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Gynaecologic Oncology
Diagnostic Kit for detecting of 16 high-risk and genotyping of 16&18 human papillomavirus (HPV) (PCR fluorescence probe method)

The kit uses real-time multiple fluorescent PCR technology that combined with an automated fully enclosed qPCR instrument. It is used for the in vitro qualitative detection of high-risk HPV16, HPV18 and other 16 high-risk (HPV26, HPV31, HPV33, HPV35, HPV39, HPV45, HPV51, HPV52, HPV53, HPV56, HPV58, HPV68, HPV59, HPV66, HPV73 and HPV82) human papillomavirus (HPV) nucleic acids in cervical exfoliated cells or reproductive tract secretions. The test results can be used for HPV auxiliary diagnosis.

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Advantages

01

Fully enclosed iCassette

02

Preloaded reagent, ready for use

03

Minimal hands-on time

04

Internal control monitors PCR processes

05

No need for freezer storage or transportation

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Comprehensive Multiplex Panels

Product Parameters

Sample Type Cervical exfoliated cells and genital secretions
Turnaround Time Within 2 hours for extraction, amplification, and result analysis
Test Method Magnetic beads extraction, purification, and qPCR method
6-Plexes Detection HPV16, HPV18, HPV26, HPV31, HPV33, HPV35, HPV39, HPV45, HPV51, HPV52, HPV53, HPV56, HPV58, HPV68, HPV59, HPV66, HPV73 and HPV82 and internal control
Sensitivity 1000 copies/ml
Storage Condition 2~28 ℃
Specification 12 reactions/kit 

Application Areas

Clinical diagnostics

Genomics research

Forensic identification