Fluorescence in situ Hybridization (FISH)
This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.
Specimen requirements | |
|---|---|
| Patient preparation | None Specified |
| Preferred specimen(s) | 3 mL bone marrow or 5 mL whole blood collected in a sodium heparin (green-top) tube |
| Alternative specimen(s) | Bone marrow collected in: Transport medium, sodium heparin (royal blue-top) tube or sodium heparin lead free (tan-top) tube • Whole blood collected in: Sodium heparin (royal blue-top) tube or sodium heparin lead free (tan-top) tube • 5x5 mm fresh tumor tissue in transport medium • 5x5 mm tumor tissue in formalin-fixed, paraffin-embedded tissue block |
| Minimum volume | 1 mL bone marrow • 3 mL whole blood |
| Transport container | Sodium heparin (green-top) tube |
| Transport temperature | Room temperature |
| Specimen stability | Specimen viability decreases during transit. Send specimen to testing lab for viability determination. Do not freeze. Do not reject. |
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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