| Sub Cat | Reactivity | Sensitivity | Detection Range | |
| MTS-1123-HM398 | Pig | User optimized | Inquiry | |
| MTS-1123-HM399 | Cow | User optimized | Inquiry | |
| MTS-1123-HM400 | Goat | User optimized | Inquiry | |
| MTS-1123-HM401 | Chicken | User optimized | Inquiry | |
| MTS-1123-HM402 | Sheep | User optimized | Inquiry | |
| MTS-1123-HM403 | Human | 5.0-100 U/L | Inquiry |
Competitive assays can be attractive when you expect a broad range of cytokine levels, when sample matrix is complex, or when competitive format better matches available antibody performance. If your samples swing from very low to very high CSF2, competition can help avoid saturation once the dilution factor is optimized. We recommend a quick pilot dilution series to establish a stable operating point before scaling.
The hands-on workflow is similar to other ELISAs, but interpretation differs because signal often decreases as analyte increases. Data analysis typically uses a standard curve and curve fitting like other immunoassays; the key is consistent plate setup and correct curve direction. We can provide guidance on plotting, control placement, and QC checks so results remain easy to review and defensible.
Competitive formats can be sensitive to small pipetting errors, especially in standards. We recommend careful serial dilutions with thorough mixing, using calibrated pipettes, and running standards in duplicates or triplicates. Standardizing incubation times and wash steps also matters. If you run many plates, include the same QC sample on every plate to detect drift early and correct workflow issues before they compound.
For Research Use Only. Do Not Use in Food Manufacturing or Medical Procedures (Diagnostics or Therapeutics). Do Not Use in Humans.