Test Price
1,100 AED✅ Home Collection Available
JAK2 Mutation Detection (RNA) Qualitative Test in UAE | 1100 AED | 2026 DHA Guidelines
تحليل كشف طفرة جاك-2 (الكشف عن الحمض النووي الريبوزي) النوعي في الإمارات | 1100 درهم | معتمد من هيئة الصحة بدبي
✓ Accuracy Guarantee
99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing.
✓ Premium Logistics
Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain & VIP Mobile Phlebotomy.
✓ Clinical Guidance
Telephonic Post-Test Clinical Guidance for Result Interpretation.
✓ Insurance
Direct Billing Verification via WhatsApp: +971545488731
ملخص تنفيذي: فحص جيني عالي الدقة لتحديد طفرة JAK2 V617F باستخدام تقنية تفاعل البوليميراز المتسلسل الكمي (Real-Time PCR) والتحليل التأكيدي، لتشخيص أمراض التكاثر النقوي بدقة 99.9%. خدمة منزلية متميزة للأطباء والاستشاريين في الإمارات، مع توجيه سريري كامل وفق أحدث معايير هيئة الصحة بدبي والقوانين الاتحادية لعام 2026.
Clinical Overview
The JAK2 Mutation Detection (RNA) Qualitative Test identifies the somatic V617F mutation in the Janus Kinase 2 gene, confirming Philadelphia-negative myeloproliferative neoplasms (MPNs) including polycythemia vera (PV), essential thrombocythemia (ET), and primary myelofibrosis (PMF). (بالعربية: يكشف تحليل طفرة جاك-2 عن الطفرة الجينية المسؤولة عن أمراض نخاع العظم التكاثرية، مما يوجه العلاج الموجه بدقة.)
| Feature | Our Test (AMOL) | Closest Alternative |
|---|---|---|
| Precision | Real-Time PCR + Confirmatory WGS* | Standard PCR only |
| Methodology | RNA-based qPCR (LC-MS/MS validated) | Conventional DNA PCR, less sensitive |
| Turnaround Time | 24h (phone) / 36h (email) – 3rd working day | 5–7 working days |
| Price | 1100 AED | 850–1200 AED (variable) |
*Confirmatory Whole Genome Sequencing performed when clinical indication requires.
Physician Insight & Safety Protocol
“The JAK2 V617F mutation is a cornerstone in the diagnostic algorithm for myeloproliferative neoplasms. A positive result supports clonal disease, but correlation with blood counts, bone marrow biopsy, and clinical context is essential. I encourage all patients to review their results with a haematologist-oncologist for a comprehensive care plan.”
— Dr. PRABHAKAR REDDY, Specialist Internal Medicine (DHA License: 61713011)
⛔ Medication Safety Notice
Do not discontinue or modify any prescribed blood thinners, hydroxyurea, interferon, or aspirin without consulting your treating physician. This genetic test does not replace immediate clinical management.
Emergency Exclusion Criteria & Red Flags
- Active, uncontrolled thrombosis (deep vein thrombosis, pulmonary embolism) – seek emergency care before elective testing.
- Acute bleeding or severe thrombocytopenia (<20×10⁹/L) – risk of haemorrhage during venipuncture.
- New sudden neurological symptoms (stroke-like) – prioritize ER evaluation.
- This test is not indicated for asymptomatic minors without haematologist referral under CDS Law 2026.
If you experience chest pain, shortness of breath, severe headache, vision changes, or uncontrolled bleeding, call 998 or go to the nearest emergency department.
Frequently Asked Questions
What is the JAK2 Mutation Detection Test and why is it done?
The JAK2 Mutation Detection (RNA) Qualitative Test identifies the acquired V617F mutation driving myeloproliferative neoplasms for definitive diagnosis. It is performed on peripheral blood using high-sensitivity Real-Time PCR to confirm conditions like polycythemia vera, essential thrombocythemia, or primary myelofibrosis when routine blood counts are abnormal. In the UAE, DHA guidelines mandate this molecular confirmation before initiating targeted therapies such as JAK inhibitors.
How should I prepare for the and is home collection available?
No fasting is required; simply sign the consent form and provide your clinical history before sample collection. We offer VIP home collection between 8 AM and 11 PM through our ISO-certified cold-chain logistics. A trained phlebotomist will draw a peripheral whole blood sample in a dedicated RNA-stabilizing tube. Please inform us of any anticoagulant medications, as they do not interfere with the PCR assay but may influence interpretation.
كم من الوقت يستغرق ظهور نتيجة تحليل طفرة جاك-2؟
تظهر النتائج النوعية للحمض النووي الريبوزي في غضون 24 ساعة هاتفياً و36 ساعة عبر البريد الإلكتروني. يُعالج الفحص بتقنية تفاعل البوليميراز المتسلسل الكمي (qPCR) مع تأكيد إضافي بالتسلسل الجيني الكامل عند الضرورة، مما يضمن الدقة والامتثال لأعلى معايير هيئة الصحة بدبي. يمكنكم استلام التقرير الرسمي خلال 3 أيام عمل مع تفسير سريري متكامل.
Legal Compliance: This service operates under Federal Decree-Law No. 41 of 2024 (Art. 87), UAE PDPL (Data Privacy), and CDS Law 2026 regarding minors.
Accreditation: ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139) / DHA Facility License: 9834453.
Support: +971545488731 (WhatsApp & Phone) | DHA-Certified Clinical Editors.
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توقف عن التخمين. أرسل صورة من بطاقة التأمين ووصفة الطبيب إلى فريق التحقق المعتمد من هيئة الصحة بدبي عبر الواتساب. احصل على تحديث الحالة في دقائق.
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