【Product Name】

Detection Kit for Human Papilloma Virus 16/18 DNA (PCR-Fluorescence Probing)

【Intended Use】 

This kit is used to qualitatively detect the nucleic acid of Human Papilloma Virus 16/18 in male urethral swab samples, female cervical swab samples in vitro. The test results can be used for auxiliary diagnosis of sexual transmission and  reproductive tract infectious diseases caused by human papilloma virus type 16 and type 18. The test results are only for clinical reference and should not be  used as the sole criterion for clinical diagnosis.

【Principle】  

This kit uses real-time fluorescence PCR detection technology to achieve  qualitative detection of HPV type 16 and type 18 in genitourinary tract secretion  samples by using a pair of specific primers and a specific fluorescent probe in  the conserved region shared by human papillomavirus (HPV) type 16 and type  18. 

This kit sets internal control, to monitor the presence of PCR inhibitors in the  samples by detecting whether the internal control is normal, so as to avoid PCR  false negative result.

【Sample Requirements】  

Applicable sample types: male urethral swab samples, female cervical swab  samples.

【Material Required but Not Provided】  

Amplification Instrument: ABI7500, ABI 7500 Fast and other Real-time  fluorescence PCR instrument with FAM and VIC channels. 

Vortex shaker, centrifuge, pipette sets with tips (10μL, 20μL, 1000μL), PCR tubes,  clean bench and Bio Safety Cabinet (BSC), disposable gloves, shoe covers, hats,  eyes shields and personal protective equipment (PPE).

【Storage Conditions and Term of Validity】

Store below 30°C. It is valid for 12 months.