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FGF13 Kit ELISA

Le kit ELISA FGF13 (ABIN4969095) Souris est un kit ELISA Colorimetric conçu pour quantifier Souris FGF13.
N° du produit ABIN4969095
1.308,08 €
Plus frais de livraison 40,00 € et TVA
96 tests
Destination: France
Envoi sous 7 à 15 jours ouvrables

Aperçu rapide pour FGF13 Kit ELISA (ABIN4969095)

Antigène

Voir toutes FGF13 Kits ELISA
FGF13 (Fibroblast Growth Factor 13 (FGF13))

Reactivité

  • 14
  • 7
  • 7
Souris

Méthode de détection

Colorimetric

Type de méthode

Sandwich ELISA

Gamme de detection

31.2 pg/mL - 2000 pg/mL

Application

ELISA

Type d'échantillon

Plasma, Serum

Classe de qualité

Small Sample
  • Seuil minimal de détection

    31.2 pg/mL

    Fonction

    This kit is based on sandwich enzyme-linked immuno-sorbent assay technology.

    Analytical Method

    Quantitative

    Sensibilité

    < 11.4 pg/mL

    Ingrédients

    The kit components listed are for reference only. The product manual may differ slightly. The product should be used as stated on the product manual included and delivered together with the product.
    • Pre-coated 96-Well Microplate
    • Standard
    • Standard Diluent Buffer
    • Wash Buffer
    • Detection Reagent A
    • Detection Reagent B
    • Diluent A
    • Diluent B
    • TMB Substrate
    • Stop Solution
    • Plate Sealer

    Matériel non inclus

    • 37 °C incubator
    • Multi and single channel pipettes and sterile pipette tips
    • Squirt bottle or automated microplate washer
    • 1.5 mL tubes
    • Distilled water
    • Absorbent filter papers
    • 100 mL and 1 liter graduated cylinders
    • Microplate reader (wavelength: 450 nm)
    • ELISA Shaker
  • Volume d'échantillon

    25 µL

    Plaque

    Pre-coated

    Protocole

    This kit is based on sandwich enzyme-linked immuno-sorbent assay technology. An antibody is pre-coated onto a 96-well plate. Standards, test samples, and biotin-conjugated reagent are added to the wells and incubated. The HRP-conjugated reagent is then added, and the whole plate is incubated. Unbound conjugates are removed using wash buffer at each stage. TMB substrate is used to quantify the HRP enzymatic reaction. After TMB substrate is added, only wells that contain sufficient FGF13 will produce a blue coloured product, which then changes to yellow after adding the acidic stop solution. The intensity of the yellow colour is proportional to the FGF13 amount bound on the plate. The Optical Density (OD) is measured spectrophotometrically at 450 nm in a microplate reader, from which the concentration of FGF13 can be calculated.

    Préparation des réactifs

    This procedure is provided for reference only. The product manual may differ slightly. The product should be used as stated on the product manual included and delivered together with the product.

    • 1) Standard: Prepare the standard with the recommended volume of Standard Diluent Buffer, to make the standard solution. Then use the Standard Diluent buffer to carry out serial dilutions of the standard solution, as instructed in the Protocol.
    • 2) Wash Buffer: Dilute the concentrated Wash Buffer with distilled water, as instructed in the Protocol.
    • 3) Detection Reagent Preparation: Calculate the total volume of working solution required. Dilute Detection Reagent A and Detection Reagent B with Diluent A and Diluent B, respectively, at 1:100.

    Procédure de l'essai

    This procedure is provided for reference only. The product manual may differ slightly. The product should be used as stated on the product manual included and delivered together with the product.

    • 1) Set standard, test samples and control wells.
    • 2) Aliquot 25 μL of diluted standard into the standard wells.
    • 3) Aliquot 25 μL of Standard Diluent buffer into control (zero) well.
    • 4) Aliquot 25 μL of diluted samples into the sample wells. Incubate for 1 hr at 37 °C.
    • 5) Aliquot 25 μL of Detection Reagent A to each well. Incubate for 1 hr at 37 °C.
    • 6) Wash 3 times.
    • 7) Aliquot 25 μL of Detection Reagent B to each well. Incubate for 30 mins at 37 °C.
    • 8) Wash 5 times.
    • 9) Aliquot 25 μL of TMB Substrate to each well. Incubate for 10-20 mins at 37 °C.
    • 10) Aliquot 20 μL of Stop Solution.
    • 11) Measure the OD at 450 nm.

    Calcul des résultats

    For calculation, average the O.D.450 duplicate readings for each reference standard and each sample and substract the average control (zero) O.D.450 reading. The standard curve can be plotted as the relative O.D.450 of each reference standard solution [Y] vs. the respective concentration of each standard solution (X). The FGF13 concentration of the samples can be interpolated from the standard curve.

    Précision du teste

    Intra-assay Precision (Precision within an assay): 3 samples with low, medium and high levels of Fibroblast Growth Factor 13 (FGF13) were were tested 20 times on one plate, respectively.

    Inter-assay Precision (Precision between assays): 3 samples with low, medium and high levels of Fibroblast Growth Factor 13 (FGF13) were tested on 3 different plates, 8 replicates in each plate.

    CV (%) = (Standard Deviation / mean) x 100

    Intra-Assay: CV<10%

    Inter-Assay: CV<12%

    Restrictions

    For Research Use only
  • Stock

    4 °C

    Stockage commentaire

    Shipped at 4°C. Upon receipt, store the kit according to the storage instruction in the kit's manual.The stability of the kit is determined by the rate of activity loss. The loss rate is less than 5% within the expiration date under appropriate storage conditions. To minimize performance fluctuations, operation procedures and lab conditions should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same user throughout.

    Date de péremption

    6 months
  • Antigène Voir toutes FGF13 Kits ELISA

    FGF13 (Fibroblast Growth Factor 13 (FGF13))

    Autre désignation

    Fibroblast Growth Factor 13

    ID gène

    14168

    UniProt

    P70377

    Pathways

    Regulation of Cell Size
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