Ce kit ELISA Colorimetric est conçu pour la mesure quantitative de Humain .
N° du produit ABIN7666569
Aperçu rapide pour SARS-CoV-2 N-Protein IgA Antibody Kit ELISA (ABIN7666569)
Antigène
SARS-CoV-2 N-Protein IgA Antibody
Reactivité
Humain
Méthode de détection
Colorimetric
Type de méthode
Indirect ELISA
Application
ELISA
Type d'échantillon
Plasma, Serum
Fonction
anti-SARS-CoV-2 (NP) IgA - ELISA kit for the detection of IgA antibodies to nucleocapsid protein (NP) of coronavirus SARS-CoV-2, causing the COVID-19 disease in human serum and plasma isolated from venous or capillary blood.
Marque
ELISA-VIDITEST
Analytical Method
Semi-Quantitative
Ingrédients
ELISA break-away strips in the handling frame coated with the antigen STRIPS Ag 1 x 12 pcs
1.3 mL Negative control serum, r.t.u. NC 1 vial
1.3 mL Positive control serum, r.t.u. PC 1 vial
1.3 mL Calibrator, r.t.u. 1) CAL 1 vial
13 mL Anti-human IgA antibodies labelled with horseradish peroxidase (anti-IgA 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 1 vial
13 mL Stop solution, r.t.u. STOP 1 vial
Instruction manual
Certificate
of quality 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
Optimal working dilution should be determined by the investigator.
Plaque
Pre-coated
Protocole
anti-SARS-CoV-2 (NP) IgA is a solid-phase immunoanalytical test. The specific antigen (Nucleocapsid Protein) is fixed to each well of the microtiterstrips. Specific antibodies present in the patient's sample are bound during the first incubation step. After removing unbound material by washing, the presence of the specific antibodies is detected using anti-human IgA conjugate during the second incubation. The unbound peroxidase conjugate is then removed and TMB substrate is added, resulting in the development of a blue colour in positive samples. The enzyme reaction is terminated by addition of the stop solution (colour change to yellow). The intensity of the yellow colour thus developed is proportional to the concentration of antibodies in the sample. 2