1-83734] - Standard curve](http://images.novusbio.com/fullsize/Caspase-9-ELISA-Kit-ELISA-NBP1-83734-img0001.jpg "ELISA: Caspase-9 ELISA Kit [NBP1-83734] - Standard curve")
![Flow Cytometry: Serum Amyloid A1 Antibody (20G5) [NBP3-26337] - Overlay Peak curve showing HepG2 cells stained with Serum Amyloid A1 Antibody (20G5) (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/nbp3-26337_rabbit-serum-amyloid-a1-mab-20g5-282202414312752.jpg "Flow Cytometry: Serum Amyloid A1 Antibody (20G5) [NBP3-26337] - Overlay Peak curve showing HepG2 cells stained with Serum Amyloid A1 Antibody (20G5) (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.")
![Bovine alpha 2-Macroglobulin ELISA Kit (Colorimetric) [NBP2-77018] - Standard Curve Reference](http://images.novusbio.com/fullsize/nbp2-77018_bovine-alpha-2-macroglobulin-elisa-kit-colorimetric-3120248504644.png "Bovine alpha 2-Macroglobulin ELISA Kit (Colorimetric) [NBP2-77018] - Standard Curve Reference")
![Flow Cytometry: Mitofusin 1 Antibody (11G8) [NBP3-26143] - Overlay Peak curve showing HepG2 cells stained with Mitofusin 1 Antibody (11G8) (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/nbp3-26143_rabbit-mitofusin-1-mab-11g8-282202414312714.jpg "Flow Cytometry: Mitofusin 1 Antibody (11G8) [NBP3-26143] - Overlay Peak curve showing HepG2 cells stained with Mitofusin 1 Antibody (11G8) (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.")