Newly Arrival China Quantitative Fluorescence Immunoassay Diagnostic Detection Test Kit Wondfo Finecare Progesterone Reagent Test Kit

short description:

Model Number AFP Packing 25 Tests/ kit
Name Diagnostic Kit for Alpha-fetoprotein   Instrument  classification Class II
Features High sensitivity Certificate CE/ ISO13485 
Samples  Blood Shelf life Two Years
Accuracy > 99% Technology Quantitative kit
Storage 2′C-30′C Type Pathological Analysis Equipments


  • Testing time: 10-15 minutes
  • Valid Time: 24 month
  • Accurancy: More than 99%
  • Specification: 1/25 test/box
  • Storage temperature : 2℃-30℃
  • Product Detail

    Product Tags

    Our enhancement depends around the sophisticated devices ,exceptional talents and repeatedly strengthened technology forces for Newly Arrival China Quantitative Fluorescence Immunoassay Diagnostic Detection Test Kit Wondfo Finecare Progesterone Reagent Test Kit, We usually concertrating on acquiring new creative products to fulfill request from our clientele all around the world. Be a part of us and let’s make driving safer and funnier jointly!
    Our enhancement depends around the sophisticated devices ,exceptional talents and repeatedly strengthened technology forces for China Finecare Progesterone, Wondfo Progesterone Test, If you give us a list of merchandise you are interested in, along with makes and models, we can send you quotations. Make sure you email us directly. Our goal is to establish long-term and mutually profitable business relationships with domestic and overseas clients. We look forward to receiving your reply soon.

    Products Parameters

    3AFP

    PRINCIPLE AND PROCEDURE

    PRINCIPLE

    The membrane of the test device is coated with anti AFP antibody on the test region and goat anti rabbit IgG antibody on the control region. Lable pad are coated by fluorescence labeled anti AFP antibody and rabbit IgG in advance. When testing positive sample, the AFP antigen in sample combine with fluorescence labeled anti AFP antibody, and form immune mixture. Under the action of the immunochromatography, the complex flow in the direction of absorbent paper, when complex passed the test region, it combined with anti AFP coating antibody, forms new complex.AFP level is positively correlated with fluorescence signal, and the concentration of AFP in sample can be detected by fluorescence immunoassay assay.

    Test Procedure

    Please read the instrument operation manual and package insert before testing.

    1. Lay aside all reagents and samples to room temperature.
    2. Open the Portable Immune Analyzer(WIZ-A101), enter the account password login according to the operation method of the instrument, and enter the detection interface.
    3. Scan the dentification code to confirm the test item.
    4. Take out the test card from the foil bag.
    5. Insert the test card into the card slot, scan the QR code, and determine the test item.
    6. Add 20μL serum or plasma sample into sample diluent, and mix well..
    7. Add 80μL sample solution to sample well of the card.
    8. Click the “standard test” button, after 15 minutes, the instrument will automatically detect the test card, it can read the results from the display screen of the instrument, and record/print the test results.
    9. Refer to the instruction of Portable Immune Analyzer(WIZ-A101).

    packing

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    About Us

    贝尔森主图_conew1

    Xiamen Baysen Medical Tech limited is a high biological enterprise which devotes itself to filed of fast diagnostic reagent and integrates research and development, production and sales into a whole. There are many advanced research staffs and sales managers in the company, all of them are have rich working experience in china and international biopharmaceutical enterprise.

    Certificate display

    dxgrd


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