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SGSH anticorps

SGSH Reactivité: Humain, Rat, Souris IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7264201
  • Antigène Voir toutes SGSH Anticorps
    SGSH (N-Sulfoglucosamine Sulfohydrolase (SGSH))
    Reactivité
    • 31
    • 18
    • 5
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Humain, Rat, Souris
    Hôte
    • 43
    • 3
    • 1
    Lapin
    Clonalité
    • 46
    • 1
    Polyclonal
    Conjugué
    • 22
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp SGSH est non-conjugé
    Application
    • 46
    • 17
    • 13
    • 13
    • 6
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein of human SGSH (NP_000190.1).
    Isotype
    IgG
    Top Product
    Discover our top product SGSH Anticorps primaire
  • Indications d'application
    IHC 1:50-1:100
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    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. Avoid freeze / thaw cycles.
  • Antigène
    SGSH (N-Sulfoglucosamine Sulfohydrolase (SGSH))
    Autre désignation
    SGSH (SGSH Produits)
    Synonymes
    anticorps HSS, anticorps MPS3A, anticorps SFMD, anticorps 4632406A19Rik, anticorps N-sulfoglucosamine sulfohydrolase, anticorps N-sulfoglucosamine sulfohydrolase (sulfamidase), anticorps SGSH, anticorps Sgsh
    Sujet
    This gene encodes one of several enzymes involved in the lysosomal degradation of heparan sulfate. Mutations in this gene are associated with Sanfilippo syndrome A, one type of the lysosomal storage disease mucopolysaccaridosis III, which results from impaired degradation of heparan sulfate. Transcripts of varying sizes have been reported but their biological validity has not been determined.
    ID gène
    6448
    UniProt
    P51688
    Pathways
    Glycosaminoglycan Metabolic Process
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