AmpFire HPV Screening 16/18/HR
The AmpFire HPV Screening 16/18/HR kit is an in vitro nucleic acid isothermal amplification with real time fluorescence detection assay for the qualitative detection of DNA from Human Papillomavirus (HPV) genotypes 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, 68 and simultaneously identify HPV16 and HPV18, the two most dangerous HPV genotypes, from different sample types.
Each kit includes 100 tests.
This product is CE-IVD certified. It is for research use only in US.
AmpFire HPV Screening 16/18/HR
The AmpFire HPV Screening 16/18/HR is an isothermal nucleic acid amplification assay for the qualitative detection of high-risk types of human papillomavirus (HPV). High risk HPV specific primers and fluorescent probes are used to amplify regions of viral genomic DNA including E6/E7 regions under isothermal conditions. The assay detects HPV types 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, and 68 and allows simultaneous identification of the HPV 16 & 18.
Human papillomavirus (HPV) is the most common sexually transmitted virus in the world. In most cases, HPV infections are transient, and the body will clear the virus on its own. In some instances, however, the virus is persistent and will cause normal cells to become abnormal, leading to cancer.
These oncogenic types of HPV are classified as high risk and include HPV 16 and 18. Other types are considered low risk, as they do not appear to cause cancer.
According to the World Health Organization (WHO), HPV is the second biggest cause of female cancer mortality worldwide, claiming about 250,000 lives annually. In Europe alone, the disease claims about 15,000 lives each year. It is estimated that nearly 70% of cervical cancers are caused by HPV types 16 and 18.
Features Include
Technical Specs
Workflow Overview for the AmpFire HPV Screening 16/18/HR
This section is for demonstrative purposes only and may be incomplete or inaccurate. Always refer to the product instructions for precise guidelines and directions.