JAK2 V617F MUTATION DETECTION BY RT PCR / EDTA BLOOD

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NABL Cap Accredited 
The JAK2 V617F Mutation Detection by RT-PCR / EDTA Blood test identifies the presence of the JAK2 V617F mutation, a key genetic marker associated with myeloproliferative neoplasms (MPNs). Metropolis Healthcare uses sensitive RT-PCR technology to provide accurate and early detection. This test helps clinicians diagnose conditions such as polycythemia vera, essential thrombocythemia, and primary myelofibrosis. An EDTA blood sample ensures precise and reliable genetic analysis.

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Price: Rs. 7,299.00

Sample Type: EDTA BLOOD

Fasting Not Required


Notes: J0004

Frequently Asked Questions (FAQ's):

What does the JAK2 V617F Mutation Detection test include?
This test analyzes EDTA blood to detect the JAK2 V617F mutation associated with various myeloproliferative disorders.

How does Metropolis Healthcare perform this test?
Metropolis Healthcare uses validated RT-PCR protocols under strict quality control to ensure highly sensitive and specific mutation detection.

Who should take this test?
Individuals with elevated blood counts, suspected MPNs, or unexplained thrombotic events may be advised to undergo this test.

What sample type is required?
An EDTA blood sample is required for accurate and reliable genetic testing.

Why is detecting the JAK2 V617F mutation important?
It aids in confirming the diagnosis of MPNs, guiding treatment decisions, and assessing disease prognosis.

How reliable are results from Metropolis Healthcare?
Metropolis Healthcare ensures high accuracy through advanced RT-PCR methods, stringent quality control, and expert interpretation.

Is any preparation needed before the test?
No fasting or special preparation is required; patients should follow any physician instructions provided.

How soon are results available?
Turnaround time may vary, but Metropolis Healthcare typically provides prompt results to support early diagnosis and management.

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