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T-cell surface glycoprotein CD5, Cd5 ELISA KIT/ Mouse T-cell surface glycoprotein CD5, Cd5 ELISA试剂盒

产品信息
  • Mouse Cluster of differentiation 5, CD5 ELISA Kit
    96 Tests
    Operating instruction

    FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS!PLEASE READ THROUGH ENTIRE PROCEDURE BEFORE
    BEGINNING!

    Synonyms
    T-cell surface glycoprotein CD5,Lymphocyte antigen T1/Leu-1, CD5,CD5 molecule; T-cell surface glycoprotein CD5; CD5 antigen
    (p56-62); LEU1; lymphocyte antigen T1/Leu-1

    Search name
    Mouse Cluster of differentiation 5 ELISA Kit, Mouse CD5 ELISA Kit, Mouse T-cell surface glycoprotein CD5 ELISA Kit, Mouse
    Lymphocyte antigen T1/Leu-1 ELISA Kit, Mouse Lymphocyte antigen T1ELISA Kit, Mouse Leu-1 ELISA Kit, Mouse CD5
    molecule ELISA Kit, Mouse CD5 antigen ELISA Kit, Mouse p56-62 ELISA Kit, Mouse LEU1 ELISA Kit

    Intended use
    This immunoassay kit allows for the in vitro quantitative determination of mouse t-cell surface glycoprotein cd5,T-cell surface glycoprotein
    CD5 concentrations in serum, Plasma, tissue homogenates and Cell culture supernates and Other biological fluids.

    Test principle
    The microtiter plate provided in this kit has been pre-coated with an antibody specific to T-cell surface glycoprotein CD5. Standards or
    samples are then added to the appropriate microtiter plate wells with a biotin-conjugated polyclonal antibody preparation specific for T-cell
    surface glycoprotein CD5 and Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then
    a TMB substrate solution is added to each well. Only those wells that contain T-cell surface glycoprotein CD5, biotin-conjugated antibody
    and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of a sulphuric
    acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of T-cell
    surface glycoprotein CD5 in the samples is then determined by comparing the O.D. of the samples to the standard curve.

     


     

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