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Novel Coronavirus 2019-nCoV Rapid Detection Kit (LAMP)
  • Introduction

    Certifications: CE certification, Philippines, and Thailand FDA cert🅠ifica🅠tion, Import License of UAE

     

     

  • Usage

    This kit is used for in vitro qualitative and rapid detection of (2019-nCoV) ORF1ab gene in human nasopharyngeal swab sampl༒es.

  • Product Information

    Packaging Size: 96 tests/kit

  • Sample Requirements

    Storage Conditions: The collected samples shall be submitted for ꦿdetection in 🌼time.

    Validity Period: 2-8ºC, 24 hours; 
    Below -70ºC: 6 months, avoid repeated freezing and thawing. 
    Requirements of Sample Processing:
    1. Nasopharyngeal swab: nucleic acid extraction or inactivation treatment.
    2. Throat swab: nucleic acid extraction.

  • Storage Conditions and Validity Period

    Storage Conditions: -20±5°C
    Validity Period: stated on the label of each product🍬.

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