Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

IL-7 Kit ELISA

Ce kit ELISA Humain IL-7 est un kit ELISA Colorimetric conçu pour quantifier Humain IL-7.
N° du produit ABIN2112003

Aperçu rapide pour IL-7 Kit ELISA (ABIN2112003)

Antigène

Voir toutes IL-7 (IL7) Kits ELISA
IL-7 (IL7) (Interleukin 7 (IL7))

Reactivité

  • 10
  • 8
  • 7
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Humain

Méthode de détection

Colorimetric

Type de méthode

Sandwich ELISA

Gamme de detection

1.5-500 pg/mL

Application

ELISA
  • Seuil minimal de détection

    1.5 pg/mL

    Sensibilité

    < 1 pg/mL

    Ingrédients

    IL-7 MICROTITER PLATE
    BIOTIN CONJUGATE
    AVIDIN CONJUGATE
    IL-7 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 IL-7 ELISA is a ready-to-use 3.5-hour solid phase immunoassay readily capable of measuring IL-7 levels in serum, plasma, cell culture supernatant, and other biological fluids in the range of 0 to 2000pg/ml. This assay has shown no cross-reactivity with other cytokines tested, and is expected to be used effectively for further investigations into the relationship between IL-7 and the various conditions mentioned.This IL-7 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 IL-7. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated polyclonal antibody preparation specific for IL-7 and incubated. If present, IL-7 will bind and become immobilized by the antibody pre-coated on the wells and then become -sandwiched- by biotin conjugate. The microtiter plate wells are thoroughly washed to remove unbound IL- 7 and other components of the sample. In order to quantitatively determine the amount of IL-7 present 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, each having a high affinity-binding site for biotin. The wells are thoroughly washed to remove all unbound HRP-conjugated Avidin and a TMB (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 IL-7, 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 IL-7 (IL7) Kits ELISA

    IL-7 (IL7) (Interleukin 7 (IL7))

    Autre désignation

    Interleukin-7

    Pathways

    Signalistation JAK/STAT
Vous êtes ici:
Chat with us!