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![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")
![ELISA: IL-21 ELISA Kit [NBP1-84816] - Standard curve](http://images.novusbio.com/fullsize/IL-21-ELISA-Kit-ELISA-NBP1-84816-img0001.jpg "ELISA: IL-21 ELISA Kit [NBP1-84816] - Standard curve")
![Flow Cytometry: CD3 zeta Antibody (21H6) [NBP3-26684] - Overlay Peak curve showing Jurkat cells stained with CD3 zeta Antibody (21H6) (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/nbp3-26684_rabbit-cd3-zeta-mab-21h6-282202414312735.jpg "Flow Cytometry: CD3 zeta Antibody (21H6) [NBP3-26684] - Overlay Peak curve showing Jurkat cells stained with CD3 zeta Antibody (21H6) (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: IL12B Antibody (10B10) [NBP3-26203] - Overlay Peak curve showing A549 cells stained with IL12B Antibody (10B10) (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/nbp3-26203_rabbit-il12b-mab-10b10-28220241431278.jpg "Flow Cytometry: IL12B Antibody (10B10) [NBP3-26203] - Overlay Peak curve showing A549 cells stained with IL12B Antibody (10B10) (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: CD133 Antibody (5F5) [NBP3-26366] - The Binding Activity of CD133 with CD133 Antibody. Activity: Measured by its binding ability in a functional ELISA. Immobilized CD133 at 5 ug/mL can bind CD133 Antibody, the EC50 is 0.4322-0.7189 ng/mL.](http://images.novusbio.com/fullsize/nbp3-26366_human-cd133-mab-5f5-26220241236350.jpg "ELISA: CD133 Antibody (5F5) [NBP3-26366] - The Binding Activity of CD133 with CD133 Antibody. Activity: Measured by its binding ability in a functional ELISA. Immobilized CD133 at 5 ug/mL can bind CD133 Antibody, the EC50 is 0.4322-0.7189 ng/mL.")
![ELISA: IL-12 ELISA Kit [Biotin] [NBP1-92677] - Standard curve](http://images.novusbio.com/fullsize/IL-12-ELISA-Kit-[Biotin]-ELISA-NBP1-92677-img0001.jpg "ELISA: IL-12 ELISA Kit [Biotin] [NBP1-92677] - Standard curve")