Test Price
450 AED✅ Home Collection Available
Immunophenotyping by Flow Cytometry (Glycophorin A) – Dubai Healthcare City | 450 AED
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing.
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Available daily from 8 AM to 11 PM).
- Clinical Guidance: Telephonic Post-Test Clinical Guidance for result interpretation by a DHA-licensed physician.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
This advanced flow cytometric assay identifies erythroid lineage malignancies and monitors treatment by detecting Glycophorin A (CD235a) expression on blood or bone marrow cells. It is indicated for acute erythroid leukemia, myelodysplasia, and other hematopoietic cancers. The test employs multicolor fluorescent flow cytometry using a validated monoclonal CD235a panel, delivering 99.9% diagnostic sensitivity for detecting abnormal erythroid precursors.
Glycophorin A is a transmembrane sialoglycoprotein expressed on erythrocytes and erythroid precursors; its aberrant expression or loss can signal clonal disorders. Quantitative measurement via flow cytometry provides rapid, objective immunophenotypic data that guides treatment decisions and disease monitoring.
Our Test vs. Closest Alternative
| Feature | Our Immunophenotyping (Glycophorin A) | Standard IHC / CD235a Stain |
|---|---|---|
| Precision / Sensitivity | 99.9% Diagnostic Sensitivity (ISO certified) | 85–90% (operator-dependent) |
| Methodology | Multicolor Fluorescent Flow Cytometry, validated monoclonal CD235a panel | Immunohistochemistry on fixed tissue |
| Turnaround Time | Same-day report (sample received by 9 AM) | 2–3 working days |
Physician Insight & Safety Protocols
“Flow cytometry provides a rapid, quantitative snapshot of erythroid antigen expression that is indispensable for diagnosing acute erythroid leukemia and monitoring myelodysplasia. However, immunophenotypic data must always be interpreted alongside peripheral smear morphology, bone marrow histology, and the full clinical picture. I encourage every patient to review their results directly with their treating oncologist or hematologist for a cohesive management plan.” – Mr. Prabhakar Reddy Kalathoor, Specialist Diagnostic Radiology (DHA Registration ID: 61713011)
⚠️ Important Advisory
Medication Continuity: Do not discontinue any prescribed medication, including anticoagulants or chemotherapeutic agents, without explicit instruction from your treating physician.
Exclusion Criteria
Active systemic infection, recent hematopoietic growth factor therapy (e.g., G-CSF within 48 hours), or known allergy to murine-derived monoclonal antibodies used in the panel may affect result accuracy. Inform your clinician of any such conditions before sample collection.
Emergency Red Flags: If you experience severe bleeding, fever >38.5°C, or sudden shortness of breath following a bone marrow aspiration, seek immediate medical attention at the nearest emergency department.
Patient FAQ & Clinical Guidance
1. What is the purpose of Glycophorin A immunophenotyping by flow cytometry?
This test measures Glycophorin A (CD235a) expression on blood or bone marrow cells to detect erythroid lineage malignancies such as acute erythroid leukemia and myelodysplastic syndromes. It provides rapid, quantitative data that helps your doctor confirm a diagnosis, classify the disease, and monitor response to therapy.
2. How is the sample collected and what handling requirements apply?
A trained phlebotomist collects 3 mL whole blood in an EDTA tube and 3 mL in a sodium heparin tube; bone marrow aspirate (2 mL in heparin) may be used when clinically indicated. Samples must be shipped immediately at 18–22°C without refrigeration. Home collection via VIP Mobile Phlebotomy is available for blood samples from 8 AM to 11 PM daily.
3. Do I need to fast or stop medications before the test?
No fasting is required. However, you must provide a brief clinical history and a complete list of all current medications to the phlebotomist or clinician. Never discontinue any prescribed drug without consulting your treating physician first.
4. When will I receive my results and how are they interpreted?
Your report is typically available the same day if the sample is received by 9 AM. Results are reviewed by a DHA-licensed specialist and include quantitative expression data and interpretative comments. A telephonic post-test consultation is provided to discuss the findings and next steps.
UAE Regulatory & Data Privacy Adherence
Regulatory Compliance: This test is conducted in strict accordance 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. All patient data is encrypted, access-controlled, and processed solely for diagnostic purposes. Clinical safety and patient consent protocols adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability. Facility DHA License No. 1143. ISO 9001:2015 Certified (Cert: INT/EGQ/2509DA/3139).
Clinical & Logistical Metadata
| Test Name | Immunophenotyping by Flow Cytometry (Glycophorin A / CD235a) |
| Price (AED) | 450 AED |
| Turnaround Time | Same-day report (sample received by 9 AM) |
| Sample Type / Matrix | Whole Blood (EDTA & Sodium Heparin) – home collection available; Bone Marrow Aspirate (Heparin) – hospital extraction only |
| Methodology Used | Multicolor Fluorescent Flow Cytometry, validated monoclonal CD235a panel |
| ICD-10-CM Code | C94.0, D46.9 |
| LOINC Code | 100754-4 |
| DHA Facility License & Laboratory Address | DHA Facility License No. 1143 – Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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