| Sub Cat | Reactivity | Sensitivity | Detection Range | |
| MTS-1123-HM543 | Cow | 5-1000 pg/mL | Inquiry | |
| MTS-1123-HM544 | Chicken | 1-200 pg/mL | Inquiry | |
| MTS-1123-HM545 | Sheep | 5-80 pg/mL | Inquiry | |
| MTS-1123-HM546 | Rabbit | 50-1000 pg/mL | Inquiry | |
| MTS-1123-HM547 | Goat | 50-1000 pg/mL | Inquiry | |
| MTS-1123-HM548 | Chicken | 50-1000 pg/mL | Inquiry | |
| MTS-1123-HM549 | Mouse | 50-1000 pg/mL | Inquiry | |
| MTS-1123-HM550 | Rat | 50-1000 pg/mL | Inquiry | |
| MTS-1123-HM551 | Guinea Pig | 50-1000 pg/mL | Inquiry |
A competition ELISA can be preferred when target size/epitope availability or sample conditions make two-antibody "sandwiching" less ideal, or when you want a robust approach that tolerates certain matrix effects. This kit is described as a colorimetric, quantitative competition ELISA for IL‑10. If you anticipate epitope masking or need a format compatible with specific assay constraints, competition can be a strong option.
Yes. Even in a competition format, quantitative interpretation relies on a well-prepared standard curve and consistent incubation/handling. The kit is designed for quantitative measurement with a colorimetric readout. In practice, you'll run standards and unknowns together, ensure proper mixing and timing, and use replicate wells to reduce variance-especially important in competition assays where signal decreases with higher analyte.
Absolutely. With competition ELISA, common causes of flattened curves include incorrect standard dilution series, insufficient mixing, incubation temperature deviations, or plate washing issues. Because the method is colorimetric and quantitative, small procedural inconsistencies can noticeably impact curve shape. We recommend verifying pipette calibration, preparing fresh standards, increasing wash stringency, and confirming that sample concentrations fall within the expected working range.
For Research Use Only. Do Not Use in Food Manufacturing or Medical Procedures (Diagnostics or Therapeutics). Do Not Use in Humans.