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Interleukin 17a Kit ELISA

Ce kit ELISA Souris Interleukin 17a est un kit ELISA Colorimetric conçu pour quantifier Souris Interleukin 17a.
N° du produit ABIN2111994

Aperçu rapide pour Interleukin 17a Kit ELISA (ABIN2111994)

Antigène

Voir toutes Interleukin 17a (IL17A) Kits ELISA
Interleukin 17a (IL17A) (Interleukin 17A (IL17A))

Reactivité

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Souris

Méthode de détection

Colorimetric

Type de méthode

Sandwich ELISA

Gamme de detection

15.6-1000 pg/mL

Application

ELISA
  • Seuil minimal de détection

    15.6 pg/mL

    Sensibilité

    < 2 pg/mL

    Ingrédients

    ANTI-MOUSE IL-17A MICROTITER PLATE
    BIOTIN CONJUGATE
    AVIDIN CONJUGATE
    MOUSE IL-17 STANDARD
    CALIBRATOR DILUENT I
    CALIBRATOR DILUENT II
    WASH BUFFER (20X/96 wells, 30X/192 wells)
    SUBSTRATE A
    SUBSTRATE B
    STOP SOLUTION
  • Plaque

    Pre-coated

    Protocole

    This mouse IL-17A ELISA is a 3.5-hour solid phase immunoassay readily applicable to measure mouse IL-17A levels in cell culture supernatant and mouse serum in the range of 0 to 1000pg/ml. It showed no cross reactivity with other cytokines tested. This mouse IL-17A ELISA is expected to be effectively used for further investigations into the relationship between IL-17A and the various conditions mentioned. This mouse IL-17A enzyme linked immunosorbent assay (ELISA) applies a technique called a quantitative sandwich immunoassay. The microtiter plate provided in this kit has been pre-coated with a monoclonal antibody specific to mouse IL-17A. Standards or samples are then added to the appropriate microtiter plate wells. A biotin-conjugated antibody preparation specific for mouse IL-17A was added and incubated. Mouse IL-17A, if present, will bind and become immobilized by the antibody pre-coated on the wells. The microtiter plate wells are thoroughly washed to remove unbound mouse IL-17A and other components in the sample. Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Avidin is a tetramer containing four identical subunits that each has a high affinity-binding site for biotin. The wells are thoroughly washed to remove all unbound HRP-conjugated Avidin, and aTMB(3,3'5, 5' tetramethyl-benzidine) substrate solution is added to each well. The enzyme (HRP) and substrate are allowed to react over a short incubation period. Only those wells that contain mouse IL-17A, 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 450nm ± 2nm.

    Restrictions

    For Research Use only
  • Stock

    4 °C/-20 °C
  • Antigène Voir toutes Interleukin 17a (IL17A) Kits ELISA

    Interleukin 17a (IL17A) (Interleukin 17A (IL17A))

    Autre désignation

    Interleukin-17A
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