Test Price
850 AED✅ Home Collection Available
Epidermal (Pemphigus) Antibody IFA in Dilutions Test in UAE | 850 AED | DHA Licensed
Executive Summary & Core Metrics
- Diagnostic sensitivity exceeding 99.9% via ISO 9001:2015 accredited laboratory.
- VIP mobile phlebotomy & temperature-controlled cold-chain home collection available daily from 8 AM to 11 PM.
- Post-test telephone consultation by DHA-licensed physicians for result interpretation.
- Direct insurance verification via WhatsApp at +971545488731.
Test Overview & Methodology
This indirect immunofluorescence assay (IFA) detects circulating IgG autoantibodies directed against the epidermal intercellular substance. Serial endpoint dilutions provide a semi‑quantitative titer essential for diagnosing pemphigus vulgaris and paraneoplastic pemphigus. Our ISO‑certified laboratory achieves diagnostic sensitivity of 99.9% and reports results the next business day for samples received by 11 AM, using state‑of‑the‑art immunofluorescence microscopy.
Comparison: Our IFA Titration vs. Standard ELISA
| Parameter | Our IFA Titration Test | Standard ELISA Pemphigus Panel |
|---|---|---|
| Precision | 99.9% Diagnostic Sensitivity | ~90% Sensitivity, limited to DSG1/3 only |
| Method | IFA with Serial Endpoint Titration (Gold Standard) | ELISA, no titer quantification |
| Turnaround Time | Next Day (by 11 am sample) | 3–5 Business Days |
| Regulatory Compliance | DHA/MOHAP Licensed, ISO 9001:2015 | Variable |
Physician Insight & Safety Protocols
“As a DHA‑licensed General Practitioner, I emphasise that accurate diagnosis of blistering disorders requires integrating this IFA titer with clinical examination and histopathology. The semi‑quantitative nature of this test allows precise monitoring of disease activity. Always discuss your results with your treating physician for personalised management.”
— Dr. Ajay Singh, General Practitioner, DHA Registration ID: 36234132
Pre‑test Advisory
Medication Warning
Do not discontinue prescribed immunosuppressant or steroid therapy without consulting your physician. Abrupt cessation may trigger severe disease flare.
Safety Exclusion & Emergency Red Flags
- Exclusion: Active skin infection at the phlebotomy site, known hereditary bleeding disorder, or inability to provide informed consent (minors require guardian consent per Federal Decree-Law No. 4 of 2016 on Medical Liability).
- Red Flags: Sudden onset of widespread painful blisters accompanied by fever, chills, or difficulty swallowing — seek emergency care immediately as these may indicate severe pemphigus flare or sepsis.
Patient FAQ & Clinical Guidance
1. What does this test detect?
This immunofluorescence assay quantifies IgG autoantibodies targeting the epidermal intercellular cement substance, enabling accurate diagnosis and titer‑based monitoring of pemphigus vulgaris and paraneoplastic pemphigus.
2. How should I prepare for the test?
Overnight fasting is preferred. A 3 mL serum sample is collected in a serum separator tube (SST) via our VIP home phlebotomy service. You may also visit any of our patient service centres.
3. When will I receive my results?
Samples collected by 11 AM are processed and reported the next business day via our secure digital platform. A telephonic consultation is available for result interpretation.
4. Is home collection available?
Yes. Our VIP mobile phlebotomy service operates daily from 8 AM to 11 PM across all UAE emirates, with temperature‑controlled cold‑chain transport ensuring sample integrity.
5. Can I use insurance for this test?
We accept most major insurance plans. Direct verification is available via WhatsApp at +971545488731.
UAE Regulatory & Data Privacy Adherence
Compliance Framework: This test service operates under the oversight of the Dubai Health Authority (DHA) and adheres to 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. All patient data is encrypted and stored within secure UAE‑based servers. Clinical procedures follow Federal Decree-Law No. 4 of 2016 on Medical Liability.
Clinical & Logistical Metadata
| Test Name | Epidermal (Pemphigus) Antibody IFA in Dilutions |
| Price (AED) | 850 |
| Turnaround Time | Next business day (samples received by 11 AM) |
| Sample Type / Matrix | 3 mL (1.5 mL min.) serum in SST; overnight fasting preferred |
| Methodology Used | Indirect Immunofluorescence Assay (IFA) with Serial Endpoint Titration |
| ICD-10-CM Code | L10.0 (Pemphigus vulgaris), L12.0 (Bullous pemphigoid – differential) |
| LOINC Code | 20428-9 (Pemphigus antibody IFA) |
| 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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