Sale!

JAK2 Mutation Detection Panel Exons 12

Original price was: $300.Current price is: $226.

-25%

The JAK2 Mutation Detection Panel Exons 12 is a specialized genetic test that identifies specific mutations in the JAK2 gene, particularly focusing on exon 12 variations. This test plays a crucial role in diagnosing myeloproliferative neoplasms (MPNs) such as polycythemia vera, essential thrombocythemia, and primary myelofibrosis. By detecting these mutations, healthcare providers can confirm diagnoses, guide treatment decisions, and monitor disease progression. The test utilizes advanced Sanger sequencing technology for high accuracy and reliability. Available for only $226 USD, this comprehensive panel provides essential information for patients experiencing unexplained blood cell abnormalities, fatigue, or symptoms suggestive of blood disorders. Early detection through this test enables timely intervention and personalized treatment approaches.

Clinically Validated & Lab Certified

  • ISO-Accredited Laboratory, Ensuring Highest Standards
  • Trusted by Hospitals & Patients —Accredited Testing with Results
  • Direct Healthcare Provider Support + Comprehensive Reporting
Guaranteed Safe Checkout

JAK2 Mutation Detection Panel Exons 12

Comprehensive Genetic Analysis for Blood Disorders

The JAK2 Mutation Detection Panel Exons 12 represents a cutting-edge genetic testing approach specifically designed to identify critical mutations in the Janus Kinase 2 (JAK2) gene. This sophisticated diagnostic tool plays an essential role in the accurate diagnosis and management of various myeloproliferative neoplasms (MPNs), providing healthcare professionals with crucial genetic information to guide treatment decisions and monitor disease progression.

What Does This Test Measure?

The JAK2 Mutation Detection Panel Exons 12 specifically targets and analyzes mutations within exon 12 of the JAK2 gene. This region is particularly significant because mutations in this area can lead to uncontrolled blood cell production, characteristic of several hematological disorders. The test utilizes advanced Sanger sequencing technology to detect:

  • Specific point mutations in JAK2 exon 12
  • Genetic variations associated with polycythemia vera
  • Mutations linked to essential thrombocythemia
  • Genetic markers for primary myelofibrosis
  • Other JAK2-related hematological conditions

Who Should Consider This Test?

This genetic panel is particularly recommended for individuals experiencing symptoms or clinical findings suggestive of myeloproliferative disorders, including:

  • Unexplained elevated red blood cell counts (polycythemia)
  • Persistent high platelet counts (thrombocythemia)
  • Unexplained fatigue and weakness
  • Night sweats and unexplained weight loss
  • Enlarged spleen (splenomegaly)
  • Itching after warm showers or baths (aquagenic pruritus)
  • History of blood clots or thrombosis
  • Abnormal bone marrow findings
  • Family history of blood disorders

Key Benefits of JAK2 Mutation Testing

Undergoing the JAK2 Mutation Detection Panel Exons 12 offers numerous advantages for both patients and healthcare providers:

  • Accurate Diagnosis: Provides definitive genetic confirmation of myeloproliferative neoplasms
  • Personalized Treatment: Enables targeted therapy selection based on genetic profile
  • Disease Monitoring: Helps track disease progression and treatment response
  • Early Intervention: Facilitates timely treatment initiation for better outcomes
  • Family Risk Assessment: Provides information about potential genetic predisposition
  • Comprehensive Analysis: Offers detailed genetic insights beyond standard testing

Understanding Your Test Results

Your JAK2 Mutation Detection Panel results will be carefully interpreted by our expert genetic counselors and hematologists:

  • Positive Result: Indicates the presence of JAK2 exon 12 mutations, confirming diagnosis of associated myeloproliferative disorders
  • Negative Result: Suggests absence of tested JAK2 mutations, though other genetic factors may still be involved
  • Variant of Unknown Significance: Rare genetic variations requiring further clinical correlation
  • Technical Considerations: Results are interpreted in context of clinical presentation and other laboratory findings

Our team provides comprehensive result explanation and guidance on next steps, ensuring you fully understand your genetic profile and its implications for your health management.

Test Pricing and Details

Test Component Details
Test Name JAK2 Mutation Detection Panel Exons 12
Regular Price $300 USD
Discount Price $226 USD
Turnaround Time 7-8 days
Sample Type Bone Marrow/Peripheral Blood
Test Components EDTA Vacutainer (2ml)
Testing Method Sanger Sequencing

Nationwide Testing Availability

We proudly offer the JAK2 Mutation Detection Panel Exons 12 across our extensive network of testing facilities throughout the United States. Our state-of-the-art laboratories are conveniently located in major metropolitan areas including:

  • New York City and surrounding areas
  • Los Angeles and Southern California
  • Chicago and the Midwest region
  • Houston and Texas locations
  • Miami and Florida centers
  • Seattle and Pacific Northwest facilities
  • Boston and New England areas
  • Atlanta and Southeastern locations

Pre-Test Instructions

The JAK2 Mutation Detection Panel Exons 12 requires a Doctor’s prescription for testing. Please note that prescription requirements do not apply for surgery and pregnancy cases or individuals planning to travel abroad. Our team will guide you through the simple preparation process and ensure all necessary documentation is properly handled.

Take Control of Your Health Today

Don’t let uncertainty about potential blood disorders affect your quality of life. The JAK2 Mutation Detection Panel Exons 12 provides the genetic clarity needed for accurate diagnosis and effective treatment planning. Our experienced genetic counselors and hematology specialists are ready to support you through every step of the testing process.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your appointment or learn more about this essential genetic testing panel. Take the first step toward understanding your genetic health and receiving the personalized care you deserve.