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GNS anticorps (AA 174-203)

L’anticorps Lapin Polyclonal anti-GNS a été validé pour WB et IHC (p). Il convient pour détecter GNS dans des échantillons de Humain.
N° du produit ABIN390494

Aperçu rapide pour GNS anticorps (AA 174-203) (ABIN390494)

Antigène

Voir toutes GNS Anticorps
GNS (Glucosamine (N-Acetyl)-6-Sulfatase (GNS))

Reactivité

  • 32
  • 8
  • 6
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
Humain

Hôte

  • 29
  • 3
  • 1
Lapin

Clonalité

  • 32
  • 1
Polyclonal

Conjugué

  • 19
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp GNS est non-conjugé

Application

  • 16
  • 13
  • 13
  • 11
  • 6
  • 4
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone

RB19340
  • Épitope

    • 15
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 174-203

    Homologie

    B, M

    Purification

    This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.

    Immunogène

    This GNS antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 174-203 amino acids from the Central region of human GNS.

    Isotype

    Ig Fraction
  • Indications d'application

    WB: 1:1000. IHC-P: 1:50~100

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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

    4 °C,-20 °C

    Stockage commentaire

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    Date de péremption

    6 months
  • Antigène

    GNS (Glucosamine (N-Acetyl)-6-Sulfatase (GNS))

    Autre désignation

    GNS

    Sujet

    GNS is a lysosomal enzyme found in all cells. It is involved in the catabolism of heparin, heparan sulphate, and keratan sulphate. Deficiency of this enzyme results in the accumulation of undegraded substrate and the lysosomal storage disorder mucopolysaccharidosis type IIID (Sanfilippo D syndrome). Mucopolysaccharidosis type IIID is the least common of the four subtypes of Sanfilippo syndrome.

    Poids moléculaire

    62082

    ID gène

    2799

    NCBI Accession

    NP_002067

    UniProt

    P15586

    Pathways

    Glycosaminoglycan Metabolic Process
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