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Varicella-Zoster Virus qPCR Kit
Designed for the in vitro detection of HHV3. qPCR assay criteria are met, but PC is not meant for quantification.
Human herpes virus 3 (HHV3), also known as Varicella-zoster virus, is one of the nine known herpes viruses that can infect humans. It causes chickenpox (varicella) commonly affecting children and young adults, and shingles (herpes zoster) in adults but rarely in children. This virus infections are species-specific to humans.
Varicella-Zoster Virus qPCR Kit is designed for the in vitro detection of HHV3 genomes. The kit is built to have the broadest possible detection profile whilst remaining specific to HHV3. Thus, this kit has been designed for the specific (inclusivity) and exclusive (exclusivity) in vitro detection of this species. The primers and probe sequences have very high (>95%) homology with a broad range of HHV3 genomes based on a comprehensive bioinformatic analysis with all reference data within the NCBI database. However, due to the inherent instability of viral genomes, it is not possible to guarantee detection of all clinical isolates. Other closely related virus are not detected. Real-time PCR detection methods have been used in several studies to identify HHV3 genomes (Hong Y.J. et al 2014).
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.
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 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.
Varicella-Zoster Virus qPCR Kit is designed for the in vitro detection of HHV3 genomes. The kit is built to have the broadest possible detection profile whilst remaining specific to HHV3. Thus, this kit has been designed for the specific (inclusivity) and exclusive (exclusivity) in vitro detection of this species. The primers and probe sequences have very high (>95%) homology with a broad range of HHV3 genomes based on a comprehensive bioinformatic analysis with all reference data within the NCBI database. However, due to the inherent instability of viral genomes, it is not possible to guarantee detection of all clinical isolates. Other closely related virus are not detected. Real-time PCR detection methods have been used in several studies to identify HHV3 genomes (Hong Y.J. et al 2014).
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.
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 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 | Human Herpes Virus 3 | Sample Material | DNA | 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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MD05261
- Lyo NZYSupreme qPCR master mix (2x)
- qPCR master mix reconstitution buffer
- Lyo PPMix (10x)
- NTC
- Positive Control
- DNA Internal Extraction Control (IEC)
MD05262
- Lyo PMix 2x
- PMix reconstitution buffer
- NTC
- Positive Control
- DNA Internal Extraction Control (IEC)
- Lyo NZYSupreme qPCR master mix (2x)
- qPCR master mix reconstitution buffer
- Lyo PPMix (10x)
- NTC
- Positive Control
- DNA Internal Extraction Control (IEC)
MD05262
- Lyo PMix 2x
- PMix reconstitution buffer
- NTC
- Positive Control
- DNA 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 | Human Herpes Virus 3 | Sample Material | DNA | 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 | Human Herpes Virus 3 | Sample Material | DNA | 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