| Sub Cat | Reactivity | Sensitivity | Detection Range | |
| MTS-1123-HM322 | Pig | 100-2500 pg/mL | Inquiry | |
| MTS-1123-HM323 | Cow | User optimized | Inquiry | |
| MTS-1123-HM324 | Goat | User optimized | Inquiry | |
| MTS-1123-HM325 | Human | 25-500 pg/mL | Inquiry | |
| MTS-1123-HM326 | Chicken | User optimized | Inquiry | |
| MTS-1123-HM327 | Monkey | User optimized | Inquiry | |
| MTS-1123-HM328 | Sheep | 250-5000 pg/mL | Inquiry | |
| MTS-1123-HM329 | Rat | 250-5000 pg/mL | Inquiry |
The indexed description states this is a competition ELISA kit with colorimetric detection for quantitative measurement of CXCL2. Competitive designs can be useful when you prefer that assay principle or want an alternative to sandwich ELISA in your workflow. Keep in mind that competitive assays often have inverse signal behavior, so standards and controls are especially important for correct interpretation.
In large runs, errors most often come from curve direction confusion, inconsistent timing, or choosing dilutions that land on insensitive curve regions. We recommend a pilot plate first: confirm the inverse relationship on your standard curve, then select a dilution that places most samples in the steep part of the curve. Include duplicates and a reference control on every plate. These steps dramatically reduce the chance of wrong conclusions in big datasets.
Yes, it's described for quantitative measurement, but publication-quality reporting depends on execution: duplicates, complete standard curves, and documented quality checks (CV thresholds, control acceptance ranges). If you're comparing multiple matrices (e.g., plasma vs supernatant), validate dilution linearity and recovery for each matrix separately. For high-stakes endpoints, consider confirming a subset with an orthogonal approach to strengthen confidence and reviewer acceptance.
For Research Use Only. Do Not Use in Food Manufacturing or Medical Procedures (Diagnostics or Therapeutics). Do Not Use in Humans.