Reagent Kit for Qualitative, Quantitative Detection and Differentiation of High-Risk Human Papillomavirus (HPV) DNA Genotypes 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, 68 by PCR
The reagent kit is designed for the qualitative and quantitative detection and differentiation of high-risk human papillomavirus (HPV) DNA genotypes 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, and 68 in biological samples using polymerase chain reaction (PCR).
This product complies with TU 9398-226-01897593-2016 and is marketed under the name “AmpliSens® HPV HR genotype-titer-FL”.
Kit Configuration
PCR Kit, FRT-100 FN Variant includes:
- PCR Mix-FL HPV 1 – 1 tube
- PCR Mix-FL HPV 2 – 1 tube
- PCR Mix-FL HPV 3 – 1 tube
- PCR Mix-FL HPV 4 – 1 tube
- PCR Buffer-N – 4 tubes
- K1 HPV Genotype Control – 4 tubes
- K2 HPV Genotype Control – 4 tubes
The kit also includes the “AmpliSens® HPV HR genotype-titer” software version 1.0 for data analysis.
If your organization wants to sell medical equipment, medical products or medical consumables in Russia, for example, Reagent Kit for Qualitative, Quantitative Detection and Differentiation of High-Risk Human Papillomavirus (HPV) DNA Genotypes 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, 68 by PCR, then our information portal MEDCOMMERCE can help you with this. To do this, simply fill out the feedback form by clicking on the link FEEDBACK FORM.
The products posted on our website are approved for use in Russia by the state regulator Roszdravnadzor (Federal Service for Surveillance in Healthcare). The information is for informational purposes only.
