JAK 2 EXON 12 15

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JAK2 Exon 12 and 15 Mutation Detection / EDTA Blood is a molecular test that identifies mutations in the JAK2 gene, which are associated with myeloproliferative disorders such as polycythemia vera, essential thrombocythemia, and primary myelofibrosis. Detection of these mutations helps confirm diagnosis, guide prognosis, and monitor therapy. Metropolis Healthcare performs this test using sensitive PCR-based molecular techniques to ensure accurate and reliable detection of JAK2 gene alterations

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Price: Rs. 7,500.00

Sample Type: EDTA Whole Blood

Fasting Not Required


Notes: J8360

Frequently Asked Questions (FAQ's):

What does this test detect?
It identifies mutations in JAK2 exons 12 and 15 linked to myeloproliferative disorders.

Who should undergo this test?
Patients with elevated blood counts, unexplained thrombosis, or suspected myeloproliferative neoplasms.

Is fasting required?
No fasting is required.

What sample is needed?
An EDTA blood sample for molecular analysis.

How does Metropolis Healthcare perform this test?
Using PCR and advanced molecular techniques to detect JAK2 gene mutations accurately.

Can this test guide treatment decisions?
Yes, mutation status helps in diagnosis, prognosis, and therapy planning for myeloproliferative disorders.

Are additional tests recommended?
Metropolis Healthcare may suggest complete blood count, bone marrow studies, or other genetic tests for comprehensive assessment.

How long does it take to get results?
Results are typically available within 5–10 days depending on sample processing and analysis

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