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IDS anticorps

Cet anticorps anti-IDS Polyclonal Lapin (ABIN8122144) détecte spécifiquement IDS dans WB et ELISA. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.
N° du produit ABIN8122144
450,00 €
Plus frais de livraison 40,00 € et TVA
50 μL
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour IDS anticorps (ABIN8122144)

Antigène

Voir toutes IDS Anticorps
IDS (Iduronate 2-Sulfatase (IDS))

Reactivité

  • 56
  • 10
  • 8
  • 3
  • 3
  • 2
  • 2
  • 2
Humain, Souris, Rat

Hôte

  • 46
  • 11
  • 3
Lapin

Clonalité

  • 52
  • 8
Polyclonal

Conjugué

  • 35
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp IDS est non-conjugé

Application

  • 46
  • 22
  • 13
  • 13
  • 12
  • 10
  • 8
  • 6
  • 3
  • 2
  • 1
Western Blotting (WB), ELISA
  • Fonction

    IDS Antibody

    Specificité

    IDS Polyclonal Antibody detects endogenous levels of protein.

    Purification

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

    Immunogène

    Synthesized peptide derived from part region of human protein

    Isotype

    IgG
  • Indications d'application

    WB 1:500-2000 ELISA 1:5000-20000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Liquid in PBS containing 50 % glycerol, and 0.02 % sodium azide.

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    -20 °C

    Stockage commentaire

    Store at -20°C/1 year

    Date de péremption

    12 months
  • Antigène

    IDS (Iduronate 2-Sulfatase (IDS))

    Autre désignation

    IDS

    Sujet

    Background: This gene encodes a member of the sulfatase family of proteins. The encoded preproprotein is proteolytically processed to generate two polypeptide chains. This enzyme is involved in the lysosomal degradation of heparan sulfate and dermatan sulfate. 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. [provided by RefSeq, Jan 2016],

    Gene Name: IDS SIDS

    Protein Name: Iduronate 2-sulfatase (EC 3.1.6.13) (Alpha-L-iduronate sulfate sulfatase) (Idursulfase) [Cleaved into: Iduronate 2-sulfatase 42 kDa chainIduronate 2-sulfatase 14 kDa chain]

    ID gène

    3423

    UniProt

    P22304

    Pathways

    Glycosaminoglycan Metabolic Process
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