The JAK2 mutation test is a diagnostic procedure used to detect mutations in the JAK2 gene. These mutations are linked to several types of blood disorders.
Myeloproliferative neoplasms (MPNs) like polycythemia vera , essential thrombocythemia (ET), and primary myelofibrosis (PMF) are due to mutation.
The most common mutation tested is JAK2 V617F. Other less common mutations, like JAK2 exon 12 mutations, may also be analyzed.
Jak2 mutation test procedure steps.
The sample is processed to isolate genomic DNA from white blood cells. This step ensures an adequate quality and quantity of DNA for testing.
Several molecular techniques are used to detect the JAK2 mutations:
Be used for more comprehensive analysis, including the detection of rare JAK2 mutations (e.g., exon 12 mutations).
Used in cases where rare mutations or multiple mutations need to be identified.
A highly sensitive method that can detect low levels of the JAK2 V617F mutation in patients with low disease burden.
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