High-risk HPV 16+2

High-risk Human Papillomavirus Nucleic acids Detection Kit (PCR-fluorescence probe method) 16+2 Typing.

Detection index: Simultaneous detection of 18 HPV high-risk types in the same reaction tube.

Specific types: 16, 18.

Sixteen (16) common high-risk types: 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, 68, 82, 26, 53, 73

Intended use: Detection of 18 Human papillomavirus genotypes in cervical exfoliated cell samples and genitourinary secretions.

Registration No.:  20163400763, CE marked.

Packing specifications: single tube, 24 tests/box.

Storage conditions and expiration date: Store at -20±5°C, avoid repeated freezing and thawing; the validity period is nine (9) months from the production date indicated on the box.

Transportation: Use dry ice (or blue ice) to keep cool. The detection performance of this kit is not affected within 72 hours. The detection performance is not affected within 8 hours after opening (thawing).

Product advantages:

- Large detection spectra: Eighteen 18 common high-risk subtypes are simultaneously tested in the same reaction tube, and 16 and 18 types are specifically classified.

- Direct rapid PCR reaction: A new generation of FAST-Taq DNA polymerase with hot start, rapid amplification and anti-inhibitory properties can amplify the sample to ensure sensitivity and specificity; dUTP+UDG enzyme anti-pollution system is added to the amplification system to avoid contamination. Internal standard quality control, monitoring sample extraction, amplification, to avoid false positives.

- Full color-tracking system: The extracted sample solution contains a blue tracer, which can indicate whether the template is added or not, and reduces the sampling error.

- General equipment: PCR instrument with four (4) fluorescent channels (FAM, TXERD, HEX, CY5) or above, such as ABI7500, AGS4800, etc.

- Simple and fast: Single-tube single-serving packaging, without reagent preparation, the whole experimental process is less than 1.5 hours.