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IDS Kit ELISA

Kit ELISA IDS Humain, Colorimetric test pour la quantification de Humain IDS.
N° du produit ABIN3044712
918,50 €
Plus frais de livraison 40,00 € et TVA
96 tests
Destination: France
Envoi sous 8 à 12 jours ouvrables

Aperçu rapide pour IDS Kit ELISA (ABIN3044712)

Antigène

Voir toutes IDS Kits ELISA
IDS (Iduronate 2-Sulfatase (IDS))

Épitope

AA 26-550

Reactivité

  • 15
  • 7
  • 2
  • 1
  • 1
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Humain

Méthode de détection

Colorimetric

Type de méthode

Sandwich ELISA

Gamme de detection

156 pg/mL - 10000 pg/mL

Application

ELISA

Type d'échantillon

Cell Culture Supernatant, Cell Lysate, Plasma (EDTA), Plasma (heparin), Serum
  • Seuil minimal de détection

    156 pg/mL

    Fonction

    Sandwich Human IDS/Iduronate 2 Sulfatase ELISA Kit to quantitate Human IDS in cell culture supernatants, cell lysates, serum and plasma (heparin, EDTA).

    Analytical Method

    Quantitative

    Specificité

    Expression system for standard: NS0
    Immunogen sequence: S26-P550

    Capture antibody and Detection antibody: polyclonal antibody from goat, a biotinylated polyclonal antibody from goat

    Réactivité croisée (Details)

    There is no detectable cross-reactivity with other relevant proteins.

    Sensibilité

    < 15 pg/mL

    Ingrédients

    1. Pre-coated 96-well strip microplate
    2. Standard
    3. Biotinylated antibody (100x)
    4. Avidin-Biotin-Peroxidase Complex (100x)
    5. Sample Diluent
    6. Antibody Diluent
    7. Avidin-Biotin-Peroxidase Diluent
    8. Color Developing Reagent (TMB)
    9. Stop Solution
    10. Wash Buffer (25x)
    11. Adhesive plate sealers

    Matériel non inclus

    Microplate Reader capable of reading absorbance at 450nm. Incubator. Automated plate washer (optional). Pipettes and pipette tips capable of precisely dispensing 0.5 μL through 1 mL volumes of aqueous solutions. Multichannel pipettes are recommended for large amount of samples. Deionized or distilled water. 500 mL graduated cylinders. Test tubes for dilution.
  • Indications d'application

    Before using Kit, spin tubes and bring down all components to bottom of tube. Duplicate well assay was recommended for both standard and sample testing.

    Volume d'échantillon

    100 μL

    Plaque

    Pre-coated

    Protocole

    ELISA Kit is based on standard sandwich enzyme-linked immune-sorbent assay technology. An antibody has been precoated onto 96-well plates. Standards and test samples are added to the wells, a biotinylated detection antibody specific for target is added subsequently and then followed by washing with PBS or TBS buffer. Avidin-Biotin-Peroxidase Complex was added and unbound conjugates were washed away with PBS or TBS buffer. HRP substrate TMB was used to visualize HRP enzymatic reaction. TMB was catalyzed by HRP to produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional to the target amount in sample captured in plate.

    Précision du teste

    Intra-Assay Precision (CV%): 6.8%, 4.2%, 7.8%
    Inter-Assay Precision (CV%): 8.1%, 5%, 9.6%

    Restrictions

    For Research Use only
  • Conseil sur la manipulation

    Avoid multiple freeze-thaw cycles.

    Stock

    4 °C,-20 °C

    Stockage commentaire

    Store at 4°C for 6 months, at -20°C for 12 months. Avoid multiple freeze-thaw cycles (Ships with gel ice, can store for up to 3 days in room temperature. Freeze upon receiving.)

    Date de péremption

    12 months
  • Antigène Voir toutes IDS Kits ELISA

    IDS (Iduronate 2-Sulfatase (IDS))

    Autre désignation

    IDS

    Sujet

    Background: Iduronate 2-sulfatase (IDS) is a sulfatase enzyme associated with Hunter syndrome. It encodes a member of the sulfatase family of proteins. Iduronate 2-sulfatase is involved in the lysosomal degradation of the glycosaminoglycans heparan sulfate and dermatan sulfate. The encoded preproprotein is proteolytically processed to generate two polypeptide chains. Mutations in this gene are associated with the X-linked lysosomal storage disease mucopolysaccharidosis type II, also known as Hunter syndrome. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed.

    Gene Full Name: iduronate 2-sulfatase

    ID gène

    3423

    UniProt

    P22304

    Pathways

    Glycosaminoglycan Metabolic Process
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