Diagnostic Kit for Human Papilloma Virus 14 High-Risk Genotyping DNA (Real-Time PCR Method)
2025-02-17Hepatitis C Virus Nucleic Acid Detection Kit (Real-Time PCR Method)
2025-02-19Detection Kit for Human Papilloma Virus 16/18 DNA
Product Number: QDHPV16/18
Shipping and Storage
- Store below 30°C. It is valid for 12 months.
- Date of manufacture and term of validity: see the label.
- Transport at normal temperature, not suggested over 14 days.
- Opened but not completely used HPV 16/18 PCR Master Mix should be stored at (-20±5) °C. It is recommended to separate in PCR tubes before refrigeration to avoid repeated freezing and thawing of all reagents next time. Storage time should not exceed 21 days.
Components
| Reagent | QDHPV16/18 48T | Ingredients |
| HPV 16/18 PCR Master Mix | Lyophilized powder | Contains target gene primers, probes, reaction buffer, dNTPs, Mg2+, Taq Enzyme |
| Redissolved Diluent | 1.40ml | Purified water |
| HPV 16/18 Positive Control | Lyophilized powder | Recombinant plasmid containing target gene |
| HPV 16/18 Negative Contro | 0.25ml | Physiological saline |
Note：Do not mix reagents from different batches.
Description
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.
Application
This kit is used to qualitatively detect the nucleic acid of Human Papilloma Virus16/18 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 16and type 18. The test results are only for clinical reference and should not be used as the sole criterion for clinical diagnosis.
