| Field | Specification |
|---|---|
| Mfr No | |
| Alternative Names | TSG6; TNF-Stimulated Gene 6; Hyaluronate-binding protein; Tumor necrosis factor alpha-induced protein 6 |
| Assay Time | |
| Assay Type | |
| Detection Range | |
| Product Type | |
| Reactivity | |
| Sample Type(s) | serum, plasma, tissue homogenates and other biological fluids |
| Sensitivity | |
| Target |
Scientific background
TNFaIP6 (Tumor Necrosis Factor Alpha Induced Protein 6) is a TNF-family inflammatory mediator involved in cytokine cascades and cell fate signaling (survival/apoptosis), depending on context.
TNF-pathway markers are commonly monitored in innate immune activation and inflammatory disease models and can respond to endotoxin or immune-modulating treatments.
Protein-level quantification helps compare cohorts and treatment effects, especially when transcriptional changes do not directly predict secreted protein abundance.
Why it matters
- Quantify TNFaIP6 (Tumor Necrosis Factor Alpha Induced Protein 6) 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 TNFaIP6. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat TNFaIP6. 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 TNFaIP6, 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 TNFaIP6 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 and other biological fluids.
- Detection range: 0.16-10 ng/mL
- Sensitivity/LoD: 0.051 ng/mL
- Assay time: 3.5h
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