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Reagent

Human Papillomavirus Assay

Ongoing Challanges

  • The WHO estimates the global burden of cervical cancer will rise to 700,000 cases and 400,000 deaths by 2030. Over 95% of cervical cancers are due to HPV infection.

  • The high-risk genotypes HPV 16 and 18 cause approximately 70% of cervical cancers. HPV 6 and 11 cause the majority of anogenital warts.

  • The WHO strongly recommends HPV DNA detection as the primary screening test over VIA or cytology.

REFERENCE
1. WHO Europe (2021). Newsletter: WHO recommends DNA testing as a first-choice screening method for cervical cancer prevention.
2. WHO. Cervical cancer

Product Overview

The EasyNAT® Human Papillomavirus Assay is a fast and sensitive DNA test to aid in the diagnosis of sexually transmitted HPV infections, specifically detecting types 6, 11, 16, and 18.

  • Results available within 51 minutes

  • Designed to provide an accurate LOD: 1000 copies/mL

  • Aids in the early diagnosis of HPV to help prevent potential HPV-attributable cancers.

Clinical Value

  • A fast and sensitive DNA test to aid in diagnosing sexually transmitted HPV infections.

  • Detects and distinguishes between HPV types 6, 11, 16, and 18.

  • Offers early identification of HPV infection, helping to prevent potential HPV-attributable cancers.

Product Resources

EasyNAT® Human Papillomavirus Assay
Brochure
EasyNAT® Human Papillomavirus Assay
Instructions for Use
EasyNAT® Human Papillomavirus Assay
SOP
Reagent
System

MultNAT

PortNAT

EasyNAT

Solution
Primary
Healthcare
Sexually Trasmitted Infections
Public Health
Tuberculosis
Respiratory
Infections
Livestock
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