Influenza A (H1N1) TaqMan RT-PCR Detection Kit Dx (Cat. DxTM27900)
Influenza A (H1N1) TaqMan RT-PCR Detection Kit Dx
![H1N1 Detection Kit (24 reactions)](https://norgenbiotek.com/sites/default/files/styles/original/public/images/product_images/TM27900-Taqman-24rxn-WEB_0.jpg?itok=4OwMznqI" "H1N1 Detection Kit (24 reactions)")
- Professional Tech Support with Senior R&D Scientist
- Fast and Flexible Ordering Options (online, email, or phone)
- Volume Discounts Available on Large Quantity Orders*
*Inquire by phone or email for more information.
Influenza A (H1N1) TaqMan RT-PCR Detection Kit Dx
- Detection kits for H1N1
- CE-IVDD marked in accordance with the European Commission Directive 98/79/EC.
- Research version available
- Available in TaqMan format for analysis
Intended for in vitro diagnostics use.
CE marked version is not available for sale in the United States and Canada
Want a discount?
Create your account to receive 15% off on your first purchase!
(Cat. DxTM27900) 24 rxn
Product Format Norgen Biotek offers kits in different standardized formats. You can view and compare kit components in the Components Table in the Product Overview section. For more information on format types, please visit our Format Information page.
Product Size
Kit Specifications
Storage Conditions
The H1N1 TaqMan RT-PCR Kit Dx is shipped on dry ice. The components of the kit should be frozen upon arrival. If one or more of the components is not frozen when the kit is received, or if any of the components have been compromised during shipment, please contact Norgen Biotek for assistance. All kit components should be stored at -20°C upon arrival. Repeated thawing and freezing (> 3 x) of the Master Mix and Positive Control should be avoided, as this may affect the performance of the assay. If the reagents are to be used only intermittently, they should be frozen in aliquots.
Supporting Data
Influenza A (H1N1) TaqMan RT-PCR Detection Kit Dx
Influenza is caused by three immunologic types of RNA viruses (A, B and C) within the Orthomyxoviridae family. Seasonal influenza is typically caused by three major subtypes of hemaglutinin (H1, H2 and H3) and two subtypes of neuraminidase (N1 and N2). A novel sub-type of influenza A virus called pandemic H1N1 2009 virus was identified in Mexico and reported by the CDC and WHO in April, 2009 (Novel swine-origin influenza A (H1N1) virus investigation team, 2009; CDC, 2009; and Fraser et al., 2009). H1N1 2009 is a novel sub-type virus that transmits easily between humans with 21 countries reporting cases within a month of initial identification (CDC, 2009-b). It is essential that public health laboratories around the world undertake detailed surveillance to monitor the spread and impact of pandemic H1N1 2009 virus as well as try to predict future changes in virulence (Fraser et al., 2009). Methods for the rapid diagnosis, case identification and tracking of this novel pathogen in the human population are therefore required to develop appropriate management strategies to mitigate morbidity and mortality.
Click to expand options
- Ready to use format, including Master Mix for the target and PCR control to monitor for PCR inhibition and validate the quality
- Specific Primer and Probe mix for the pathogen/virus/viroid of interest
- Primer and Probe mix
- Positive and negative control to confirm the integrity of the kit reagents
Supporting Data
Kit Specifications
Storage Conditions
The H1N1 TaqMan RT-PCR Kit Dx is shipped on dry ice. The components of the kit should be frozen upon arrival. If one or more of the components is not frozen when the kit is received, or if any of the components have been compromised during shipment, please contact Norgen Biotek for assistance. All kit components should be stored at -20°C upon arrival. Repeated thawing and freezing (> 3 x) of the Master Mix and Positive Control should be avoided, as this may affect the performance of the assay. If the reagents are to be used only intermittently, they should be frozen in aliquots.
