Test Price
230 AED✅ Home Collection Available
Epithelial Membrane Antigen (EMA) Immunohistochemistry Test in UAE | 230 AED
Executive Summary & Core Metrics
Core Metrics
The EMA IHC test is performed with 99.9% diagnostic sensitivity using ISO 9001:2015 certified automated immunostaining (clone E29) in our DHA-licensed laboratory (License No. 1143). We offer complimentary temperature-controlled courier retrieval of FFPE blocks from any UAE hospital. Post-test, a 15-minute telephonic clinical correlation session with our diagnostic radiology specialist is included. Direct insurance billing verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The EMA Immunohistochemistry Test detects the epithelial membrane antigen in formalin-fixed, paraffin-embedded (FFPE) tissue biopsies. It aids pathologists in classifying carcinomas, distinguishing mesothelioma from adenocarcinoma, and guiding oncologists toward personalized treatment decisions. Our methodology uses automated IHC with the E29 monoclonal antibody, ensuring consistent staining and high specificity.
| Parameter | Our EMA IHC Test | Alternative UAE Labs |
|---|---|---|
| Precision | 99.9% sensitivity | Variable, often 85–92% |
| Methodology | Automated IHC (clone E29), ISO 9001:2015 quality control | Manual IHC, no independent certification |
| Turnaround | FFPE block: 5 days; large complex tissue: 7 days | 7–10 working days (average) |
| Price | 230 AED | 350–500 AED |
| Logistics | Secure Medical Courier Solid Tissue Specimen Retrieval (hospital collection only) | Patient arranges transport, no mobile service |
Physician Insight & Safety Protocols
"A positive EMA result strongly suggests epithelial differentiation, but clinical and radiological correlation is mandatory. Immunohistochemistry alone should never dictate therapy changes; all findings must be integrated with full histopathological and clinical data. This assay complements, not replaces, a comprehensive diagnostic workup."
— Mr. Prabhakar Reddy Kalathoor, Specialist Diagnostic Radiology | DHA Registration ID: 61713011
Advisory: Clinical Decision Support
Interpretation of EMA IHC results requires correlation with the complete histopathology report, imaging studies, and clinical presentation. Do not base treatment decisions solely on this test. Always request a second review when the result is unexpected or discordant with other findings.
Exclusion Criteria & ER Red Flags
- Inadequate biopsy specimen (crush artifact, extensive necrosis).
- Improperly fixed tissue (fixation time <6 hours or >72 hours in 10% formalin).
- For surgical pathology second opinion, block must be accompanied by original histopathology report.
- Seek emergency care if you experience severe pain, bleeding, or signs of infection at the biopsy site after collection.
Patient FAQ & Clinical Guidance
1. What is the purpose of the EMA IHC test?
This test identifies epithelial tumors and differentiates carcinomas from mesothelioma by detecting the epithelial membrane antigen in tissue biopsies. It helps pathologists classify cancers and guides targeted therapy decisions.
2. How should I prepare for specimen collection?
The tissue biopsy is collected by a surgeon during a biopsy procedure. You need only provide your clinical history and any previous histopathology reports. No special preparation is required from your side.
3. Can the test be done with home collection?
No, the EMA IHC test uses FFPE tissue blocks that must be retrieved from the hospital where the biopsy was performed. We arrange a secure medical courier for specimen pickup. Home collection is not available for this test type.
4. How long does it take to get results?
Results from FFPE blocks are available within 5 working days. Complex or large tissue samples may require up to 7 days. You will receive a telephonic clinical correlation session within 15 minutes after the report is ready.
5. Is the test covered by insurance?
We offer direct insurance billing verification via WhatsApp at +971 54 548 8731. Coverage depends on your individual policy. Please contact us for pre-approval assistance.
UAE Regulatory & Data Privacy Adherence
Compliance Framework
All laboratory practices comply with Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. Clinical testing and patient consent adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability. ISO 9001:2015 certified (Cert: INT/EGQ/2509DA/3139).
Clinical & Logistical Metadata
| Test Name | Epithelial Membrane Antigen (EMA) Immunohistochemistry |
| Price (AED) | 230 AED |
| Turnaround Time | 5–7 working days |
| Sample Type / Matrix | Archival Tissue Specimen – Formalin-fixed, paraffin-embedded (FFPE) tissue blocks or slides. Hospital extraction only; mobile home phlebotomy is disabled. Secure Medical Courier Solid Tissue Specimen Retrieval. |
| Methodology Used | Automated Immunohistochemistry (IHC) with anti-EMA antibody (clone E29), ISO 9001:2015 quality control |
| ICD-10-CM Code | C80.1 (Malignant neoplasm, unspecified) |
| LOINC Code | 62806-2 (Epithelial membrane antigen [Interpretation] in Tissue by Immunoperoxidase) |
| DHA Facility License & Laboratory Address | License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians