Early Detection of Myeloproliferative Neoplasms
Targeting MPN mutations for personalzied treatment
DNA GTx’s MPN Test is a cutting-edge molecular diagnostic assay designed to accurately identify these clinically relevant mutations. Leveraging highly sensitive real-time PCR technology, the test delivers precise results to support effective patient care.
Who is this Test for?
- Patients with unexplained elevated blood counts
- Suspected cases of Polycythemia Vera (PV), Essential Thrombocythemia (ET), Primary Myelofibrosis (PMF)
- Individuals experiencing symptoms like fatigue, headaches, night sweats, itching, or blood clots
- Patients undergoing treatment monitoring
Mutations Detected
- JAK2
- CALR
- MPL
- CSF3R
Key Benefits
- Provides accurate diagnosis and classification
- Supports personalized, targeted treatment decisions
- Offers valuable prognostic insights
- Enables ongoing treatment monitoring
- High sensitivity and specificity
Turn Around Time
- 3 Days
Do You Need a Doctor’s Request?
Yes. A healthcare provider must request the test and help interpret the results to guide your treatment plan.
How it Works?
Step 1: Blood or bone marrow samples collection
- Peripheral blood or bone marrow sample should be collected
- The sample should be collected in EDTA tubes
Step 2: DNA Extraction
- We carefully extract the DNA from the sample.
- This DNA is what we need to study your genes.
Step 3: PCR Amplification
- Specific regions of DNA are copied millions of times.
- This makes even small mutations easier to detect.
Step 4: Data Analysis
- Our proprietary software (D-KRYPT) helps us understand what the DNA changes mean.
- The results are derived from trusted medical databases.
Step 5: Personalized Patient Report
- You get a clear, easy-to-read report with important findings.
- Your doctor can use this to guide treatment or next steps.
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*All information is handled with strict confidentiality.
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Early detection saves lives
*All information is handled with strict confidentiality.
