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Test Price

600 AED

✅ Home Collection Available

Pan Enteric Bacteria (RNA Detection) Qualitative Test in Dubai, UAE

Executive Summary & Core Metrics

  • Diagnostic Accuracy: 99.9% sensitivity via validated RNA detection with Real-Time PCR (qPCR) and Whole Genome Sequencing (WGS), certified under ISO 9001:2015 (Certificate: INT/EGQ/2509DA/3139).
  • Premium Logistics: VIP mobile phlebotomy with temperature-controlled cold-chain home collection available daily from 8 AM to 11 PM. Hospital-grade specimen handling ensures sample integrity from bedside to laboratory.
  • Clinical Guidance: Post-result telephonic consultation with a licensed physician to interpret findings and recommend next steps.
  • Insurance Facilitation: Direct insurance coverage verification via WhatsApp at +971 54 548 8731 before sample collection.

Test Overview & Methodology

The Pan Enteric Bacteria RNA Detection test is a qualitative molecular diagnostic assay designed to identify a broad spectrum of enteric bacterial pathogens from whole blood, rectal swabs, food matrices, and environmental water samples. Using a dual-platform approach combining Real-Time PCR (qPCR) with Whole Genome Sequencing (WGS), the assay delivers high-specificity identification of viable, metabolically active organisms. This method significantly reduces time-to-diagnosis compared with conventional stool culture or antigen-based techniques, enabling earlier clinical intervention in suspected gastroenteritis, foodborne outbreaks, or environmental contamination events.

Feature Our Test Closest Alternative
Precision 99.9% sensitivity via RNA + WGS Standard culture (lower sensitivity, 48–72 h)
Methodology Real-Time PCR (qPCR) + Whole Genome Sequencing Conventional PCR or stool antigen tests
Speed Preliminary phone result: 24 h | Final report: 36 h 3–5 working days

Physician Insight & Safety Protocols

“RNA detection via qPCR combined with whole genome sequencing provides an exceptionally rapid and precise window into active enteric infections. However, molecular findings must always be interpreted within the full clinical context, including symptom chronology, travel history, and prior antibiotic exposure. Laboratory data alone should never drive treatment decisions; a comprehensive patient assessment remains indispensable.”

— Dr. Ajay Singh, General Practitioner, DHA Registration ID: 36234132

Advisory Considerations Before Testing

Pre-Test Guidance

  • Inform your physician if you have taken antibiotics within the past 72 hours, as recent antimicrobial use may reduce bacterial RNA detectability.
  • Provide a complete history of gastrointestinal symptoms, recent travel, and known food or water exposures to assist in result interpretation.
  • No fasting is required for blood collection; specific instructions will be provided for stool or rectal swab samples.

Exclusion Criteria & Clinical Red Flags

Do Not Proceed With Home Collection If Any of the Following Are Present

  • Suspected acute surgical abdomen (e.g., perforation, obstruction, or peritonitis).
  • High fever exceeding 39°C persisting despite antipyretics, or clinical signs of severe dehydration.
  • Altered mental status, severe immunocompromise (recent chemotherapy, post-transplant), or haemodynamic instability.
  • Visible blood in stool or severe abdominal rigidity requiring emergency evaluation.

If you experience any of the above, seek emergency medical care immediately. This test is not a substitute for urgent clinical assessment.

Patient FAQ & Clinical Guidance

1. What does the test detect and why is RNA used instead of DNA?

This qualitative assay detects a broad panel of enteric bacterial pathogens from blood, stool, food, or water samples. RNA targeting identifies viable, actively metabolising organisms, offering earlier and more specific detection compared with DNA-based methods or traditional culture. This approach reduces false positives from non-viable organisms and accelerates time to accurate diagnosis.

2. What preparation is required before sample collection?

Sign the informed consent form and provide your complete clinical history, including recent gastrointestinal symptoms, travel, and known exposures. No fasting is necessary for a blood draw. For stool or rectal swab specimens, the phlebotomist will supply detailed collection instructions. Inform the team if you have taken antibiotics in the last 72 hours, as this may affect sensitivity.

3. How quickly will I receive my results and how are they delivered?

A preliminary phone result is available within 24 hours of sample receipt. The final verified electronic report is emailed within 36 hours. Urgent cases can be prioritised by requesting express handling via WhatsApp at +971 54 548 8731. Our VIP mobile phlebotomy service operates daily from 8 AM to 11 PM, using cold-chain transport to the ISO-certified laboratory.

4. Can I use my health insurance to cover the test cost?

Yes. Direct insurance coverage verification and billing can be arranged through our WhatsApp service at +971 54 548 8731 before sample collection. Please have your insurance policy details ready for a seamless pre-authorisation process. The test price is 600 AED.

UAE Regulatory & Data Privacy Adherence

DNA Labs UAE operates under the regulatory oversight of the Dubai Health Authority (DHA Facility License Number: 1143) and complies fully 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 are conducted in accordance with Federal Decree-Law No. 4 of 2016 on Medical Liability. Patient data is encrypted, access-controlled, and never shared with third parties without explicit written consent. Our laboratory holds ISO 9001:2015 certification (Certificate: INT/EGQ/2509DA/3139) and follows stringent quality management protocols for every stage of sample handling, analysis, and reporting.

Clinical & Logistical Metadata

Test Name Pan Enteric Bacteria (RNA Detection) Qualitative Test
Price (AED) 600
Turnaround Time 24 hours (preliminary phone result) / 36 hours (final electronic report)
Sample Type / Matrix Whole Blood, Rectal Swab, Food, Environmental Water
Methodology Used Real-Time PCR (qPCR) + Whole Genome Sequencing (WGS)
ICD-10-CM Code A04.9, A09
LOINC Code 80618-7
DHA Facility License & Laboratory Address DHA Facility License Number: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE

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