| Field | Specification |
|---|---|
| Mfr No | |
| Alternative Names | Malondialdehyde; MDA |
| Assay Time | |
| Assay Type | |
| Detection Range | |
| Product Type | |
| Reactivity | |
| Sample Type(s) | serum, plasma and other biological fluids |
| Sensitivity | |
| Target |
Scientific background
MDA (Malondialdehyde) is a biologically relevant protein marker measured to support mechanistic studies and biomarker discovery (context dependent).
Protein concentrations can change due to secretion, degradation, cell composition shifts, or post-transcriptional regulation, so ELISA readouts often add information beyond gene expression alone.
Quantitative measurements help compare groups and time points using standardized curves and can be interpreted alongside phenotype and pathway-specific readouts.
Why it matters
- Quantify MDA (Malondialdehyde) 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 This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Rat MDA. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat MDA. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. 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 MDA 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 and other biological fluids.
- Detection range: 31.25-2000 ng/mL
- Sensitivity/LoD: 9.13 ng/mL
- Assay time: 2h
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