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ALDH5A1 anticorps (AA 400-500)

Cet anticorps Lapin Polyclonal détecte spécifiquement ALDH5A1 dans WB. Il présente une réactivité envers Humain.
N° du produit ABIN7265542

Aperçu rapide pour ALDH5A1 anticorps (AA 400-500) (ABIN7265542)

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
  • 2
  • 1
Western Blotting (WB)
  • Épitope

    • 7
    • 7
    • 7
    • 5
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 400-500

    Fonction

    ALDH5A1 Rabbit pAb

    Séquence

    VSKGATVVTG GKRHQLGKNF FEPTLLCNVT QDMLCTHEET FGPLAPVIKF DTEEEAIAIA NAADVGLAGY FYSQDPAQIW RVAEQLEVGM VGVNEGLISS V

     Réactivité croisée

    Souris, Rat

    Attributs du produit

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogène

    A synthetic peptide corresponding to a sequence within amino acids 400-500 of human ALDH5A1 (NP_001071.1).

    Isotype

    IgG
  • Indications d'application

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    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

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

    Autre désignation

    ALDH5A1

    Sujet

    This protein belongs to the aldehyde dehydrogenase family of proteins. This gene encodes 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. Two transcript variants encoding distinct isoforms have been identified for this gene.,ALDH5A1,SSADH,SSDH,Signal Transduction,Endocrine & Metabolism,Mitochondrial metabolism,Mitochondrial markers,Amino acid metabolism,Lipid Metabolism,Neuroscience,ALDH5A1

    Poids moléculaire

    57kDa/58kDa

    ID gène

    7915

    UniProt

    P51649

    Pathways

    Monocarboxylic Acid Catabolic Process
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