Diagnostic Kit for Free Thyroxine

short description:

 Diagnostic Kit for  Free Thyroxine 

Methodology: Fluorescence Immunochromatographic Assay

 


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

    Product Tags

    Production information

    Model Number FT4 Packing 25 Tests/ kit, 30kits/CTN
    Name Diagnostic Kit for Free Thyroxine Instrument  classification Class II
    Features High sensitivity, Easy opeation Certificate CE/ ISO13485
    Accuracy > 99% Shelf life Two Years
    Methodology Fluorescence Immunochromatographic Assay
    OEM/ODM service Avaliable

     

    FT4-1

    Summary

    Heparine-binding protein is a protein molecule released by azurophilic granule of activated neutrophil. As an
    important granulin secreted by neutrophil, it can activate monocyte and macrophage, and has significant
    antibacterial activity, chemotactic features and the effect of regulation of inflammatory response. Laboratory
    studies indicate the protein can also modify endothelial cells, cause blood vessel leakage, facilitate migration of
    white blood cells toward infection site, and increase Vaso permeability. According to research report, HBP can be
    used for auxiliary disease diagnosis, such as respiratory and circulatory failure, severe sepsis, urinary tract
    infection in children, bacterial skin infection and acute bacterial meningitis.

     

    Feature:

    •  High sensitive

    •  result reading in 15 minutes

    •  Easy operation

    • Factory direct price

    •  need  machine for result reading

    FT4-3

    Intended Use

    This kit is applicable to in vitro quantitative detection of free thyroxine (FT4) in human serum/plasma/whole blood sample, which’s mainly used for assessment of thyroid function. This kit only provides free thyroxine (FT4) test results, and results obtained shall be used in combination with other clinical information for analysis. It must only be used by healthcare professionals.

    Test procedure

     1 I-1: Use of portable immune analyzer
     2  Open the aluminum foil bag package of reagent and take out the test device.
     3 Horizontally insert the test device into the slot of immune analyzer.
     4 On home page of operation interface of immune analyzer, click “Standard” to enter test interface.
     5 Click “QC Scan” to scan the QR code on inner side of the kit; input kit related parameters into instrument andselect sample type.Note: Each batch number of the kit shall be scanned for one time. If the batch number has been scanned, then
    skip this step.
     6  Check the consistency of “Product Name”, “Batch Number” etc. on test interface with information on the kit label.
     7  Start to add sample in case of consistent information:Step 1: slowly pipette 80μL serum/plasma/whole blood sample at once, and pay attention not to pipette bubbles;
    Step 2: pipette sample to sample diluent, and thoroughly mix sample with sample diluent;
    Step 3: pipette 80µL thoroughly mixed solution into well of test device, and pay attention no to pipette bubbles
    during sampling
     8  After complete sample addition, click “Timing” and remaining test time will be automatically displayed on theinterface.
     9  Immune analyzer will automatically complete test and analysis when test time is reached.
    10  After test by immune analyzer is completed, test result will be displayed on test interface or can be viewed through“History” on home page of operation interface.

    Factory

    Exhibition

    exhibition1

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