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Hepatitis C virus RT-qPCR Kit
Designed for the in vitro detection of HCV. qPCR assay criteria are met, but PC is not meant for quantification.
Hepatitis C virus (HCV) is a bloodborne pathogen responsible for causing hepatitis C, a liver infection that can range in severity from a mild illness lasting a few weeks to a chronic, lifelong condition. HCV belongs to the Flaviviridae family and is a single-stranded RNA virus. The most common modes of transmission include exposure to infected blood or bodily fluids, and less commonly, through sexual contact or from an infected mother to her baby during childbirth. Hepatitis C virus RT-qPCR Kit is designed for the in vitro detection of Hepatitis C virus.
The kit is built to have the broadest possible detection profile whilst remaining specific to HCV. Thus, this kit has been designed for the specific (inclusivity) and exclusive (exclusivity) in vitro detection of this virus. The primers and probe sequences have very high (>95%) homology with a broad range of HCV 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 at NZYtech (see https://nzytech.com/en/molecular-diagnostics/). 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.
The kit is built to have the broadest possible detection profile whilst remaining specific to HCV. Thus, this kit has been designed for the specific (inclusivity) and exclusive (exclusivity) in vitro detection of this virus. The primers and probe sequences have very high (>95%) homology with a broad range of HCV 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 at NZYtech (see https://nzytech.com/en/molecular-diagnostics/). 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 | Hepatitis C virus | Sample Material | RNA | Protocol time | Approx. 60 min (from extracted NA to result) | Number of targets | Duplex | Internal Control | No | Detection Method | Probe Based |
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MD07671
- 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)
MD07672
- Lyo PMix 2x
- PMix reconstitution buffer
- NTC
- Positive Control
- RNA Internal Extraction Control (IEC)
- 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)
MD07672
- Lyo PMix 2x
- PMix reconstitution buffer
- 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 | Hepatitis C virus | Sample Material | RNA | Protocol time | Approx. 60 min (from extracted NA to result) | Number of targets | Duplex | Internal Control | No | Detection Method | Probe Based |
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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 | Hepatitis C virus | Sample Material | RNA | Protocol time | Approx. 60 min (from extracted NA to result) | Number of targets | Duplex | Internal Control | No | Detection Method | Probe Based |
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MSDS
Material Safety Data Sheets
CoA
Certificate of Analysis