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![ELISA: Complement Component C5aR1 Antibody (3A7) [NBP3-26470] - The Binding Activity of Human Complement Component C5aR1 with Complement Component C5aR1 Antibody. Activity: Measured by its binding ability in a functional ELISA. Immobilized Human Complement Component C5aR1 at 10 ug/mL can bind Complement Component C5aR1 Antibody, the EC50 is 1.239-3.760 ng/mL.](http://images.novusbio.com/fullsize/nbp3-26470_human-complement-component-c5ar1-mab-3a7-262202412272333.jpg "ELISA: Complement Component C5aR1 Antibody (3A7) [NBP3-26470] - The Binding Activity of Human Complement Component C5aR1 with Complement Component C5aR1 Antibody. Activity: Measured by its binding ability in a functional ELISA. Immobilized Human Complement Component C5aR1 at 10 ug/mL can bind Complement Component C5aR1 Antibody, the EC50 is 1.239-3.760 ng/mL.")
![Mouse CCL2/MCP1 ELISA Kit [NBP1-92659] - Data for Mouse MCP-1 Platinum ELISA](http://images.novusbio.com/fullsize/Mouse-CCL2-MCP1-ELISA-Kit-NBP1-92659-img0001.jpg "Mouse CCL2/MCP1 ELISA Kit [NBP1-92659] - Data for Mouse MCP-1 Platinum ELISA")
![Flow Cytometry: Histamine H3R Antibody (27H8) [NBP3-26219] - Overlay Peak curve showing SH-SY5Y cells stained with Histamine H3R Antibody (27H8) (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/nbp3-26219_rabbit-histamine-h3r-mab-27h8-282202414183626.jpg "Flow Cytometry: Histamine H3R Antibody (27H8) [NBP3-26219] - Overlay Peak curve showing SH-SY5Y cells stained with Histamine H3R Antibody (27H8) (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: Porcine IL-18/IL-1F4 ELISA Kit (Colorimetric) [NBP1-94192]](http://images.novusbio.com/fullsize/Porcine-IL-18-IL-1F4-ELISA-Kit-Colorimetric-ELISA-NBP1-94192-img0001.jpg "ELISA: Porcine IL-18/IL-1F4 ELISA Kit (Colorimetric) [NBP1-94192]")
![Flow Cytometry: CCR8 Antibody (2C6) [NBP3-26686] - Untransfected HEK293T cells (green line) and transfected Human CCR8 HEK293T stable cells (red line) were stained with anti-CCR8 antibody (2ug/1*10^6 cells), washed and then followed by FITC-conjugated anti-Human IgG Fc antibody and analyzed with flow cytometry.](http://images.novusbio.com/fullsize/nbp3-26686_human-ccr8-mab-2c6-28220241431276.jpg "Flow Cytometry: CCR8 Antibody (2C6) [NBP3-26686] - Untransfected HEK293T cells (green line) and transfected Human CCR8 HEK293T stable cells (red line) were stained with anti-CCR8 antibody (2ug/1*10^6 cells), washed and then followed by FITC-conjugated anti-Human IgG Fc antibody and analyzed with flow cytometry.")