Diagnostic Kit for Heparin Binding Protein

short description:

Diagnostic Kit for Heparin Binding Protein (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

    Diagnostic Kit for Heparin Binding Protein (Fluorescence
    Immunochromatographic Assay)

    Methodology:Fluorescence Immunochromatographic Assay

    Production information

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

     

    INTENDED USE

    This kit is applicable to in vitro detection of heparin binding protein (HBP) in human whole blood/plasma sample,and it 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. This kit only provides heparin binding protein test results, and results obtained shall be used in combination with other clinical information for analysis.

    Test procedure

     1  Before using the reagent,read the package insert carefully and familiarize yourself with the operating procedures.
    2 Select standard test mode of WIZ-A101 portable immune analyzer
    3 Open the aluminum foil bag package of reagent and take out the test device.
    4 Horizontally insert the test device into the slot of immune analyzer.
    5 On home page of operation interface of immune analyzer, click “Standard” to enter test interface.
    6 Click “QC Scan” to scan the QR code on inner side of the kit; input kit related parameters into instrument and select 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.
    7 Check the consistency of “Product Name”, “Batch Number” etc. on test interface with information on the kit label.
    8  Take out sample diluent upon consistent information, add 80μL plasma/whole blood sample, and thoroughly mix them;
    9  Add 80µL aforesaid thoroughly mixed solution into well of test device;
    10 After complete sample addition, click “Timing” and remaining test time will be automatically displayed on the interface.
    11 Immune analyzer will automatically complete test and analysis when test time is reached.
    12 After test by immune analyzer is completed, test result will be displayed on test interface or can be viewedthrough “History” on home page of operation interface.

    Note: each sample shall be pipetted by clean disposable pipette to avoid cross contamination.

    CTNI,MYO,CK-MB-01

    Superiority

    The kit is high accurate,fast and can be transported at room temperature.It's easy to operate.
    Specimen type : Serum/Plasma/Whole Blood

    Testing time:10-15mins

    Storage:2-30℃/36-86℉

    Methodology:Fluorescence Immunochromatographic Assay

     

    Feature:

    •  High sensitive

    •  result reading in 15 minutes

    •  Easy operation

    •  High Accuracy 

     

    CTNI,MYO,CK-MB-04
    HBP Rapid test

     

     

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