Note: Mouseover a species abbreviation on the product page to display the fullname.
How can we help you?
![ELISA: Primate IL-6 ELISA Kit [NBP1-92707]](http://images.novusbio.com/fullsize/Primate-IL-6-ELISA-Kit-ELISA-NBP1-92707-img0001.jpg "ELISA: Primate IL-6 ELISA Kit [NBP1-92707]")
![ELISA: Oncostatin M/OSM Antibody (31E7) [NBP3-26445] - The Binding Activity of Human Oncostatin M/OSM with Oncostatin M/OSM Antibody. Activity: Measured by its binding ability in a functional ELISA. Immobilized Human Oncostatin M/OSM at 2 ug/mL can bind Oncostatin M/OSM Antibody, the EC50 is 3.048-3.860 ng/mL.](http://images.novusbio.com/fullsize/nbp3-26445_human-oncostatin-m-osm-mab-31e7-262202412272325.jpg "ELISA: Oncostatin M/OSM Antibody (31E7) [NBP3-26445] - The Binding Activity of Human Oncostatin M/OSM with Oncostatin M/OSM Antibody. Activity: Measured by its binding ability in a functional ELISA. Immobilized Human Oncostatin M/OSM at 2 ug/mL can bind Oncostatin M/OSM Antibody, the EC50 is 3.048-3.860 ng/mL.")
![Human CD30/TNFRSF8 ELISA Kit [NBP1-91185] - Data for Human sCD30 Platinum ELISA](http://images.novusbio.com/fullsize/Human-CD30-TNFRSF8-ELISA-Kit-NBP1-91185-img0001.jpg "Human CD30/TNFRSF8 ELISA Kit [NBP1-91185] - Data for Human sCD30 Platinum ELISA")
![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.")