| Field | Specification |
|---|---|
| Mfr No | |
| Alternative Names | JTK1; Non-Receptor Tyrosine-Protein Kinase TYK2 |
| Assay Time | |
| Assay Type | |
| Detection Range | |
| Product Type | |
| Reactivity | |
| Sample Type(s) | tissue homogenates, cell lysates and other biological fluids |
| Sensitivity | |
| Target | |
| UniProt # |
Scientific background
Tyk2 (Tyrosine Kinase 2) is associated with intracellular signaling regulation, often within phosphorylation-dependent pathways that control activation, proliferation, or differentiation.
While kinase activity is frequently assessed by phospho-readouts, total protein abundance can also shift with pathway rewiring, feedback, or changes in cell composition.
Protein quantification can complement phospho-specific assays and help interpret whether signaling changes are driven by abundance, activation state, or both.
Why it matters
- Quantify Tyk2 (Tyrosine Kinase 2) 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 Tyk2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human Tyk2. 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 Tyk2, 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 Tyk2 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: tissue homogenates, cell lysates and other biological fluids.
- Detection range: 0.32-20 ng/mL
- Sensitivity/LoD: 0.114 ng/mL
- Assay time: 3.5h
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