Epstein-Barr Virus VCA IgG and IgG Avidity Kit ELISA
Le kit ELISA Epstein-Barr Virus VCA IgG and IgG Avidity (ABIN459378) Humain est un kit ELISA Colorimetric conçu pour quantifier Humain Epstein-Barr Virus VCA IgG and IgG Avidity.
Aperçu rapide pour Epstein-Barr Virus VCA IgG and IgG Avidity Kit ELISA (ABIN459378)
Antigène
Epstein-Barr Virus VCA IgG and IgG Avidity
Reactivité
Humain
Méthode de détection
Colorimetric
Type de méthode
Indirect ELISA
Application
ELISA
Type d'échantillon
Serum, Plasma
Fonction
anti-VCA EBV 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-VCA EBV IgG and IgG avidity is a solid-phase immunoanalytical test. A specific antigen representing immunodominant epitopes of the VCA complex is bound to the surface of the wells. If antibodies are present in the test samples, they will bind to the immobilized proteins. The bound antibodies then react in the next step with horseradish peroxidase-labeled anti-human IgG antibodies. The amount of bound labeled antibodies is determined by a color enzymatic reaction. Negative samples do not react, a slight change in the color of the wells is the background of the reaction. 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).