Test Price
350 AED✅ Home Collection Available
RNA Extraction from Solid Tissue in Dubai | 350 AED | DHA Certified Molecular Genetics Test
Executive Summary & Core Metrics
99.9% Diagnostic Sensitivity | ISO-Certified Cold-Chain Logistics | Post-Test Clinical Guidance
- Accuracy Guarantee: 99.9% diagnostic sensitivity achieved through ISO 9001:2015 accredited RNA extraction protocols, verified by NanoDrop spectrophotometry and RNA integrity (RIN) scoring. Ensures reliable downstream molecular testing including RT-qPCR, microarray analysis, and next-generation sequencing (NGS).
- Hospital Extraction Only: Sample collection is conducted strictly within an accredited hospital facility; mobile home phlebotomy is disabled for safety. GPS-tracked courier service ensures specimen integrity from hospital to laboratory under controlled 2–8°C cold-chain transport.
- Clinical Guidance: Complimentary telephonic post-test interpretation by DHA-licensed Consultant Medical Genetics. Detailed clinical correlation report provided with every result to support informed therapeutic decisions.
- Insurance: Direct billing verification via WhatsApp at +971 54 548 8731. Accepting major UAE insurers with real-time eligibility checks.
Test Overview & Methodology
This test isolates high-integrity total RNA from solid tissue specimens (biopsy or surgical resection) for molecular diagnostics, gene expression profiling, and personalized therapeutic decision-making. The extraction process follows DHA-endorsed ISO 9001:2015 protocols using silica membrane spin column technology with DNase I treatment to remove genomic DNA contamination. Each sample undergoes quality control assessment with RIN value reporting to confirm RNA suitability for downstream applications including RT-qPCR, microarrays, and next-generation sequencing.
| Parameter | DNA Labs UAE RNA Extraction | Conventional Laboratory Alternative |
|---|---|---|
| Diagnostic Sensitivity | 99.9% (NanoDrop/QC-verified with RIN scoring) | Variable, typically 85–90% without standardized QC |
| Extraction Method | Silica membrane spin columns with DNase I treatment (ISO 9001:2015 certified) | Manual phenol‑chloroform extraction with higher contamination risk |
| Turnaround Time | 5–7 business days from sample receipt | 10–14 business days typical |
| Collection Protocol | Hospital extraction only; specimen placed in RNA stabilizer immediately after resection with expedited cold-chain transport | Limited or unavailable for tissue specimens; higher risk of RNA degradation |
Physician Insight & Safety Protocols
"RNA integrity is the cornerstone of accurate molecular diagnostics. As a Consultant Medical Genetics, I emphasize that the quality of extracted RNA directly determines the reliability of downstream gene expression analysis and variant interpretation. Always correlate RNA findings with histopathological assessment and full clinical context. This extraction procedure is a pre‑analytical step and must not be interpreted as a standalone diagnostic result. Our protocol ensures RIN values above 7.0 for optimal sequencing performance."
– Lina Osama Zaki Quteineh | Consultant Medical Genetics | DHA Registration ID: 9294403
Medication Advisory
Do not discontinue or alter any prescribed medication without consulting your treating physician. RNA extraction is a laboratory procedure that does not interact with drug therapy; however, all clinical results must be interpreted in the context of your current treatment regimen.
Exclusion Criteria & Emergency Red Flags
- Patients with active bleeding disorders or uncorrected coagulopathy may develop haematoma at the biopsy or collection site. Alternative sampling methods must be evaluated by the referring physician.
- Extensive tissue necrosis or specimens overfixed in formalin for more than 72 hours may yield degraded RNA unsuitable for downstream molecular analysis. Fresh tissue in RNA stabilizer is required for optimal results.
- Needle phobia or severe anxiety without an accompanying chaperone for biopsy procedures. Patient comfort and safety remain the priority.
- Seek emergency care immediately if: severe pain at the biopsy site, uncontrolled bleeding, swelling, fever, or signs of infection develop within 48 hours of tissue sample procurement.
Patient FAQ & Clinical Guidance
1. How is RNA extracted from solid tumor tissue?
Using silica membrane technology with DNase I treatment, we purify total RNA from biopsy or surgical resection specimens in our ISO 9001:2015 certified laboratory. This method removes genomic DNA contamination and ensures high-purity RNA suitable for sensitive molecular assays including RT-qPCR and NGS. A quality control report with RIN value is provided with every sample to confirm RNA integrity.
2. Does this test require any special preparation before collection?
No fasting or dietary restrictions are required. The procedure requires a fresh tissue sample collected by a healthcare professional in a hospital setting. For surgical specimens, the surgeon places the tissue in an RNA stabilizer solution immediately after resection to preserve nucleic acid integrity. For biopsy samples, our team ensures sterile technique and expedited transport to the laboratory under controlled cold-chain conditions.
3. What happens if my RNA extraction results indicate degradation?
Degraded RNA typically indicates suboptimal sample handling or prolonged warm ischemia time. If the RIN score is below 7.0, the sample may not yield reliable results for downstream applications. In such cases, our clinical team recommends re-collection with immediate stabilization in RNA preservative at 4°C. We provide detailed written guidance for the optimal re-collection protocol and coordinate with your referring physician to minimize diagnostic delay.
4. How are the results delivered and interpreted?
Results are delivered electronically within 5–7 business days via secure digital portal and printed report. A complimentary telephonic consultation with our Consultant Medical Genetics is provided to explain the findings in the context of your clinical history. The report includes RIN value, RNA concentration, purity ratios (A260/280 and A260/230), and a recommendation for appropriate downstream testing.
UAE Regulatory & Data Privacy Adherence
UAE Regulatory Compliance
This service 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. Clinical safety and consent protocols follow Federal Decree-Law No. 4 of 2016 on Medical Liability. All personal health information is encrypted and stored within the UAE. Laboratory licensed by DHA (Facility License: 1143). ISO 9001:2015 certified.
Clinical & Logistical Metadata
| Test Name | RNA Extraction from Solid Tissue |
| Price (AED) | 350 AED |
| Turnaround Time | 5–7 business days |
| Sample Type / Matrix | Hospital Extraction Only – Sample collection is conducted strictly within an accredited hospital facility; mobile home phlebotomy is disabled for safety. |
| Methodology Used | Silica membrane spin columns with DNase I treatment (ISO 9001:2015 certified) |
| ICD-10-CM Code | C80.1 Malignant neoplasm, unspecified |
| LOINC Code | 48018-6 Nucleic acid extraction method |
| DHA Facility License & Laboratory Address | License: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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