Test Price
550 AED✅ Home Collection Available
Immunohistochemistry OCT‑2 Test in UAE – 550 AED
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO‑Accredited Processing.
- Premium Logistics: Secure Medical Courier Solid Tissue Specimen Retrieval – Archival tissues only (FFPE blocks/biopsy slides).
- Clinical Guidance: Free Telephonic Post‑Test Consultation on Result Interpretation.
- Insurance: Direct Billing Verification via WhatsApp at +971 54 548 8731.
Test Overview & Methodology
The Immunohistochemistry (IHC) OCT‑2 Test precisely detects the OCT‑2 (POU2F2) transcription factor in formalin‑fixed paraffin‑embedded (FFPE) tumor tissue, aiding pathologists and oncologists in lymphoma subclassification and targeted therapy selection. This advanced assay combines IHC with fragment length analysis to deliver high‑resolution results within 5–7 business days.
| Feature | Our Test (DHA‑Certified) | Closest Alternative |
|---|---|---|
| Methodology | IHC + Fragment Length Analysis | Standard IHC only |
| Turnaround Time | 5 – 7 days (block/complex) | 10 – 14 days |
| Diagnostic Sensitivity | 99.9% (ISO‑validated) | Not guaranteed |
| Sample Transport | Secure Medical Courier – Room Temperature | Standard postal service |
| Post‑Test Tele‑Consult | Included | Not available |
| Price | 550 AED | 700 – 900 AED |
*Comparison based on publicly available data for regional laboratories. Actual turnaround and service may vary.
Physician Insight & Safety Protocols
"The OCT‑2 immunohistochemistry test is a critical adjunct in differentiating diffuse large B‑cell lymphoma subtypes and guiding targeted treatment strategies. However, results must always be correlated with full histomorphology and clinical context. This biomarker is never interpreted in isolation."
— Mr. Prabhakar Reddy Kalathoor, Specialist Diagnostic Radiology, DHA Registration ID: 61713011
⚠ Advisory Notice
Do not discontinue or alter any prescribed medication without consulting your treating oncologist. Immunohistochemistry results are supplementary; they do not replace clinical judgment or established therapy protocols.
Exclusion Criteria & Emergency Red Flags
- Pregnancy or suspected pregnancy (requires additional risk/benefit assessment).
- Coagulopathy or active bleeding disorder that may complicate biopsy.
- Known allergy to local anaesthetics used in sample collection.
- Seek immediate medical attention if you experience severe pain, swelling, fever, or uncontrolled bleeding at the biopsy site.
Patient FAQ & Clinical Guidance
1. What does the Immunohistochemistry OCT‑2 test detect, and why is it ordered?
The OCT‑2 test identifies the OCT‑2 transcription factor in lymphoma tissue to aid precise subclassification. It helps pathologists and oncologists distinguish between germinal center B‑cell and activated B‑cell subtypes, which directly impacts prognosis and targeted therapy selection. A positive or negative result is never interpreted in isolation; it is integrated with histopathology, immunophenotype, and molecular findings.
2. How is the sample collected and what preparation is needed?
A preserved FFPE tissue block or biopsy in 10% formal‑saline is shipped at room temperature via secure medical courier. No special preparation is required from the patient besides ensuring the biopsy is obtained by a qualified clinician. The laboratory must receive a copy of the original histopathology report, exact biopsy site, and full clinical history to perform accurate correlation. Mobile home phlebotomy is disabled for this archival specimen type.
3. When will I receive my results and how are they protected under UAE law?
Your OCT‑2 immunohistochemistry report is delivered within 5–7 days through a secured, encrypted portal compliant with Federal Decree‑Law No. 45 of 2021 on Personal Data Protection (PDPL). Patient data privacy is maintained under the UAE PDPL, and health information is handled per Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. You will also receive a telephonic guidance call to explain the findings and next steps.
4. Does the test require a biopsy from a hospital or can it be done at home?
Hospital Extraction Only – Sample collection is conducted strictly within an accredited hospital facility; mobile home phlebotomy is disabled for safety. The FFPE tissue block or biopsy slides are then securely couriered to our laboratory. This ensures specimen integrity and adherence to clinical safety protocols under Federal Decree‑Law No. 4 of 2016 on Medical Liability.
UAE Regulatory & Data Privacy Adherence
Full Compliance with UAE Federal Decree‑Law No. 45 of 2021 on Personal Data Protection (PDPL) ensures all patient data is encrypted and processed lawfully. Additionally, Federal Law No. 2 of 2019 concerning the use of information and communication technology in health fields governs the secure handling of electronic health records. Clinical safety and patient consent adhere to Federal Decree‑Law No. 4 of 2016 on Medical Liability. Our laboratory holds ISO 9001:2015 certification (Cert. No. INT/EGQ/2509DA/3139) and operates under DHA Facility License No. 1143.
All clinical information reviewed by Mr. Prabhakar Reddy Kalathoor, Specialist Diagnostic Radiology, DHA Registration ID: 61713011.
Clinical & Logistical Metadata
| Test Name | Immunohistochemistry OCT‑2 Test |
| Price (AED) | 550 AED |
| Turnaround Time | 5–7 Business Days (block/complex) |
| Sample Type / Matrix | Formalin‑Fixed Paraffin‑Embedded (FFPE) Tissue Block or Biopsy Slides (Archival) |
| Methodology Used | Immunohistochemistry (IHC) + Fragment Length Analysis |
| ICD‑10‑CM Code | C83.3, C85.9 |
| LOINC Code | 21757-8 |
| DHA Facility License & Address | License No. 1143, DNA Labs UAE, Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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All reports reviewed by DHA-Certified physicians