| Sub Cat | Reactivity | Sensitivity | Detection Range | |
| MTS-1123-HM174 | Guinea Pig | 50-1000 pg/mL | Inquiry | |
| MTS-1123-HM175 | Rabbit | 50-1000 pg/mL | Inquiry | |
| MTS-1123-HM176 | Dog | 50-1000 pg/mL | Inquiry | |
| MTS-1123-HM177 | Goat | User optimized | Inquiry | |
| MTS-1123-HM178 | Cow | User optimized | Inquiry | |
| MTS-1123-HM179 | Chicken | User optimized | Inquiry | |
| MTS-1123-HM180 | Sheep | User optimized | Inquiry | |
| MTS-1123-HM181 | Mouse | 50-1000 pg/mL | Inquiry |
A competitive ELISA is a different binding format that can be advantageous in certain real-world sample conditions. Customers often choose it when they want a shorter run time (this kit is listed at about 1.5 hours) and when a competitive format better suits the analyte/antibody configuration they need. It isn't inherently "more accurate" in every case; rather, it's about selecting the format that behaves best with your matrix and expected concentration range. Competitive assays also require careful attention to the fact that signal can be inversely related to concentration, so plate setup and curve interpretation are especially important.
Great point-competitive ELISAs can trip people up because higher analyte can lead to lower signal. We recommend: (1) run the full standard curve in duplicate every plate until your team is fully confident; (2) include a mid-range "plate control" sample that you run on every plate to verify curve orientation and consistency; and (3) keep plate layout fixed so standards and controls always occupy the same wells/rows. If the control sample suddenly shifts, that's your early warning sign to check pipetting accuracy, incubation timing, and wash steps before trusting sample calls.
Tissue homogenates are listed as compatible sample types for this kit, but the key is clarity and consistency. After homogenization, centrifuge thoroughly to remove particulate matter, and consider a second clarification step if the supernatant is still cloudy. For fatty tissues, excess lipids can increase background or cause inconsistent binding; dilution and careful buffer selection usually help. We also advise running spike-and-recovery checks during your first pilot to confirm that the matrix is not suppressing signal. Once the pilot confirms acceptable recovery and dilution linearity, you can scale confidently.
For Research Use Only. Do Not Use in Food Manufacturing or Medical Procedures (Diagnostics or Therapeutics). Do Not Use in Humans.