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        Time of issue:2021-09-16 17:43:45
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        SARS-CoV-2/Influenza A+B Antigen Combo Rapid Test Kit (Colloidal Gold)
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        The PocRoc? SARS-CoV-2 / Influenza A+B Antigen Combo Rapid Test Kit is used for in vitro qualitative detection of the antigen of novel coronavirus in human throat swabs or nasal swabs. The Flu A/B rapid Test is a colloidal gold enhanced, rapid immunoassay for the qualitative detection of influenza A and influenza B viral nucleoprotein antigens. The test kit is intended for medical professional use only.
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        Product Description
        產品詳細右側內容:

        The PocRoc? SARS-CoV-2 / Influenza A+B Antigen Combo Rapid Test Kit is used for in vitro qualitative detection of the antigen of novel coronavirus in human throat swabs or nasal swabs.

        The Flu A/B rapid Test is a colloidal gold enhanced, rapid immunoassay for the qualitative detection of influenza A and influenza B viral nucleoprotein antigens. The test kit is intended for medical professional use only.

        Intended use

        The PocRoc® SARS-CoV-2 / Influenza A+B Antigen Combo Rapid Test Kit is used for in vitro qualitative detection of the antigen of novel coronavirus in human throat swabs or nasal swabs.

        The Flu A/B rapid Test is a rapid colloidal gold immunoassay for the qualitative detection of influenza A and influenza B viral nucleoprotein antigens. The test kit is intended for medical professional use only.

        Product Information

         

        Production name

        Test samples

        Specifications

        PocRoc® SARS-CoV-2 / Influenza A+B Antigen Combo Rapid Test Kit

        human throat swabs or nasal swabs

        1T/Kit, 5T/Kit, 25T/Kit

        Storage Conditions

        All reagents are ready to use as supplied. Unopened reagent kits are stable at 4°C ~30°C for 24 months tentatively. It should be used within 1 hour once the pouch is opened. Do not freeze the kit or expose the kit above 37°C during storage.

        Samples collection and test procedure

        Sample Collection 

        Nasal Sample CollectionInsert the swab into one nostril of the subject. The swab tip should be inserted up to 2.5 cm (1 inch) from the edge of the nostril. Roll the swab 5 times along the mucosa inside the nostril to ensure that both mucus and cells are collected. Use the same swab; repeat this process for the other nostril to ensure that an adequate sample is collected from both nasal cavities. Withdraw the swab from the nasal cavity.

        Oropharyngeal Sample Collection: The subject sits down, tilts the head back, open the mouth. Make the swab across the tongue to the back wall of the pharynx, tonsil crypts, side walls; Roll the swab 5 times to collect mucosal cells; Gently remove the swab from the mouth to avoid touching the tongue, pituitary gland, oral mucosa and saliva.

        Test preparation

        Do not open the pouch until you are ready to perform a test, and the single-use test is suggested to be used under low environment humidity (RH≤70%) within 1 hour. 

        1. Allow all kit components and samples to reach room temperature between 18°C~26°C before testing.

        2. Remove the test card from the foil pouch and place on a clean dry surface.

        3. Identify the test strip for each sample.

        Test procedure:

        1. Open the package and take out the test strip.

        2. Place the extraction tube on the workbench. The extractor bottle is pressed vertically downward to the extraction tube.

        3. Put the swab sample into the extraction tube, rotate the swab for about 10 seconds, and press the swab head against the tube wall to release the antigen in the swab. Squeeze the swab over the head to remove the swab so as to remove as much liquid as possible from the swab. Dispose of swabs according to biohazard waste disposal method.

        4. Install the beater on the extraction tube, put two drops (around 65μl) into the sample wells separately of the test strip and start the timer.

        5. Read the results in 20 minutes: a strong positive result can be reported within 20 minutes, but a negative result must be reported after 20 minutes, and the result after 30 minutes is no longer valid.

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        Time of issue:2021-06-08 11:15:00

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        Time of issue:2021-09-17 09:20:58

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