| Product Name | Hepatitis B Virus Nucleic Acid Test Kit (Fluorescent PCR Method) |
| Catalog No. | BDDK-HMM-0001 |
| Description | This product is mainly designed for hepatitis B patients receiving antiviral therapy, and is used to assess the response to antiviral therapy and monitor treatment efficacy by monitoring the baseline level and changes of HBV DNA in the blood of patients with hepatitis B. The product is mainly designed for hepatitis B patients receiving antiviral therapy. |
| Disease Type | Hemovirus Disease |
| Applications | This kit is for the in vitro quantitative detection of Hepatitis B virus (HBV) DNA in human serum/plasma samples. |
| Sample Type | Serum or plasma |
| Detection Methods | Fluorescent PCR Method |
| Sensitivity | Minimum detection limit 5 IU/mL |
| Detection Range | 10-1.0×10^9 IU/mL |
| Accuracy | Absolute deviation of quantitative values < 0.5; coefficient of variation < 5% |
| Storage | Store at -20°C away from light. |
| Shelf Life | 9 months |
| Features | The exogenous internal standard can realize the whole process of monitoring the extraction of DNA from the sample to be tested and the amplification efficiency of the PCR reaction, which can avoid false negatives due to the presence of inhibitors in the sample or operational errors; the UDG enzyme anti-pollution measures are adopted to prevent false positives that may be caused by product contamination. |
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