Acute Lymphoblastic Leukemia (ALL) Panel by FISH, Adult
Recommended FISH panel for adults with newly diagnosed ALL.
Fluorescence in situ Hybridization (FISH)
New York DOH Approval Status
Non-diluted bone marrow aspirate collected in a heparinized syringe. Also acceptable: Whole blood in Green (Sodium Heparin).
Bone Marrow: Transfer 3 mL bone marrow to a Green (Sodium Heparin). (Min: 1 mL)
Whole Blood: Transport 5 mL whole blood. (Min: 2 mL)
Paraffin-embedded specimens. Clotted specimens.
Ambient: 48 hours; Refrigerated: 48 hours; Frozen: Unacceptable
Probes included: BCR/ABL, MLL, E2A, IGH, MYC
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.
Analyte Specific Reagent (ASR)
A processing fee will be charged if this procedure is canceled at the client's request, after the test has been set up, or if the sample integrity is inadequate to allow culture growth. To order probes separately, refer to Chromosome FISH, Interphase (2002298).
Other specimen types may be acceptable, contact the Cytogenetics Laboratory for specific specimen collection and transportation instructions.
If cell pellets or dropped cytogenetics slides are not submitted, a processing fee will apply.
This test must be ordered using Oncology test request form #43099 or through ARUP interface.
88271 x5; 88275 x5
|Component Test Code*||Component Chart Name||LOINC|
|2002648||ALL Panel by FISH, Adult||57802-1|
|2002649||EER ALL Panel by FISH, Adult||11526-1|