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AGLU anticorps (N-Term)

Cet anticorps Lapin Polyclonal détecte spécifiquement AGLU dans WB, EIA et IHC (p). Il présente une réactivité envers Humain.
N° du produit ABIN950380

Aperçu rapide pour AGLU anticorps (N-Term) (ABIN950380)

Antigène

Voir toutes AGLU Anticorps
AGLU (alpha-Glucosidase (AGLU))

Reactivité

  • 9
  • 6
  • 1
  • 1
Humain

Hôte

  • 10
  • 5
Lapin

Clonalité

  • 10
  • 5
Polyclonal

Conjugué

  • 12
  • 3
Cet anticorp AGLU est non-conjugé

Application

  • 15
  • 6
  • 6
  • 5
  • 4
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB), Enzyme Immunoassay (EIA), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Épitope

    • 1
    • 1
    • 1
    • 1
    AA 173-203, N-Term

    Specificité

    This antibody recognizes Human Alpha-glucosidase (N-term).

    Purification

    Protein A column, followed by peptide affinity purification

    Immunogène

    conjugated synthetic peptide between 173-203 amino acids from the N-terminal region of Human Alpha-glucosidase Genename: GAA

    Isotype

    Ig Fraction
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.25 mg/mL

    Buffer

    PBS containing 0.09 % (W/V) Sodium Azide as preservative

    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.

    Conseil sur la manipulation

    Avoid repeated freezing and thawing.

    Stock

    4 °C/-20 °C

    Stockage commentaire

    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Antigène

    AGLU (alpha-Glucosidase (AGLU))

    Autre désignation

    alpha-Glucosidase

    Sujet

    This gene encodes acid alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. Different forms of acid alpha-glucosidase are obtained by proteolytic processing. Defects in this gene are the cause of glycogen storage disease II, also known as Pompe's disease, which is an autosomal recessive disorder with a broad clinical spectrum. Three transcript variants encoding the same protein have been found for this gene.Synonyms: Acid maltase, Aglucosidase alfa, GAA, LYAG, Lysosomal alpha-glucosidase

    Poids moléculaire

    105319 Da

    ID gène

    2548

    NCBI Accession

    NP_000143

    Pathways

    Cellular Glucan Metabolic Process
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