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).