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

IDS Kit ELISA

Kit ELISA Humain IDS, test Colorimetric pour la quantification de Humain IDS.
N° du produit ABIN3044712

Aperçu rapide pour IDS Kit ELISA (ABIN3044712)

Antigène

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

Épitope

AA 26-550

Reactivité

  • 6
  • 5
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Humain

Méthode de détection

Colorimetric

Type de méthode

Sandwich ELISA

Gamme de detection

156-10000 pg/mL

Application

ELISA

Type d'échantillon

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

    156 pg/mL

    Fonction

    Sandwich High Sensitivity ELISA kit for Quantitative Detection of Human IDS

    Marque

    PicoKine™

    Analytical Method

    Quantitative

    Specificité

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

    Réactivité croisée (Details)

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

    Sensibilité

    <15pg/mL

    Matériel non inclus

    Microplate reader in standard size. Automated plate washer. Adjustable pipettes and pipette tips. Multichannel pipettes are recommended in the condition of large amount of samples in the detection. Clean tubes and Eppendorf tubes. Washing buffer (neutral PBS or TBS). Preparation of 0.01M TBS: Add 1.2g Tris, 8.5g Nacl

    Immunogène

    Immunogen sequence: S26-P550
  • 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.

    Commentaires

    Tissue Specificity: Liver, kidney, lung, and placenta.

    Plaque

    Pre-coated

    Protocole

    human IDS ELISA Kit was based on standard sandwich enzyme-linked immune-sorbent assay technology. A monoclonal antibody from mouse specific for IDS has been precoated onto 96-well plates. Standards(Expression system for standard: NSO, Immunogen sequence: S26-P550) and test samples are added to the wells, a biotinylated detection polyclonal antibody from goat specific for IDS 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 human IDS amount of sample captured in plate.

    Procédure de l'essai

    Aliquot 0.1 mL per well of the 10000pg/mL, 5000pg/mL, 2500pg/mL, 1250pg/mL, 625pg/mL, 312pg/mL, 156pg/mL human IDS standard solutions into the precoated 96-well plate. Add 0.1 mL of the sample diluent buffer into the control well (Zero well). Add 0.1 mL of each properly diluted sample of human cell culture supernates, serum or plasma(heparin, EDTA) to each empty well. See "Sample Dilution Guideline" above for details. It is recommended that each human IDS standard solution and each sample be measured in duplicate.

    Restrictions

    For Research Use only
  • Buffer

    heparin or EDTA

    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

    Date de péremption

    12 months
  • Antigène Voir toutes IDS Kits ELISA

    IDS (Iduronate 2-Sulfatase (IDS))

    Autre désignation

    IDS

    Sujet

    Protein Function: Required for the lysosomal degradation of heparan sulfate and dermatan sulfate.

    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.

    Synonyms: Iduronate 2-sulfatase,3.1.6.13,Alpha-L-iduronate sulfate sulfatase,Idursulfase,Iduronate 2-sulfatase 42 kDa chain,Iduronate 2-sulfatase 14 kDa chain,IDS,SIDS,

    Full Gene Name: Iduronate 2-sulfatase

    Cellular Localisation: Lysosome.

    ID gène

    3423

    UniProt

    P22304

    Pathways

    Glycosaminoglycan Metabolic Process
Vous êtes ici:
Chat with us!