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SARS-CoV-2 Antigen Detection Kit Rtk Saliva Accuracy Delta Variant Detection

    Buy cheap SARS-CoV-2 Antigen Detection Kit Rtk Saliva Accuracy Delta Variant Detection from wholesalers
     
    Buy cheap SARS-CoV-2 Antigen Detection Kit Rtk Saliva Accuracy Delta Variant Detection from wholesalers
    • Buy cheap SARS-CoV-2 Antigen Detection Kit Rtk Saliva Accuracy Delta Variant Detection from wholesalers

    SARS-CoV-2 Antigen Detection Kit Rtk Saliva Accuracy Delta Variant Detection

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    Brand Name : KISSH
    Model Number : K903-1
    Certification : CE
    Price : Negotiable
    Payment Terms : T/T
    Supply Ability : 1,000,000 tests per day
    Delivery Time : Within 7 days
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    SARS-CoV-2 Antigen Detection Kit Rtk Saliva Accuracy Delta Variant Detection

    SARS-CoV-2 Antigen Detection Kit(Immunofluorescence)


    Product Information

    Product nameSARS-CoV-2 Antigen Detection Kit(Immunofluorescence)
    Main CompositionTest Cassette individually foil pouched with a desiccant, Sample Tube, with cap and antigen extraction buffer,Sampling swab, Instruction for use
    Package1 Test/Kit
    Keep temperature2-30℃
    Shelf-life12 months
    Place of OriginShenzhen China

    Basis Information

    The SARS-CoV-2 Antigen Detection Kit is a fluorescence immunoassay that is intended for the qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 in nasopharyngeal (NP) and nasal swab, saliva specimens and superficial nasal swab directly from individuals who are suspected of COVID- 19 by their healthcare provider.

    Results are for the identification of SARS-CoV-2 nucleocapsid protein antigen. Antigen is generally detectable in upper respiratory specimens during the acute phase of infection. Positive results indicate the presence of viral antigens, but clinical correlation with patient history and other diagnostic information is necessary to determine infection status. Positive results do not rule out bacterial infection or co-infection with other viruses. The agent detected may not be the definite cause of disease.

    Negative results should be treated as presumptive and confirmed with a molecular assay, if necessary for patient management. Negative results do not rule out COVID- 19 and should not be used as the sole basis for treatment or patient management decisions, including infection control decisions. Negative results should be considered in the context of a patient’s recent exposures, history and the presence of clinical signs and symptoms consistent with COVID- 19.The SARS-CoV-2 Antigen Test is intended for use by trained clinical laboratory personnel and individuals trained in point of care settings.


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