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Index > Product > Molecular Diagnostics Platform > Human Papillomavirus(HPV)Genotyping

Human Papillomavirus (HPV) E6/E7 mRNA Genotyping Detection Kit (Fluorescent PCR Melting Curve Method

BIOTRON HPV Panel 14 (BHP14)

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  • This kit is intended for the in vitro qualitative detection of 14  high-risk HPV E6/E7 mRNA genotypes in human cervical exfoliated epithelial cells, including: 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, 68

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  • Regulatory Status:

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DESCRIPTION

Full genotyping results guide cervical cancer risk 

  • stratification and refined management.

For precise cervical cancer screening in women aged 25–64 years, with routine testing recommended every five years for the general population.

Compensates for the limitations of traditional detection methods and enables accurate assessment of cervical lesion risk.


  • Persistent Infection Identification

Sensitively distinguishes between transient HPV infection (which may resolve spontaneously) and persistent infection (with high carcinogenic risk), evaluates HPV activity, and provides early warning of canceration risk.


  • Triage of  high-risk populations

Used for triage of HPV DNA positive people and ASCUS cytology, to more sensitively identify those at risk of progressing to high-grade lesions and avoid unnecessary colposcopy referrals.


  • Follow-up and postoperative monitoring

Effectively identifies the risk of residual or recurrent cervical lesions or cancer following treatment.

SPECIFICATION

  • International Patent

Adopts Multiplex Probe Amplification (MPA) technology,enabling accurate detection of 16+ target genes in a single tube.


  • Single-Tube Full Genotyping detection 

Single-tube sample loading → single-tube reaction → full genotyping results for 14 high-risk HPV E6/E7 mRNA types, focusing on lesion risk and enables precise risk stratification.


  • Excellent Performance

High sensitivity and high specificity, with a lowest detection limit no more than 100 copies/reaction.


  • Convenient Operation

Only 3 steps are needed: nucleic acid extraction → PCR amplification → result analysis,and the entire process can be completed in approximately 2.5 hours..


  • Universal Platform

Compatible with conventional four-channel real-time PCR instruments such as SLAN-96, with low implementation barriers.


  • Higher Throughput

Processes up to 94 samples per single run on one instrument, delivering high efficiency and high throughput.


  • High Biological Safety

Closed-tube amplification and detection throughout the process, eliminating the need to open the tube, effectively preventing aerosol contamination.


  • Software Intelligent Interpretation

Fully automatic data analysis software  for intelligent interpretation of results.


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