| Type: | IVD Reagent |
|---|---|
| Brand: | TianLong |
| Reagents: | HPV PCR Kits |
| Model: | P120H |
| Name: | HPV Nucleic Acid Detection Kit |
| detection of 18 high-risk HPV types: | HPV 16,18,26,31,33,35,39,45,51,52,53, 56,58,59,etc |
| Samples: |
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| Customization: |
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Suppliers with verified business licenses
Audited Supplier Human Papilloma Virus (HPV) Nucleic Acid Detection Kit (Fluorescence PCR Method)
Vaccination rates and the incidence of cervical adenocarcinoma are both on the rise, making HPV genotype testing an important tool to help stratify risk and guide patient management. High-risk HPV genotypes 16, 18 account for 70% of cervical cancer worldwide. Tianlong's Human Papillomavirus (HPV) Nucleic Acid Detection Kit is a qualitative in vitro test for detection of 18 high-risk HPV types (HPV 16,18,26,31,33,35,39,45,51,52,53, 56,58,59,66,68,73 and 82), which can specifically identify types of HPV 16 and HPV 18 while concurrently detecting the rest of other high-risk types.
Intended Use:
The TianLong Human Papilloma Virus(HPV) Nucleic Acid Detection Kit is a qualititative in vitro test for detection of 18 high-risk HPV types(HPV 16,18,26,31,33,35,39,45,51,52,53,56,58,59,66,68,73 and 82) by Real-time Polymerase Chain Reaction (Real-time PCR) method.
This test is designed to detect HPV DNA in specimens such as female cervical epithelial cells.
The potential candidate personnel to be tested could include, but are not limited to patients with symptoms of infection who are suspected of HPV by healthcare providers, or persons with no symptoms from a population for screening test confirmation or exclusion of viral infection or viral carriage status.
Results from the test are for the identification of HPV existence in samples tested. The HPV are mostly often detectable in female cervical epithelial cells samples collected during the acute phase of infection.
High Precision: The coefficient of variation of the Ct values (CV%) is less than 5%
More accurate:Collocating with Tianlong extraction reagent makes your experiment results more accurate
Internal Control: The use of internal control system in the kit can effectively prevent false negative results
User-friendly: Applicable in instruments with FAM ,HEX/VIC,CY5 and TEXAS RED/ROX channels
Concurrently detects remaining 16 HPV genotypes: 26,31,33,35,39,45,51,52,53,56,58,59,66,68,73 ,82 Positive or Negative Pooled Result
| Product Name | Human Papillomavirus (HPV) Nucleic Acid Detection Kit (Fluorescence PCR method) |
| Cat.No | P120H |
| Specification | 32T/kit |
| Sensitivity | 500copies/ml |
| Specimen | Female cervical epithelial cells |
| Type of Analysis | qualitative |
| Storage and Validity | -25ºC~-15ºCfor 12 months |
| Applicable Equipment | Instruments with FAM ,HEX/VIC,Y5 and TEXAS RED/ROX channels, such as ABI7500 real time PCR systems, TL988-IV, Gentier series real time PCR systems |
Suppliers with verified business licenses
Audited Supplier 
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