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AGA anticorps (Middle Region)

AGA Reactivité: Humain WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN926652
  • Antigène Voir toutes AGA Anticorps
    AGA (Aspartylglucosaminidase (AGA))
    Épitope
    • 6
    • 1
    • 1
    • 1
    • 1
    • 1
    Middle Region
    Reactivité
    • 20
    • 11
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    Humain
    Hôte
    • 20
    • 1
    Lapin
    Clonalité
    • 21
    Polyclonal
    Conjugué
    • 10
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp AGA est non-conjugé
    Application
    • 11
    • 7
    • 4
    • 2
    • 2
    • 1
    Western Blotting (WB)
    Purification
    Purified
    Immunogène
    AGA antibody was raised in rabbit using the middle region of AGA as the immunogen
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    Discover our top product AGA Anticorps primaire
  • Indications d'application
    Optimal conditions should be determined by the investigator.
    Commentaires

    AGA Blocking Peptide, catalog no. 33R-10401, is also available for use as a blocking control in assays to test for specificity of this AGA antibody

    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Concentration
    Lot specific
    Buffer
    Lyophilized powder. Add 50 µL of distilled water. Final antibody concentration is 1 mg/mL in PBS buffer.
    Conseil sur la manipulation
    Avoid repeated freeze/thaw cycles.
    Stock
    4 °C/-20 °C
    Stockage commentaire
    Store at 4 °C, following reconstitution, aliquot and store at -20 °C.
  • Antigène
    AGA (Aspartylglucosaminidase (AGA))
    Autre désignation
    AGA (AGA Produits)
    Synonymes
    anticorps AGU, anticorps ASRG, anticorps GA, anticorps AW060726, anticorps aspartylglucosaminidase, anticorps AGA, anticorps Aga
    Sujet
    Aspartylglucosaminidase is involved in the catabolism of N-linked oligosaccharides of glycoproteins. It cleaves asparagine from N-acetylglucosamines as one of the final steps in the lysosomal breakdown of glycoproteins. The lysosomal storage disease aspartylglycosaminuria is caused by a deficiency in the AGA enzyme. Synonyms: Polyclonal AGA antibody, Anti-AGA antibody, aspartylglucosaminidase antibody, AGU antibody, ASRG antibody, GA antibody.
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