| Field | Specification |
|---|---|
| Mfr No | |
| Alternative Names | MMP-X1; MT1-MMP; MTMMP1; Membrane Inserted; Membrane-type matrix metalloproteinase 1; Membrane-type-1 matrix metalloproteinase |
| Assay Time | |
| Assay Type | |
| Detection Range | |
| Product Type | |
| Reactivity | |
| Sample Type(s) | serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids |
| Sensitivity | |
| Target | |
| UniProt # |
Scientific background
MMP14(Matrix Metalloproteinase 14) Microsample is a matrix metalloproteinase-related enzyme marker linked to extracellular matrix (ECM) remodeling.
MMP levels are frequently tracked in studies of inflammation, fibrosis, wound healing, and cancer invasion/metastasis where ECM turnover is important.
Because MMP regulation can involve secretion, activation, and inhibition, protein quantification supports a fuller interpretation alongside functional assays.
Why it matters
- Quantify MMP14(Matrix Metalloproteinase 14) Microsample to compare biological changes across conditions, doses, or time points.
- Generate concentration data from a standard curve to support biomarker and mechanistic studies.
How the ELISA works
Designed for Rat samples, this kit uses a The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Rat MMP14. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat MMP14. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Rat MMP14, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Rat MMP14 in the samples is then determined by comparing the OD of the samples to the standard curve.. After binding and washing, signal is converted to concentration using a standard curve.
Sample types: serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids.
- Detection range: 0.32-20 ng/mL
- Sensitivity/LoD: 0.12 ng/mL
- Assay time: 3.5h
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