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National Reference Panel Hepatitis E Virus Nucleic Acid Detection Kit Reference Standard
The National Reference Panel provides a set of 15 liquid reference samples for quality control of Hepatitis E virus nucleic‑acid detection kits (PCR‑fluorescent probe, isothermal amplification, etc.). The kit includes negative, positive, precision and detection‑limit specimens prepared from virus‑positive plasma, stool suspensions and other microbial cultures.
Each sample is supplied in a 0.5 mL frozen‑tube and must be stored at –70 °C or lower. Users should fully thaw and mix the specimens before use, perform nucleic‑acid extraction as recommended by the kit manufacturer, and follow the specified dilution and repeat‑testing procedures for performance evaluation. This manual is written in Chinese.
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National Reference Panel Hepatitis E Virus Nucleic Acid Detection Kit Reference Standard
Product Leaflet 3 pages · 137 KB · ZHReference panel for Hepatitis E virus nucleic‑acid detection kits, providing negative, positive, precision and detection‑limit samples.
Questions answered in National Reference Panel manuals
How should the reference samples be stored?
Store the frozen tubes at –70 °C or lower and avoid repeated freeze‑thaw cycles.
From: National Reference Panel Hepatitis E Virus Nucleic Acid Detection Kit Reference Standard
How many negative reference vials are included and what volume does each contain?
Seven negative reference vials (N1‑N7) are provided, each containing 0.5 mL of liquid.
From: National Reference Panel Hepatitis E Virus Nucleic Acid Detection Kit Reference Standard