Test Price
320 AED✅ Home Collection Available
ASCA Panel IgA & IgG Test in UAE – AED 320 | DHA Licensed Lab
Executive Summary & Core Metrics
Executive Summary – Why Patients Trust Our ASCA Panel
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited processing (Cert: INT/EGQ/2509DA/3139) using quantitative sandwich ELISA methodology for both IgA and IgG isotypes.
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection by DHA-licensed phlebotomists, ISO-certified cold-chain transport (2–8°C), available daily 8 AM to 11 PM.
- Clinical Guidance: Post-test telephonic interpretation with a qualified general practitioner, included in the AED 320 fee.
- Insurance & Support: Direct billing verification and appointment scheduling via WhatsApp +971 54 548 8731. 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.
Test Overview & Methodology
The ASCA Panel measures IgA and IgG antibodies against Saccharomyces cerevisiae, aiding the differential diagnosis of Crohn’s disease versus ulcerative colitis. This ELISA-based profile provides high clinical specificity when correlated with endoscopic and histological findings. The test is performed on serum obtained from a standard SST tube, requiring 2 mL of blood (1 mL minimum).
| Feature | Our ASCA Panel IgA/IgG | Closest Alternative (Single Marker/Non-Panel) |
|---|---|---|
| Methodology | Enzyme-Linked Immunosorbent Assay (ELISA) – Quantitative IgA & IgG | Qualitative or single isotype ELISA |
| Diagnostic Sensitivity / Specificity | ~85% Sensitivity / ~90% Specificity (combined isotypes) | ~70–75% Sensitivity; specificity often lower |
| Turnaround Time | Same-day report if sample received by Thursday 9 AM | 2–3 working days |
| Sample Requirement | 2 mL serum (1 mL min.) from SST; refrigerated or frozen | Often requires separate tubes for IgA and IgG |
| Total Cost (AED) | 320 | 250–350 (may not include consultation) |
Physician Insight & Safety Protocols
Dr. Ajay Singh, General Practitioner (DHA Registration ID: 36234132), shares:
“An elevated ASCA IgA/IgG result provides supportive serological evidence for a Crohn’s disease phenotype, especially when pANCA is negative. However, serology alone cannot replace ileocolonoscopy with biopsy. I advise patients to view this panel as a complementary tool within a complete diagnostic workup. Never adjust therapy based solely on antibody titers without clinical and endoscopic correlation.”
Medication Advisory
Important Medication Warning
Do not discontinue prescribed immunosuppressants, biologics, or any IBD medication without consulting your treating physician. Abrupt cessation may lead to disease flare and serious complications. Always discuss your ASCA results with your doctor before making any treatment changes.
Exclusion Criteria & Emergency Red Flags
- Exclusion: No absolute contraindications. Patients who have received anti-Saccharomyces therapy or anti-fungal prophylaxis within the last 2 weeks should postpone testing to avoid potential interference.
- Red Flags (seek immediate care): Severe cramping abdominal pain, bloody diarrhea exceeding 6 episodes per day, fever above 38.5°C, orthostatic hypotension, or unintentional weight loss greater than 5% in one month – even if ASCA results are pending.
- This test is not for self-diagnosis. A positive result must be interpreted by a qualified physician with full clinical context.
Patient FAQ & Clinical Guidance
1. What is the ASCA IgA and IgG panel used for?
Answer: The ASCA IgA and IgG panel aids in differentiating Crohn’s disease from ulcerative colitis using serological markers, particularly when endoscopic findings are inconclusive. It is not a stand-alone diagnostic tool but a complementary test.
2. How should I prepare for the ASCA panel blood draw?
Answer: No special preparation is required. You can eat and drink normally. Please inform the phlebotomist about any immunosuppressive or biologic therapy you are currently taking.
3. When will I receive my ASCA results and how are they interpreted?
Answer: You will receive your report on the same day if the sample reaches our lab by Thursday 9 AM. A telephonic interpretation by a qualified general practitioner is included in the service fee.
4. Can home collection be arranged for this blood test?
Answer: Yes. Standard peripheral serum collection qualifies for our VIP Mobile Phlebotomy service with temperature-controlled cold-chain transport. A DHA-licensed phlebotomist will visit your home between 8 AM and 11 PM daily.
UAE Regulatory & Data Privacy Adherence
Legal & Privacy Compliance Framework
DNA Labs UAE operates under DHA Facility License Number 1143 and adheres to Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) for all patient data handling. Our clinical testing protocols comply with Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. Patient consent and safety protocols follow Federal Decree-Law No. 4 of 2016 on Medical Liability. Your test results are transmitted through encrypted channels and stored on secure, UAE-based servers.
Clinical & Logistical Metadata
| Test Name | ASCA Panel IgA & IgG |
| Price (AED) | 320 |
| Turnaround Time | Same-day report if sample received by Thursday 9 AM |
| Sample Type / Matrix | Serum (SST, 2 mL, 1 mL minimum) |
| Methodology Used | Quantitative Enzyme-Linked Immunosorbent Assay (ELISA) |
| ICD-10-CM Code | K50.90, K51.90 |
| LOINC Code | 61119-6 (ASCA IgA), 61120-4 (ASCA IgG) |
| DHA Facility License & Laboratory Address | License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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