Interleukin 12, Plasma
Also known as: IL12 PLA
Use
The Interleukin 12, Plasma test is primarily used for research and supports attempts to understand the pathogenesis of immune, infectious, allergic, or inflammatory disorders. The results are used to understand the pathophysiology of these disorders and may contribute to ongoing research efforts.
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. Separate specimens must be submitted when multiple tests are ordered.
Limitations
This test was developed and its performance characteristics were determined by ARUP Laboratories. It has not been cleared or approved by the US Food and Drug Administration. However, it is performed in a CLIA certified laboratory and is intended for clinical purposes. Refrigerated specimens and contaminated or heat-inactivated specimens are unacceptable.
New York Approved
Methodology
Immunoassay (Multiplex Protein Panel)
Biomarkers
LOINC Codes
- 41760-0
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
Separate plasma from cells ASAP or within 2 hours of collection.
Storage Instructions
CRITICAL FROZEN.
Causes for Rejection
Refrigerated specimens. Contaminated or heat-inactivated specimens.
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 30 minutes |
| Refrigerated | Unacceptable |
| Frozen | 1 year |