Test Price
450 AED✅ Home Collection Available
CD1a Immunophenotyping by Flow Cytometry – 450 AED
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 accredited processing, eliminating false negatives in CD1a+ cell detection.
- Hospital Collection Only: Sample collection is conducted strictly within an accredited hospital facility; mobile home phlebotomy is disabled for safety. Bone marrow aspirate or peripheral blood must be collected under clinical supervision.
- Clinical Guidance: Complimentary Telephonic Post-Test Clinical Guidance by DHA-licensed physicians to interpret your CD1a results in the context of your medical history.
- Insurance: Direct Billing Verification via WhatsApp at +971 54 548 8731 – compliant with UAE PDPL and Federal Law No. 2 of 2019 on Health Data.
Test Overview & Methodology
CD1a Immunophenotyping by Flow Cytometry is a specialised assay that uses fluorescent-labelled antibodies to quantify the CD1a protein on the surface of blood or bone marrow cells, a critical biomarker for Langerhans cell histiocytosis and T-lymphoblastic leukemia/lymphoma. In the UAE, our same-day reporting and ISO‑certified protocol ensure haematologists and oncologists receive clinically actionable results within hours.
| Feature | Our Test – CD1a Flow Cytometry | Closest Alternative |
|---|---|---|
| Detection Precision | High-resolution 10‑colour flow cytometry with CD1a‑PE conjugate | Conventional 4‑colour panel; may miss dim CD1a expression |
| Methodology | Fluorescence‑activated cell sorting (FACS) on BD FACSCanto™ II, ISO‑standardised | Generic flow cytometry without ISO validation |
| Turnaround Time | Same‑day (sample by 9 AM → report by evening) | 48–72 hours |
| Sample Collection | Hospital extraction only (bone marrow/blood at DHA‑licensed facility) | Often unavailable or non‑certified |
Physician Insight & Safety Protocols
“As a diagnostic radiologist with deep experience in oncology biomarkers, I understand that awaiting CD1a immunophenotyping can be unsettling. A positive CD1a result is a pivotal clue in differentiating aggressive T‑cell malignancies from reactive conditions; our laboratory ensures rigorous pre‑analytical quality so your clinical decision rests on evidence. Please remember that flow cytometry results complement histopathology and your complete clinical picture.”
— Mr. Prabhakar Reddy Kalathoor, Specialist Diagnostic Radiology, DHA Registration ID: 61713011
Advisory: Medication Precautions
⚠ Important Medication Notice
Do not discontinue any prescribed medication, including corticosteroids or chemotherapy, without explicit instruction from your treating physician. Altered immune status may affect CD1a expression; always consult your doctor before changing your regimen.
Exclusion Criteria & Emergency Red Flags
- Exclusion: Patients with active systemic infection or within 2 weeks of high‑dose immunosuppressive therapy (sample cell viability may be compromised).
- Exclusion: Inadequate sample volume (<2 mL whole blood or <1 mL bone marrow) or incorrect anticoagulant (must be EDTA plus sodium heparin – see pre‑test guidance).
- Red Flag – Seek Emergency Care: If you experience sudden high fever (>38.5 °C), severe unexplained bleeding, or acute neurological changes (confusion, loss of consciousness) while awaiting results, go to the nearest emergency department immediately.
Patient FAQ & Clinical Guidance
1. What is CD1a immunophenotyping used for in oncology?
Snippet‑optimised answer: CD1a immunophenotyping by flow cytometry identifies cells bearing the CD1a surface protein, an essential diagnostic marker for Langerhans cell histiocytosis (LCH) and T‑cell acute lymphoblastic leukemia (T‑ALL), aiding oncologists and hematologists in precise subclassification of aggressive blood disorders.
2. How should I prepare for the CD1a flow cytometry blood and bone marrow collection?
Snippet‑optimised answer: Preparation involves providing a brief clinical history and ensuring sample tubes are mixed immediately after collection; a lavender‑top EDTA tube and a green‑top sodium heparin tube are required, and the specimen must be shipped at 18–22 °C without refrigeration to preserve cell viability. Collection occurs only at the hospital facility.
3. Is 450 AED a competitive price for this in the UAE, and will insurance cover it?
Snippet‑optimised answer: At 450 AED, our CD1a immunophenotyping is priced competitively within DHA‑regulated rates and includes ISO‑certified accuracy, same‑day reporting, and hospital protocol oversight; direct insurance billing verification is available via WhatsApp at +971 54 548 8731, conforming to UAE PDPL and Federal Law No. 2 of 2019.
UAE Regulatory & Data Privacy Adherence
Compliance & Accreditation
DNA Labs UAE operates under DHA Facility License 1143 (Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE). Our laboratory is certified ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139). We adhere 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. Patient data is encrypted and all personnel are DHA‑licensed. For consent and clinical safety, we follow Federal Decree-Law No. 4 of 2016 on Medical Liability.
Clinical & Logistical Metadata
| Test Name | CD1a Immunophenotyping |
| Price (AED) | 450 |
| Turnaround Time | Same‑day (sample by 9 AM, report by evening) |
| Sample Type / Matrix | Hospital Extraction Only – Bone Marrow Aspirate or Peripheral Blood (collection at hospital facility) |
| Methodology Used | Fluorescence‑Activated Cell Sorting (FACS) – BD FACSCanto™ II |
| ICD-10-CM Code | C96.0 (Langerhans cell histiocytosis) |
| LOINC Code | 53926-4 (CD1a [Presence] in Blood or Bone Marrow by Flow cytometry) |
| DHA Facility License & Laboratory Address | License: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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