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AASS anticorps (AA 37-865)

Cet anticorps Lapin Polyclonal détecte spécifiquement AASS dans WB, ELISA, IF, IHC (p) et FACS. Il présente une réactivité avec des échantillons de Humain, Souris et Rat.
N° du produit ABIN7874420
644,88 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour AASS anticorps (AA 37-865) (ABIN7874420)

Antigène

Voir toutes AASS Anticorps
AASS (Aminoadipate Semialdehyde Synthase (AASS))

Reactivité

  • 23
  • 7
  • 6
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
Humain, Souris, Rat

Hôte

  • 26
Lapin

Clonalité

  • 25
Polyclonal

Conjugué

  • 23
  • 1
  • 1
  • 1
Cet anticorp AASS est non-conjugé

Application

  • 21
  • 12
  • 9
  • 6
  • 4
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)
  • Épitope

    • 5
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 37-865

    Fonction

    AASS Antibody / LKR / SDH

    Purification

    Antigen affinity purified

    Immunogène

    Recombinant human protein (amino acids E37-N865) was used as the immunogen for the AASS antibody.

    Isotype

    IgG
  • Indications d'application

    Optimal dilution of the AASS antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Stock

    4 °C,-20 °C

    Stockage commentaire

    After reconstitution, the AASS antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Antigène

    AASS (Aminoadipate Semialdehyde Synthase (AASS))

    Autre désignation

    AASS

    Sujet

    Alpha-aminoadipic semialdehyde synthase (AASS), also called Lysine ketoglutarate reductase (LKR) and Saccharopine dehydrogenase (SDH) is an enzyme encoded by the AASS gene in humans and is involved in their major lysine degradation pathway. This gene encodes a bifunctional enzyme that catalyzes the first two steps in the mammalian lysine degradation pathway. The N-terminal and the C-terminal portions of this enzyme contain lysine-ketoglutarate reductase and saccharopine dehydrogenase activity, respectively, resulting in the conversion of lysine to alpha-aminoadipic semialdehyde. Mutations in this gene are associated with familial hyperlysinemia.

    UniProt

    Q9UDR5

    Pathways

    SARS-CoV-2 Protein Interactome
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