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ALDH5A1 anticorps (C-Term)

Cet anticorps Lapin Polyclonal détecte spécifiquement ALDH5A1 dans WB et EIA. Il présente une réactivité envers Humain.
N° du produit ABIN356986

Aperçu rapide pour ALDH5A1 anticorps (C-Term) (ABIN356986)

Antigène

Voir toutes ALDH5A1 Anticorps
ALDH5A1 (Aldehyde Dehydrogenase 5 Family, Member A1 (ALDH5A1))

Reactivité

  • 46
  • 9
  • 8
  • 2
  • 2
  • 2
  • 1
Humain

Hôte

  • 40
  • 3
  • 3
Lapin

Clonalité

  • 45
  • 1
Polyclonal

Conjugué

  • 25
  • 4
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp ALDH5A1 est non-conjugé

Application

  • 35
  • 24
  • 22
  • 9
  • 4
  • 4
  • 3
  • 1
  • 1
Western Blotting (WB), Enzyme Immunoassay (EIA)
  • Épitope

    • 7
    • 7
    • 7
    • 4
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    C-Term

    Specificité

    This antibody detects ALDH5A1 at C-term.

    Purification

    Affinity Purified

    Immunogène

    This antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide selected from the C-terminal region of human ALDH5A1.

    Isotype

    Ig Fraction
  • Indications d'application

    ELISA 1: 1,000. Western blot 1: 50 - 1: 100. Immunohistochemistry 1: 10 - 1: 50.
    Other applications not tested.
    Optimal dilutions are dependent on conditions and should be determined by the user.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.25 mg/mL

    Conseil sur la manipulation

    Avoid repeated freezing and thawing.

    Stock

    4 °C/-20 °C

    Stockage commentaire

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

    ALDH5A1 (Aldehyde Dehydrogenase 5 Family, Member A1 (ALDH5A1))

    Autre désignation

    ALDH5A1 / SSADH

    Sujet

    ALDH5A1 belongs to the aldehyde dehydrogenase family of proteins. This protein functions as a mitochondrial NAD(+)-dependent succinic semialdehyde dehydrogenase. A deficiency of this enzyme, known as 4-hydroxybutyricaciduria, is a rare inborn error in the metabolism of the neurotransmitter 4-aminobutyric acid (GABA). In response to the defect, physiologic fluids from patients accumulate GHB, a compound with numerous neuromodulatory properties.Synonyms: Aldehyde dehydrogenase family 5 member A1, NAD(+)-dependent succinic semialdehyde dehydrogenase, Succinate-semialdehyde dehydrogenase, mitochondrial

    Poids moléculaire

    57215 Da

    ID gène

    7915, 9606

    UniProt

    P51649

    Pathways

    Monocarboxylic Acid Catabolic Process
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