| Sub Cat | Reactivity | Sensitivity | Detection Range | |
| MTS-1123-HM454 | Human | 15.6 pg/mL-1000 pg/mL | Inquiry | |
| MTS-1123-HM455 | Human | 3.9-250 pg/mL | Inquiry | |
| MTS-1123-HM456 | Rat | 15.6 pg/mL-1000 pg/mL | Inquiry | |
| MTS-1123-HM457 | Mouse | 15.6 pg/mL-1000 pg/mL | Inquiry | |
| MTS-1123-HM458 | Rat | 31.2-2000 pg/mL | Inquiry | |
| MTS-1123-HM459 | Mouse | 12.5-800 pg/mL | Inquiry | |
| MTS-1123-HM460 | Rabbit | 7.8 pg/mL-500 pg/mL | Inquiry | |
| MTS-1123-HM461 | Mouse | 6.25 pg/mL-400 pg/mL | Inquiry | |
| MTS-1123-HM462 | Pig | 1.56 pg/mL-100 pg/mL | Inquiry | |
| MTS-1123-HM463 | Human | 125 pg/mL-8000 pg/mL | Inquiry | |
| MTS-1123-HM464 | Dog | 7.8 pg/mL-500 pg/mL | Inquiry | |
| MTS-1123-HM465 | Rabbit | 3.12 pg/mL-200 pg/mL | Inquiry | |
| MTS-1123-HM466 | Chicken | 7.8 pg/mL-500 pg/mL | Inquiry | |
| MTS-1123-HM467 | Cow | 15.6 pg/mL-1000 pg/mL | Inquiry | |
| MTS-1123-HM468 | Horse | 15.6 pg/mL-1000 pg/mL | Inquiry | |
| MTS-1123-HM469 | Fish | 3.12 pg/mL-200 pg/mL | Inquiry | |
| MTS-1123-HM470 | Goat | 15.625 pg/mL-1000 pg/mL | Inquiry | |
| MTS-1123-HM471 | Dog | 7.8 pg/mL-500 pg/mL | Inquiry | |
| MTS-1123-HM472 | Monkey | 7.8 pg/mL-500 pg/mL | Inquiry | |
| MTS-1123-HM473 | Sheep | 15.6 pg/mL-1000 pg/mL | Inquiry | |
| MTS-1123-HM474 | Rabbit | 3.12 pg/mL-200 pg/mL | Inquiry | |
| MTS-1123-HM475 | Cow | 15.6 pg/mL-1000 pg/mL | Inquiry | |
| MTS-1123-HM476 | Guinea Pig | 7.8 pg/mL-500 pg/mL | Inquiry | |
| MTS-1123-HM477 | Golden Syrian Hamster | 12.5 pg/mL-800 pg/mL | Inquiry | |
| MTS-1123-HM478 | Cat | 16-4.000 pg/mL | Inquiry | |
| MTS-1123-HM479 | Hamster | 12.5-800 pg/mL | Inquiry | |
| MTS-1123-HM480 | Rhesus Monkey | 7.8 pg/mL-500 pg/mL | Inquiry |
Yes, IL-1β is a classic inflammasome-associated cytokine, and a colorimetric ELISA is commonly used to quantify secretion changes after priming and activation. For best results, ensure that your workflow distinguishes pro-IL-1β induction from mature IL-1β secretion, and collect supernatants at consistent time points. Including relevant controls (e.g., priming-only vs priming + activation) helps interpret biology correctly.
You can compare within each model confidently, and cross-model comparisons are feasible if you standardize key variables. Use the same culture conditions where possible, match cell counts, and normalize stimulation intensity. Since different models can secrete different baseline levels, we recommend expressing results as fold-change versus matched controls, plus running an internal reference sample across plates to anchor inter-run consistency.
Debris can increase background and variability in any ELISA. We recommend centrifuging samples to remove particulates and transferring only the clear supernatant. If you must use crude samples, dilute them and consider running duplicates at two dilutions to confirm linearity. Clean handling and consistent washing steps usually solve most "noisy" IL-1β results without needing special equipment.
For Research Use Only. Do Not Use in Food Manufacturing or Medical Procedures (Diagnostics or Therapeutics). Do Not Use in Humans.