Test Catalog

Test Id : FCYTP

Cytokine Panel 13

Method Name
A short description of the method used to perform the test

Quantitative Multiplex Bead Assay

NY State Available
Indicates the status of NY State approval and if the test is orderable for NY State clients.

Yes

Reporting Name
Lists a shorter or abbreviated version of the Published Name for a test

Cytokine Panel 13

Aliases
Lists additional common names for a test, as an aid in searching

Cytokine 12

IFN

IFN G

IFN gamma

IL 0

IL 1 B

IL 1 beta

IL 1

IL 10

IL 12 Receptor

IL 13

IL 17

IL 2

IL 2R

IL 4

IL 5

IL 6

IL 8

IL

IL2 Receptor Soluble

TNF alpha

Specimen Type
Describes the specimen type validated for testing

Varies

Specimen Required
Defines the optimal specimen required to perform the test and the preferred volume to complete testing

Serum

Draw blood in a plain, red-top tube(s), serum gel tube is acceptable. Spin down within 2 hours and send 1 mL of serum frozen in a plastic vial.

 

Note: Critical frozen. Additional specimens must be submitted when multiple tests are ordered.

Specimen Minimum Volume
Defines the amount of sample necessary to provide a clinically relevant result as determined by the Testing Laboratory

0.4 mL

Reject Due To
Identifies specimen types and conditions that may cause the specimen to be rejected

Hemolysis: NA
Thawing: Warm Reject; Cold Reject
Lipemia: NA
Icterus: NA
Other: Heat-inactivated, refrigerated or contaminated specimens are unacceptable.

Specimen Stability Information
Provides a description of the temperatures required to transport a specimen to the performing laboratory, alternate acceptable temperatures are also included

Specimen Type Temperature Time Special Container
Varies Frozen (preferred) 365 days

Reference Values
Describes reference intervals and additional information for interpretation of test results. May include intervals based on age and sex when appropriate. Intervals are Mayo-derived, unless otherwise designated. If an interpretive report is provided, the reference value field will state this.

Tumor Necrosis Factor-alpha

7.2  pg/mL or less

Interleukin 2

2.1 pg/mL or less

Interleukin 2 Receptor Soluble

175.3 pg/mL to 858.2 pg/mL

Interleukin 12

1.9 pg/mL or less

Interferon gamma

4.2 pg/mL or less

Interleukin 4

2.2  pg/mL or less

Interleukin 5

2.1  pg/mL or less

Interleukin 10

2.8  pg/mL or less

Interleukin 13

2.3  pg/mL or less

Interleukin 17

1.4  pg/mL or less

Interleukin 1 beta

6.7  pg/mL or less

Interleukin 6

2.0  pg/mL or less

Interleukin 8

3.0  pg/mL or less

 

Interpretation
Provides information to assist in interpretation of the test results

Results are used to understand the pathophysiology of immune, infectious, or inflammatory disorders, or may be used for research purposes.

PDF Report
Indicates whether the report includes an additional document with charts, images or other enriched information

No

Day(s) Performed
Outlines the days the test is performed. This field reflects the day that the sample must be in the testing laboratory to begin the testing process and includes any specimen preparation and processing time before the test is performed. Some tests are listed as continuously performed, which means that assays are performed multiple times during the day.

Monday, Wednesday, Friday

Report Available
The interval of time (receipt of sample at Mayo Clinic Laboratories to results available) taking into account standard setup days and weekends. The first day is the time that it typically takes for a result to be available. The last day is the time it might take, accounting for any necessary repeated testing.

1 to 8 days

Performing Laboratory Location
Indicates the location of the laboratory that performs the test

ARUP Laboratories

Fees
Several factors determine the fee charged to perform a test. Contact your U.S. or International Regional Manager for information about establishing a fee schedule or to learn more about resources to optimize test selection.

  • Authorized users can sign in to Test Prices for detailed fee information.
  • Clients without access to Test Prices can contact Customer Service 24 hours a day, seven days a week.
  • Prospective clients should contact their Regional Manager. For assistance, contact Customer Service.

Test Classification
Provides information regarding the medical device classification for laboratory test kits and reagents. Tests may be classified as cleared or approved by the US Food and Drug Administration (FDA) and used per manufacturer instructions, or as products that do not undergo full FDA review and approval, and are then labeled as an Analyte Specific Reagent (ASR) product.

This test was developed and its performance characteristics determined by ARUP Laboratories.

CPT Code Information
Provides guidance in determining the appropriate Current Procedural Terminology (CPT) code(s) information for each test or profile. The listed CPT codes reflect Mayo Clinic Laboratories interpretation of CPT coding requirements. It is the responsibility of each laboratory to determine correct CPT codes to use for billing.

CPT codes are provided by the performing laboratory.

83520 x 12

83529

LOINC® Information
Provides guidance in determining the Logical Observation Identifiers Names and Codes (LOINC) values for the order and results codes of this test. LOINC values are provided by the performing laboratory.

Test Id Test Order Name Order LOINC Value
FCYTP Cytokine Panel 13 82335-1
Result Id Test Result Name Result LOINC Value
Applies only to results expressed in units of measure originally reported by the performing laboratory. These values do not apply to results that are converted to other units of measure.
Z4722 Tumor Necrosis Factor - alpha 3074-2
Z4723 Interleukin 2 33939-0
Z4724 Interleukin 2 Receptor, Soluble 76039-7
Z4725 Interleukin 12 41760-0
Z4726 Interferon gamma 27415-9
Z4727 Interleukin 4 27161-9
Z4728 Interleukin 5 33938-2
Z4729 Interleukin 10 26848-2
Z4730 Interleukin 13 33822-8
Z4731 Interleukin 17 82334-4
Z4732 Interleukin 1 beta 13629-1
Z4733 Interleukin 6 26881-3
Z4734 Interleukin 8 33211-4

Test Setup Resources

Setup Files
Test setup information contains test file definition details to support order and result interfacing between Mayo Clinic Laboratories and your Laboratory Information System.

Excel | Pdf

Sample Reports
Normal and Abnormal sample reports are provided as references for report appearance.

Normal Reports | Abnormal Reports

SI Sample Reports
International System (SI) of Unit reports are provided for a limited number of tests. These reports are intended for international account use and are only available through MayoLINK accounts that have been defined to receive them.

SI Normal Reports | SI Abnormal Reports