JAK2 V617F Mutation in Kadi
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JAK2 V617F mutation by PCR1
FAQ
Why should I book JAK2 V617F Mutation Test with Sterling Accuris Diagnostics?
Sterling Accuris Diagnostics is at the forefront of pathology services in India, with international quality standards. Our NABL-accredited laboratory specializes in providing quick and reliable primary diagnosis support for hospitals, physicians and other healthcare facilities across the country. We even offer home collections for a JAK2 V617F Mutation Test in Kadi .
It is extremely convenient to book a JAK2 V617F Mutation Test with us that would give you accurate and precise results at a great price.
How long does it take to get the results of a JAK2 mutation test?
It is dependent upon the laboratory doing the test. Results are often available within a few weeks.
Should a JAK2 mutation test be repeated?
If the test is negative and the doctor thinks the mutation might have been missed, the doctor may repeat it.
Can this test be completed in the doctor's office?
Testing for JAK2 mutations must be done in a lab that conducts molecular testing.
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For us, precision care, safe sample collection, timely delivery of reports, and precise reporting of patient results while adhering to health and safety precautions are the cornerstone of our success.
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Yes. We do provide home collection services at your doorstep.
Please go ahead and book your visit today from our top menu options in this website / chat or do call us on 812 813 0000.
How long does it take to receive test results?
Though most tests are completed and reported within about 24 hours of receiving the sample for testing, certain tests take several days to weeks.
Your soft copy will be sent on registered email id and Whatsapp. Also, you will receive SMS with link to download your report. Also, your report is available on our website / app.
To know the status of the report, you can call our customer care team on 812 813 0000.
Is there any preparation or precautions for patient before tests or body checkup?
Fasting maybe required in case of a few tests to ensure accurate results.
In general, it is also advisable to abstain from alcohol and heavy diet at least for 24 hours before any health test. You can see the requirement for each test on the product page on our website / app.
JAK2 V617F Mutation Test in Kadi
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Sterling Accuris Diagnostics offers the JAK2 V617F Mutation Test in Kadi to diagnose myeloproliferative neoplasms (MPNs) and bone marrow conditions.
Overview of JAK2 V617F Mutation Test
The basic JAK2 test is called JAK2 V617F, following a mutation in the JAK2 gene at a specific location in the genome. The Janus Kinase 2 gene, abbreviated JAK2, gives cells the information they need to produce the JAK2 protein. This protein encourages cell division and proliferation, and it is especially important for regulating the generation of blood cells in the bone marrow. One DNA nucleotide base pair is altered by the JAK2 V617F mutation, which is acquired rather than inherited. This type of mutation, known as a point mutation, causes the amino acid valine to be switched for phenylalanine in JAK2. This amino acid alteration causes the JAK2 protein to become permanently "on," which triggers uncontrolled blood cell formation. There are known bone marrow diseases caused by JAK2 mutations.
For accurate and precise test results head on to Sterling Accuris Diagnostics for the JAK2 V617F Mutation Test in Kadi
Why and when is the JAK2 V617F Mutation Test done?
The JAK2 mutation test may be used to help identify bone marrow conditions that result in the overproduction of blood cells.
When a patient's hemoglobin, hematocrit, red blood cell, and platelet counts are significantly elevated and the doctor suspects that the patient may have an MPN, particularly polycythemia vera (PV), essential thrombocythemia (ET), or primary myelofibrosis (PMF), the JAK2 mutation test is frequently requested as a follow-up test.
However, a doctor may suspect an MPN and request testing if a patient has, for instance:
- An enlarged liver or spleen (splenomegaly)
- A blood clot in an artery or vein
- A heart attack or transient ischemic attack
- Bleeding
- Headaches
- Dizziness
- Vision problems
- Numbness
- Gout
- Kidney stones
- Itchiness
JAK2 V617F Mutation Test: Main Highlights
- Instructions: No specific preparation is required.
- Recommended Age: Any age group.
- Sample type for test: Blood EDTA.
Understanding how to interpret JAK2 V617F Mutation Test Reports
If the JAK2 V617F mutation test is positive and there are further clinical signs it is likely that the test person has an MPN.
A person is most likely to have polycythemia vera if they have a negative JAK2 V617F test but a positive JAK2 exon 12 mutation test or another non-V617F mutation test, along with accompanying clinical indications.
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