COVID-19 Antibodies Profile (SARS-CoV-2 Serology) in Dubai | 160 AED | DHA Guidelines

Executive Summary & Core Metrics

Executive Summary

Accuracy: 99.9% Diagnostic Sensitivity for IgG/IgM detection via ISO 15189 accredited CLIA processing, validated against clinical datasets.
Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Available daily from 8 AM to 11 PM).
Guidance: Telephonic post-test clinical interpretation by a DHA-licensed General Practitioner, ensuring evidence-based correlation with your vaccination or infection history.
Insurance: Direct billing verification via WhatsApp at +971 54 548 8731.

Test Overview & Methodology

This serology profile detects total antibodies (including IgG and IgM) against SARS-CoV-2 spike and nucleocapsid proteins, differentiating past natural infection from vaccine-induced immunity. It is a cornerstone for population immunity screening and post-vaccination monitoring in the UAE.

Parameter	Our Test (DHA-Accredited)	Closest Alternative (Rapid Lateral Flow)
Precision	99.9% sensitivity, 99.7% specificity (CLIA on automated platform)	~85–93% sensitivity, variable false-negative risk
Methodology	Chemiluminescent Immunoassay (CLIA) – quantitative, clinical-grade	Qualitative immunochromatography, subjective reading
Turnaround	Next-day report (sample by 11 AM)	15–30 minutes (instant but not medically definitive)

Physician Insight & Safety Protocols

Dr. Ajay Singh, DHA License 36234132, advises: “An antibody test reflects your immune system’s memory but is not a standalone immunity passport. I interpret your results alongside vaccination records, symptom history, and clinical risk factors to guide personalised healthcare decisions. If you are immunocompromised, positive results must be interpreted with caution.”

Advisory & Interpretation

This test measures past immune response and is not suitable for diagnosing active COVID-19 infection. Do not use it to replace PCR testing if you are symptomatic or have been recently exposed. Clinical correlation with your medical history and vaccination status is essential.

Safety Exclusion Criteria & Emergency Red Flags

Do not use this test to diagnose acute COVID-19; it is not suitable for active infection detection (seek PCR if symptomatic).
Individuals with known severe needle phobia or haemodynamic instability require in-facility collection.
Red Flags – proceed to ER if you experience: sudden difficulty breathing, persistent chest pain, confusion, or bluish lips/face.

Patient FAQ & Clinical Guidance

1. What does the COVID-19 Antibodies Profile test measure?

A: This quantitative serology panel measures IgG and IgM antibodies against SARS-CoV-2, indicating past infection or vaccination response. It does not diagnose current viral shedding or active infection. It is used for epidemiological surveillance, immunity assessment, and pre-travel screening.

2. How should I prepare for the blood draw?

A: No fasting is required; however, you must complete the mandatory COVID-19 Antibody Form (Form 45) and present a valid Emirates ID. Our phlebotomist ensures cold-chain transport immediately after collection.

3. When can I expect the results and how are they interpreted?

A: Results are delivered the next working day if the sample reaches our lab by 11 AM, with a numerical index and reference ranges. Positive IgG indicates prior exposure; isolated IgM may suggest recent infection; always correlate clinically.

UAE Regulatory & Data Privacy Adherence

Data Privacy Compliance: Your personal health data is processed and stored in full compliance 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 clinical testing safety and patient consent procedures adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability. Your information is used solely for diagnostic purposes and is never shared without your explicit consent.

Clinical & Logistical Metadata

Test Name	COVID-19 Antibodies Profile (SARS-CoV-2 Serology)
Price (AED)	160
Turnaround Time	Next Working Day (Sample by 11 AM)
Sample Type / Matrix	Peripheral Whole Blood (Serum)
Methodology Used	Chemiluminescent Immunoassay (CLIA)
ICD-10-CM Code	Z11.52, U07.1
LOINC Code	94504-7
DHA Facility License & Laboratory Address	License No. 1143 \| Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE \| Corporate Lab: DNA Labs UAE

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