LeukoStrat CDx FLT3 Mutation Detection by PCR (INACTIVE as of 02/19/19: Refer to 3001161)
2014683
Ordering Recommendation
Mnemonic
FLT3 CDX
Methodology
Qualitative Polymerase Chain Reaction/Capillary Electrophoresis
Performed
Varies
Reported
3-5 days
New York DOH Approval Status
This test is New York DOH approved.
Submit With Order
ARUP Consult®
Disease Topics
Specimen Required
Patient Preparation
 
Collect
Green (Sodium Heparin). 
Specimen Preparation
Transport 3 mL whole blood. (Min: 1 mL) OR Transport 1 mL bone marrow. (Min: 0.25 mL) Separate specimens must be submitted when multiple tests are ordered. 
Storage/Transport Temperature
Refrigerated. 
Unacceptable Conditions
Specimens in Bone Marrow transport media. Grossly hemolyzed or clotted specimens. 
Remarks
Specimen type required. 
Stability
Ambient: 72 hours; Refrigerated: 1 week; Frozen: Unacceptable 
Reference Interval
Interpretive Data


Note
Hotline History
View Hotline History
Components
Component Test Code*Component Chart NameLOINC
2014684LeukoStrat CDx FLT3 - Specimen Type31208-2
2014685LeukoStrat CDx FLT3 Mutation Detection19146-0
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please view this test within the Laboratory Test Directory found at www.aruplab.com
Aliases

Performed at LabPMM