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SKU
MD07331
Influenza A virus & Influenza B virus RT-qPCR Kit
Influenza A virus & Influenza B virus RT-qPCR Kit is designed for the in vitro detection of Influenza A virus and Influenza B virus genomes. This kit was meticulously designed and validated to meet the rigorous criteria of a quantitative assay. However, it is important to note that the provided Positive Control is not intended for quantification purposes. We recommend checking NZYtech website for the availability of a suitable Quantitative Standard for an accurate quantification. In alternative, commercially genomic DNA standards can also be used.
Availability
Ready to Ship
Influenza A and B viruses are the two primary types responsible for seasonal flu outbreaks in humans, with Influenza A being more genetically diverse and capable of causing pandemics, while Influenza B tends to cause milder illness. Both influenza viruses are highly contagious respiratory diseases transmitted via contact, respiratory droplets (coughing and sneezing) and contaminated surfaces.
Influenza A virus & Influenza B virus RT-qPCR Kit is designed for the in vitro detection of Influenza A and Influenza B viruses. The kit is built to have the broadest possible detection profile whilst remaining specific to Influenza A and Influenza B viruses. Thus, this kit has been designed for the specific (inclusivity) and exclusive (exclusivity) in vitro detection of these viruses. The primers and probe sequences have very high (>95%) homology with a broad range of Influenza A and Influenza B viruses genomes based on a comprehensive bioinformatic analysis with all reference data within the NCBI databases at the time of design. Due to the inherent instability of RNA viral genomes, it is not possible to guarantee the detection of all clinical isolates. This kit was meticulously designed and validated to meet the rigorous criteria of a quantitative assay. However, it is important to note that the provided Positive Control is not intended for quantification purposes. We recommend checking NZYtech website for the availability of a suitable Quantitative Standard for an accurate quantification. In alternative, commercially genomic RNA standards can also be used.
If required, a complementary kit for the detection of an endogenous gene of the species from which samples are being extracted is available for purchase(see Vet, Food & Pharma and Human). The complementary usage of an Endogenous Detection reaction provides a solid confirmation that nucleic acids were properly extracted from the selected biological matrix. If you require further information or have a specific question about the detection profile of this kit, please send an e-mail to info@nzytech.com and our scientific team will answer your question. This kit is designed to be used by trained users in a suitable molecular biology laboratory environment.
Influenza A virus & Influenza B virus RT-qPCR Kit is designed for the in vitro detection of Influenza A and Influenza B viruses. The kit is built to have the broadest possible detection profile whilst remaining specific to Influenza A and Influenza B viruses. Thus, this kit has been designed for the specific (inclusivity) and exclusive (exclusivity) in vitro detection of these viruses. The primers and probe sequences have very high (>95%) homology with a broad range of Influenza A and Influenza B viruses genomes based on a comprehensive bioinformatic analysis with all reference data within the NCBI databases at the time of design. Due to the inherent instability of RNA viral genomes, it is not possible to guarantee the detection of all clinical isolates. This kit was meticulously designed and validated to meet the rigorous criteria of a quantitative assay. However, it is important to note that the provided Positive Control is not intended for quantification purposes. We recommend checking NZYtech website for the availability of a suitable Quantitative Standard for an accurate quantification. In alternative, commercially genomic RNA standards can also be used.
If required, a complementary kit for the detection of an endogenous gene of the species from which samples are being extracted is available for purchase(see Vet, Food & Pharma and Human). The complementary usage of an Endogenous Detection reaction provides a solid confirmation that nucleic acids were properly extracted from the selected biological matrix. If you require further information or have a specific question about the detection profile of this kit, please send an e-mail to info@nzytech.com and our scientific team will answer your question. This kit is designed to be used by trained users in a suitable molecular biology laboratory environment.
Shipping Conditions | Room Temperature |
---|---|
Storage Conditions | -85°C to -15°C |
Format | Lyophilized |
Product Category | Predesigned qPCR assays |
Compatibility | All standard Real-time thermal cyclers |
Target Species | Influenza A virus & Influenza B |
Sample Material | RNA |
Protocol time | Approx. 60 min (from extracted NA to result) |
Number of targets | Triplex |
Internal Control | No |
Features | Free automatic data analyzer (Fastfinder) |
Detection Method | Probe Based |
- Lyo NZYSupreme One-step RT-qPCR Master Mix (2x)
- RT-qPCR master mix reconstitution buffer
- Lyo PPMix (10x)
- NTC
- Positive Control
- RNA Internal Extraction Control (IEC)
- RT-qPCR master mix reconstitution buffer
- Lyo PPMix (10x)
- NTC
- Positive Control
- RNA Internal Extraction Control (IEC)
Shipping Conditions | Room Temperature |
---|---|
Storage Conditions | -85°C to -15°C |
Format | Lyophilized |
Product Category | Predesigned qPCR assays |
Compatibility | All standard Real-time thermal cyclers |
Target Species | Influenza A virus & Influenza B |
Sample Material | RNA |
Protocol time | Approx. 60 min (from extracted NA to result) |
Number of targets | Triplex |
Internal Control | No |
Features | Free automatic data analyzer (Fastfinder) |
Detection Method | Probe Based |
Shipping Conditions | Room Temperature |
---|---|
Storage Conditions | -85°C to -15°C |
Format | Lyophilized |
Product Category | Predesigned qPCR assays |
Compatibility | All standard Real-time thermal cyclers |
Target Species | Influenza A virus & Influenza B |
Sample Material | RNA |
Protocol time | Approx. 60 min (from extracted NA to result) |
Number of targets | Triplex |
Internal Control | No |
Features | Free automatic data analyzer (Fastfinder) |
Detection Method | Probe Based |
MSDS
Material Safety Data Sheets
CoA
Certificate of Analysis