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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Product Detail

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Advantages

● Fully enclosed iCassette

● Preloaded reagent, ready for use

● Minimal hands-on time

● Internal control monitors PCR processes

● No need for freezer storage or transportation

● Comprehensive multiplex panels

Parameters

Sample Type	Cervical exfoliated cells and genital secretions
Turnaround Time	With in 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	1000copies/mL
Storage Condition	2~28 ℃
Specification	12 reactions/kit