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HelpTest Code LCYP Cytokine Panel, 13 Analytes, Quantitative, Serum
Shipping Instructions
Specimen must be shipped frozen. Testing will be canceled if received ambient or refrigerated.
Specimen Required
Collection Container/Tube: Serum gel or red top
Submission Container/Tube: Plastic vial
Specimen Volume: 1 mL Serum
Collection Instructions:
1. As soon as possible and within 2 hours of collection, centrifuge and aliquot 1 mL of serum into a plastic vial.
2. Send frozen.
Note: Critical frozen. Separate specimens must be submitted when multiple tests are ordered.
Useful For
Aiding in the assessment of the pathophysiology of immune, infectious, or inflammatory disorders when used in conjunction with standard clinical assessment
May be used for research purposes
Method Name
Immunoassay
Reporting Name
Cytokine Panel, Quantitative, SSpecimen Type
SerumSpecimen Minimum Volume
Serum: 0.5 mL
Specimen Stability Information
| Specimen Type | Temperature | Time |
|---|---|---|
| Serum | Frozen | 30 days |
Reject Due To
| Heat-inactivated specimens | Reject |
| Contaminated specimens | Reject |
Reference Values
Tumor Necrosis Factor-alpha: ≤15.4 pg/mL
Interleukin 2: ≤1.3 pg/mL
Interleukin 2 Receptor Soluble: 353.0-1745 pg/mL
Interleukin 12: ≤1.8 pg/mL
Interferon gamma: ≤3.7 pg/mL
Interleukin 4: ≤1.0 pg/mL
Interleukin 5: ≤2.5 pg/mL
Interleukin 10: ≤2.9 pg/mL
Interleukin 13: ≤21.0 pg/mL
Interleukin 17: ≤1.3 pg/mL
Interleukin 1 beta: ≤5.7 pg/mL
Interleukin 6: ≤5.3 pg/mL
Interleukin 8: ≤20.7 pg/mL
Day(s) Performed
Tuesday, Thursday, Friday
Report Available
5 to 8 daysPerforming Laboratory
Progentec Diagnostics, IncTest Classification
Progentec Diagnostics testing uses an immunoassay to measure the concentrations of plasma proteins. Progentec Diagnostics developed and characterized this test. It is intended for clinical use and the reported results should be interpreted in relation to each patient's clinical condition and medical history. This test is a laboratory developed test (LDT) and is not cleared by the US Food and Drug Administration (FDA). FDA clearance is not currently required for LDTs. Progentec Diagnostics Clinical Laboratory is certified under the Clinical Laboratory Improvement Amendment (CLIA) of 1988 and accredited by the College of American Pathologists to perform high complexity clinical testing.CPT Code Information
83520 x 12
83529
LOINC Code Information
| Test ID | Test Order Name | Order LOINC Value |
|---|---|---|
| LCYP | Cytokine Panel, Quantitative, S | Not Provided |
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| CYP01 | Tumor Necrosis Factor alpha (TNF-a) | Not Provided |
| CYP02 | Interleukin 2 (IL-2) | Not Provided |
| CYP03 | Soluble Interleukin-2 Recep(sIL-2R) | Not Provided |
| CYP04 | Interleukin 12 (IL-12) | Not Provided |
| CYP05 | Interferon gamma (IFN-g) | Not Provided |
| CYP06 | Interleukin 4 (IL-4) | Not Provided |
| CYP07 | Interleukin 5 (IL-5) | Not Provided |
| CYP08 | Interleukin 10 (IL-10) | Not Provided |
| CYP09 | Interleukin 13 (IL-13) | Not Provided |
| CYP10 | Interleukin 17 (IL-17) | Not Provided |
| CYP11 | Interleukin 1 beta (IL-1b) | Not Provided |
| CYP12 | Interleukin 6 (IL-6) | Not Provided |
| CYP13 | Interleukin 8 (IL-8) | Not Provided |