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BCR/ABL1 qRT PCR

Test ID: M BCR ABL CPT Code: 81206

Expected Turnaround Time
7 days
Stated turn-around-times (TATs) are for clinical use only and subject to change based on biopharma protocol requirements. Final TATs will be specified in the biopharma study contract.

Clinical Information
Quantitative reverse transcriptase polymerase chain reaction (qRT-PCR) for the detection of the major BCR::ABL fusion gene transcript p210 (e13/e14a2) in patients with a Philadelphia (t[(9;22)(q34;q11.2)]) positive leukemia. The BCR::ABL major translocation is found in >99% of CML patients. Results for the major BCR::ABL fusion gene transcripts are reported on the international scale (IS).

Requisition Forms

Specimen Requirements


Specimen Requirements
  • Whole Blood: 10 mL (minimum 5mL), EDTA preferred (NaHep accepted)
  • Bone Marrow Aspirate: 3 mL (minimum 1 mL), EDTA preferred (NaHep accepted)

Specimen Stability

Specimen must be received by MPLN within 48 hours of collection.

 


Storage Requirements

2-8°C


Shipping Recommendations

REFRIGERATED, Protect from extreme temperature with ice pack. Separate ice pack from specimen.


Specimen Rejection Criteria

Specimen >48 hours old; Specimen clotted; Specimen stored or shipped at incorrect temperature; Specimen in incorrect anticoagulant; Insufficient specimen volume; Isolated RNA of suboptimal quantity and/or quality


Test Details


Synonyms

Philadelphia Chromosome; major t(9;22) e13/e14(p210)


Keywords
Leukemia, Molecular Diagnostics, Oncology, Acute Lymphoblastic Leukemia (ALL), Chronic Myelogenous Leukemia (CML), Quantitative PCR, Genomics

Test Method
Quantitative reverse transcriptase polymerase chain reaction (qRT-PCR)

Methodology Category
Molecular

Regulatory Status
RUO

Special Considerations
  • Frozen blood samples are NOT accepted.
  • Please notify MPLN if shipment is to arrive after 1 p.m. Friday or Saturday.

Associations

Chronic myelogenous leukemia (CML), Acute lymphoblastic leukemia (ALL), Allogeneic bone marrow transplantation, Minimal residual disease (MRD), Molecular remission, Tyrosine Kinase Inhibitors