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Address: No. 189 Taihang Avenue, High-tech Zone, Shijiazhuang City, Hebei Province

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Porcine Pseudorabies Virus Fluorescent PCR Detection Kit

  • Commodity name: Porcine Pseudorabies Virus Fluorescent PCR Detection Kit
  • Commodity ID: 1468554201741807616
  • Product Description
  • [ Intended Use 】

    This kit is suitable for detecting porcine pseudorabies virus in tissues or blood samples.

    [ Detection Principle 】

    This reagent uses a pair of specific primers for porcine pseudorabies virus, combined with a fluorescent probe, and employs fluorescence quantitative PCR technology to amplify the DNA of porcine pseudorabies virus in vitro, enabling pathogen diagnosis of suspected samples in clinical settings.

    [ Packaging specifications 50T/box

    [ Reagent composition 】

    [ Reagent Storage Conditions and Shelf Life 】

    -20℃ to +5℃; store and transport away from light; avoid repeated freeze-thaw cycles for more than 8 times. Shelf life: 12 months.

    [ Sample Preservation and Transportation 】

    The above-mentioned samples can be stored at -20℃ for short-term preservation and at -70℃ for long-term storage, but the storage duration should not exceed 6 months. Samples must be transported using ice packs maintained at 2-8℃, and repeated freeze-thaw cycles are strictly prohibited.

    [ Instructions for use 】

    1. Sample processing: DNA extraction

    It is recommended to use the viral nucleic acid co-extraction kit from Shijiazhuang Shengbo Biotechnology Co., Ltd. for DNA extraction from samples. Please follow the instructions provided in the reagent manual.

    2. Add sample

    After the qRT-PCR reaction mixture has naturally thawed, pipette 17 μl into a PCR tube. Then, add 3 μl each of the DNA extracted in Step 1, as well as the positive control and negative control, respectively, into the qPCR reaction tubes. Close the tubes tightly, mix thoroughly, and briefly centrifuge.

    3. PCR amplification

    3.1 Place the reaction tube into the fluorescence quantitative PCR reaction chamber.

    3.2 Set the sample name and channel information.

     

    To determine how to interpret the test results, please contact our company!

Qualification Compliance Advantage:

On October 12, 2019, we successfully passed the GMP inspection for veterinary biological diagnostic products, ensuring that our production qualifications meet the industry’s high standards and that we possess the necessary conditions for legitimate production and operation.

Hardware standard advantages:

A biopharmaceutical workshop of over 400 square meters has been established, strictly adhering to GMP standards. It is equipped with high-specification, standardized production lines, ensuring highly standardized and professional production hardware.

Industrial scale advantage:

The company covers an area of over 50 mu and boasts a large-scale production facility that ensures stable production operations and full capacity utilization.

Full-industry-chain advantages:

Establish an integrated operational model for the R&D, production, sales, and technical services of veterinary biological products, with a comprehensive business layout and strong capabilities to align integrated services with market demands.

Location-based development advantages:

Located in the Shijiazhuang High-Tech Industrial Development Zone, it can leverage the zone’s industrial support systems and policy advantages to help enterprises advance their research and business development.

Enterprise Positioning Advantages:

Positioned as a comprehensive, modern, high-tech enterprise, we focus on the field of veterinary biological products and possess characteristics of technological advancement and modernization, aligning with industry development trends.

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