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Tick-Borne Encephalitis Virus IgG and IgG Avidity Kit ELISA

Ce kit ELISA Humain est un kit ELISA Colorimetric conçu pour quantifier Humain .
N° du produit ABIN459372

Aperçu rapide pour Tick-Borne Encephalitis Virus IgG and IgG Avidity Kit ELISA (ABIN459372)

Antigène

Tick-Borne Encephalitis Virus IgG and IgG Avidity

Reactivité

Humain

Méthode de détection

Colorimetric

Type de méthode

Indirect ELISA

Application

ELISA

Type d'échantillon

Serum, Plasma
  • Fonction

    anti-TBEV IgG and IgG avidity is a solid-phase immunoanalytical test.

    Marque

    ELISA-VIDITEST

    Analytical Method

    Semi-Quantitative

    Ingrédients

    • ELISA break-away strips in the handling frame coated with the specific antigen STRIPS Ag 1 x 12 pcs
    • 1.3 mL of positive control human serum containing high avidity antibodies (High avidity control serum) r.t.u.1) HIGH AVID 1 vial
    • 1.3 mL of positive control human serum containing low avidity antibodies (Low avidity control serum) r.t.u. LOW AVID 1 vial
    • 1.3 mL Standard A = Negative control human serum, r.t.u. ST A/NC 1 vial
    • 2.0 mL Standard D = Calibrator (human serum), r.t.u. ST D/CAL 1 vial
    • / 1.3 mL Standard E = Positive control human serum, r.t.u. ST E/PC 1 vial
    • 13 mL Anti-human IgG animal antibodies labelled with horseradish peroxidase (anti-IgG Px conjugate) r.t.u. CONJ 1 vial
    • 55 mL Wash buffer, 10x concentrated WASH 10x 1 vial
    • 60 mL Dilution buffer, r.t.u. DIL 1 vial
    • 13 mL Chromogenic substrate TMB, r.t.u. (TMB/H2O2) TMB 1 vial
    • 13 mL Urea solution, r.t.u. UREA 1 vial
    • 13 mL Stop solution, r.t.u. (0.4 M sulfuric acid) STOP 1 vial
    • Instruction manual
    • Quality Control Certificate
    • 1) r.t.u., ready to use

    Matériel non inclus

    • Distilled or deionised water for dilution of buffer and standard concentrates
    • appropriate and calibrated equipment for pipetting
    • temperature controlled incubator
    • spectrophotometer or platereader with the appropriate filters
    • empty microtiter plate for pre-incubation
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Plaque

    Pre-coated

    Protocole

    anti-TBEV IgG and IgG avidity is a solid-phase immunoanalytical test. The polystyrene strips are coated with specific antigen which bear immunodominant epitopes of TBEV. Anti-TBEV antibodies in samples bind to the immobilized antigens. The antibodies that do not bind are washed away and those that formed complexes with the antigens are later on recognised by animal anti-human IgG antibodies labelled with horseradish peroxidase. The presence of labelled antibodies is revealed by an enzymatic reaction with a chromogenic substrate. Negative samples do not react and the mild change in colour, if present, may be attributed to the reaction background. To determine avidity, each sample is applied in parallel to two wells, with the appropriate antibodies binding to the immobilized antigens. In the next step, one well is incubated with the wash solution, the other well with the urea solution. In the first well, specific antibodies with high and low avidity remain bound to the antigen. In the second well, low-avidity antibodies are released due to the concentrated urea solution, and only high-avidity antibodies remain complex with the antigen. The ratio between the optical density of the well with the urea solution and the well with the washing solution in percent expresses the relative avidity index (RAI).

    Restrictions

    For Research Use only
  • Stock

    4 °C
  • Antigène

    Tick-Borne Encephalitis Virus IgG and IgG Avidity

    Classe de substances

    Antibody
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