Interleukin 17, Plasma
Also known as: IL17 PLA
Use
This test is primarily used for research and to support attempts to understand the pathogenesis of immune, infectious, allergic, or inflammatory disorders. Results are used to understand the pathophysiology of such conditions.
Special Instructions
Cytokine levels may demonstrate diurnal variation. For longitudinal comparison, it is recommended that cytokine levels be determined at the same time of day. New York state approved.
Limitations
This test was developed and its performance characteristics determined by ARUP Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test is intended for clinical purposes and is performed in a CLIA certified laboratory.
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
Plasma
Volume
1 mL
Minimum Volume
0.4 mL
Container
ARUP Standard Transport Tube
Collection Instructions
Collect in Green (Lithium Heparin). Separate plasma from cells ASAP or within 2 hours of collection.
Storage Instructions
CRITICAL FROZEN. Ship sample in an ARUP Standard Transport Tube.
Causes for Rejection
Contaminated or heat-inactivated specimens.
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 30 minutes |
| Refrigerated | Unacceptable |
| Frozen | 1 year |
Other tests from different labs that may be relevant