Initial test for prognostication of CN-AML.
Polymerase Chain Reaction/Sequencing
DNA isolation: Sun-Sat
Assay: Mon, Wed, Fri
New York DOH Approval Status
Lavender (EDTA) or bone marrow (EDTA).
Whole Blood: Do not freeze. Transport 5 mL whole blood (Min: 1 mL)
Bone Marrow: Transport 3 mL bone marrow. (Min: 1 mL)
Plasma, serum, FFPE tissue blocks/slides, or frozen tissue, DNA extracted by a non-CLIA lab. Specimens collected in anticoagulants other than EDTA or sodium heparin. Clotted or grossly hemolyzed specimens.
Ambient: 24 hours; Refrigerated: 5 days; Frozen: Unacceptable
Refer to report.
This test was developed and its performance characteristics determined by ARUP Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.
Laboratory Developed Test (LDT)
|Component Test Code*||Component Chart Name||LOINC|
|2004249||CEBPA Mutation Detection Results||64012-8|
- CCAAT Enhancer Binding Protein Alpha
- CEBP Alpha
- CEBPA Mutation Analysis