JAK2 Mutation PCR Analysis | Lahalak Platform
Advanced molecular PCR test to detect the JAK2 V617F mutation, a cornerstone for diagnosing myeloproliferative disorders like polycythemia vera and essential thrombocythemia.
Scientific name: JAK2 V617F Mutation Analysis by PCR
The JAK2 V617F mutation analysis by polymerase chain reaction (PCR) is a molecular test designed to detect a specific point mutation (valine-phenylalanine substitution at position 617) in the Janus Kinase 2 (JAK2) gene. This mutation is found in the vast majority of patients with polycythemia vera and in a significant proportion of patients with pr...
Service type
Laboratory test (Blood)
Duration
10-15 minutes
Fasting
Fasting is not required
Included Services
- Accurate genetic analysis to detect the V617F mutation in the JAK2 gene using PCR (polymerase chain reaction) technology with sensitive detection methods.
- Consult a specialist in interpreting the results with a hematologist or hematologist-oncologist.
- Personal support services from Halak.
Medical Service Information
Conditions & Notices
- Fasting is not required. A blood sample is drawn into a tube containing an anticoagulant (EDTA) to preserve the white blood cells from which the DNA is extracted.
- No other special preparations are required before taking the sample.
- It is important to inform the doctor about any medications the patient is taking, although most of them do not affect the result of this genetic test.
Medical services you might also like
