Myelin Antibody (IgG), IFA
Test code
CPT code(s)*
Test resources
Details
Methodology
Indirect Immunofluorescence
Assay category
This test was performed using a kit that has not been cleared or approved by the FDA. The analytical performance characteristics of this test have been determined by Quest Diagnostics. This test should not be used for diagnosis without confirmation by other medically established means.
Specimen requirements | |
|---|---|
| Patient preparation | None Specified |
| Preferred specimen(s) | 1 mL serum collected in a red-top tube (no gel) |
| Minimum volume | 0.3 mL |
| Collection instructions | Serum specimens should be collected under aseptic condition. Hemolysis should be avoided through prompt separation of the serum from the clot. |
| Transport container | Transport tube |
| Transport temperature | Room temperature |
| Specimen stability | Room temperature: 7 days Refrigerated: 14 days Frozen: 21 days |
| Reject criteria | Gross hemolysis • Lipemia • Specimens with visible particulate matter • Serum separator tube (SST) |
Reference ranges are provided as general guidance only. To interpret test results use the reference range in the laboratory report.
*The CPT codes provided are based on AMA guidance and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.
This material contains content from LOINC® (http://loinc.org). The LOINC Table, LOINC Table Core are copyright © 1995-2019, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee and is available at no cost under the license at http://loinc.org/license.
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