| Field | Specification |
|---|---|
| Mfr No | |
| Alternative Names | IFN gamma; IFN-G; IFG; IFI; INFr; IFN; Immune Interferon |
| 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
IFNg(Interferon Gamma) Microsample is part of interferon pathway biology that contributes to antiviral defense and immune regulation.
Interferon signaling can induce broad transcriptional programs; measuring interferon-related proteins helps contextualize pathway strength and timing in vivo and in vitro.
Interferon markers are often interpreted together with viral load, ISG expression, or immune activation markers to build a coherent response profile.
Why it matters
- Quantify IFNg(Interferon Gamma) 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 Human 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 Human IFNg. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human IFNg. 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 Human IFNg, 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 Human IFNg 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: 15.63-1000 pg/mL
- Sensitivity/LoD: 6 pg/mL
- Assay time: 3.5h
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