Interleukin 17, Serum
Also known as: IL17
Use
This test is primarily used for research and to support understanding the pathogenesis of immune, infectious, allergic, or inflammatory disorders. The results help understand the pathophysiology of these conditions, which may guide therapeutic decisions or contribute to ongoing research efforts.
Special Instructions
Cytokine levels may demonstrate diurnal variation. It is recommended to determine cytokine levels at the same time of day for longitudinal comparison. Separate specimens must be submitted when multiple tests are ordered.
Limitations
The test has not been cleared or approved by the FDA. It is intended for clinical purposes and was developed and its performance characteristics determined by ARUP Laboratories. The results are used to understand immune, infectious, or inflammatory disorders or for research purposes.
New York Approved
Methodology
Immunoassay (Multiplex Protein Panel)
Biomarkers
LOINC Codes
- 82334-4
Result Turnaround Time
1-4 days
Related Documents
For more information, please review the documents below
Specimen
Serum
Volume
1 mL
Minimum Volume
0.4 mL
Container
ARUP Standard Transport Tube.
Collection Instructions
Separate from cells ASAP or within 2 hours of collection. Transfer serum to an ARUP Standard Transport Tube.
Storage Instructions
CRITICAL FROZEN
Causes for Rejection
Contaminated or heat-inactivated specimens.
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 30 minutes |
| Refrigerated | Unacceptable |
| Frozen | 1 year |