Reagent Kit for Detection and Differentiation of Human Papillomavirus (HPV) DNA Genotypes 16 and 18 Using PCR with Hybridization-Fluorescent Detection "AmpliSens® HPV 16/18-FL" (TU 9398-063-01897593-2012) Reagent Kit for Detection and Differentiation of Human Papillomavirus (HPV) DNA Genotypes 16 and 18 Using PCR with Hybridization-Fluorescent Detection "AmpliSens® HPV 16/18-FL" (TU 9398-063-01897593-2012) The "AmpliSens® HPV 16/18-FL" reagent kit is designed for the detection and differentiation of Human Papillomavirus (HPV) DNA genotypes 16 and 18 in clinical samples using polymerase chain reaction (PCR) with hybridization-fluorescent detection. Manufactured in accordance with TU 9398-063-01897593-2012. Available Formats: Format FEP: Form 1: PCR Kit variant FEP-100 F Form 2: PCR Kit variant FEP (0.5 ml tubes) Form 3: PCR Kit variant FEP (0.2 ml tubes) Form 4: DNA-sorb-AM kit (variant 100) + PCR Kit variant FEP-100 F Form 5: DNA-sorb-AM kit (variant 100) + PCR Kit variant FEP (0.5 ml tubes) Form 6: DNA-sorb-AM kit (variant 100) + PCR Kit variant FEP (0.2 ml tubes) Format FRT: Form 1: PCR Kit variant FRT-100 F Form 2: PCR Kit variant FRT Form 3: DNA-sorb-AM kit (variant 100) + PCR Kit variant FRT-100 F Form 4: DNA-sorb-AM kit (variant 100) + PCR Kit variant FRT If your organization wants to sell medical equipment, medical products or medical consumables in Russia, for example, Reagent Kit for Detection and Differentiation of Human Papillomavirus (HPV) DNA Genotypes 16 and 18 Using PCR with Hybridization-Fluorescent Detection "AmpliSens® HPV 16/18-FL" (TU 9398-063-01897593-2012), 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. Старая цена: 0.00 EUR Back Copyright MAXXmarketing GmbHJoomShopping Download & Support