Intended Use
To quantitatively detect in vitro nucleic acid amplification assay for the detection of Hepatitis C Virus (HCV) RNA (all genotypes and sub-genotypes) using Real Time PCR System.
Specimen Required
2 Tubes / EDTA Blood / 2 mL per tube or 2 ml Plasma. (Min: 1 mL)
Patient Preparation
- Sample Collection: Collect the blood in lavender (EDTA). Collection of blood before dialysis is preferred.
- Specimen Preparation: Do not freeze. Transport 4 mL whole blood in EDTA tube or 2 mL plasma. (Min: 1 mL)
Storage/Transport - Temperature: Refrigerated
- Unacceptable Conditions: Heparinized specimens
- Remarks: Proper aseptic technique and sample handling are critical to avoid contamination or degradation.
- Stability: Ambient: 24 hrs; Refrigerated: 6 days; Frozen: 6 months
Methodology
This assay uses real time RT-PCR to detect and quantify the target HCV RNA in the patient sample.
Sample Received to Report Turnaround Time (TAT)
Twice in a Week (Scheduled Test)
Reference Interval
Positive or negative for presence of HCV RNA.
Interpretive Data
Refer to the Report.
Resources
- Additional Technical Information
- Test Request Form
Sample Reports
- Enhanced Report
- See report
