Bovine herpesvirus 1 qPCR Kit
Catalogue Number: MD05161-NZY
| Manufacturer: | NZYTech |
| Type: | qPCR Kits |
| Shipping Condition: | RT |
| Storage Condition: | -70°C |
| Unit(s): | 100 reactions |
| Application: | qPCR |
Description
Description: Bovine herpesvirus 1 (BHV-1) is a virus of the family Herpesviridae known to cause several diseases worldwide in cattle, including rhinotracheitis, vaginitis, balanoposthitis, abortion, conjunctivitis, and enteritis. It is spread horizontally through sexual contact, artificial insemination, and aerosol transmission and it may also be transmitted vertically across the placenta. Bovine herpesvirus 1 qPCR Kit is designed for the in vitro detection of BHV-1 genomes. The kit is built to have the broadest possible detection profile whilst remaining specific to BHV-1. 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 BHV-1 genomes based on a comprehensive bioinformatic analysis with all reference data within the NCBI database. Other closely related species are not detected. Real-time PCR detection methods have been used in several studies to identify BHV-1 genomes (Wang J. et al 2007). 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 Vet, Food & Pharma). 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.
Additional Text
Short Description
Bovine herpesvirus 1 qPCR Kit is designed for the in vitro detection of BHV-1 genomes.
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