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ALDH3A2 anticorps (C-Term)

ALDH3A2 Reactivité: Humain, Souris WB, ELISA Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN6990973
  • Antigène Voir toutes ALDH3A2 Anticorps
    ALDH3A2 (Aldehyde Dehydrogenase 3 Family, Member A2 (ALDH3A2))
    Épitope
    • 15
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    C-Term
    Reactivité
    • 49
    • 10
    • 8
    • 6
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Humain, Souris
    Hôte
    • 33
    • 15
    • 1
    Lapin
    Clonalité
    • 35
    • 14
    Polyclonal
    Conjugué
    • 25
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp ALDH3A2 est non-conjugé
    Application
    • 48
    • 22
    • 19
    • 13
    • 13
    • 10
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), ELISA
    Specificité
    At least four isoforms of Aldh3A2 are known to exist. This antibody is predicted to have no cross-reactivity to Aldh3A1.
    Purification
    Aldh3A2 Antibody is affinity chromatography purified via peptide column.
    Immunogène
    Aldh3A2 antibody was raised against a 14 amino acid synthetic peptide near the carboxy terminus of the human Aldh3A2. The immunogen is located within the last 50 amino acids of Aldh3A2.
    Isotype
    IgG
    Top Product
    Discover our top product ALDH3A2 Anticorps primaire
  • Indications d'application
    Aldh3A2 antibody can be used for detection of Aldh3A2 by Western blot at 1 - 2 μ,g/mL.

    Antibody validated: Western Blot in mouse samples. All other applications and species not yet tested.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    Aldh3A2 Antibody is supplied in PBS containing 0.02 % sodium azide.
    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,4 °C
    Stockage commentaire
    Aldh3A2 antibody can be stored at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
  • Antigène
    ALDH3A2 (Aldehyde Dehydrogenase 3 Family, Member A2 (ALDH3A2))
    Autre désignation
    Aldh3A2 (ALDH3A2 Produits)
    Synonymes
    anticorps ALDH10, anticorps FALDH, anticorps SLS, anticorps AI194803, anticorps Ahd-3, anticorps Ahd-3r, anticorps Ahd3, anticorps Ahd3-r, anticorps Aldh4, anticorps Aldh4-r, anticorps ALDH-III, anticorps CG11140, anticorps CT41571, anticorps Dhap, anticorps Dmel\\CG11140, anticorps l(2)03610, anticorps Aldh-III, anticorps aldh3a2, anticorps wu:fc06b11, anticorps zgc:92064, anticorps ALDH3A2, anticorps aldehyde dehydrogenase 3 family member A2, anticorps aldehyde dehydrogenase family 3, subfamily A2, anticorps aldehyde dehydrogenase 3 family, member A2, anticorps Aldehyde dehydrogenase type III, anticorps fatty aldehyde dehydrogenase, anticorps aldehyde dehydrogenase 3 family, member A2a, anticorps aldehyde dehydrogenase 3 family member A2 S homeolog, anticorps aldH, anticorps ALDH3A2, anticorps Aldh3a2, anticorps Aldh-III, anticorps PTRG_02589, anticorps aldh3a2, anticorps aldh3a2a, anticorps aldh3a2.S, anticorps aldH
    Sujet
    Aldh3A2 Antibody: Aldh3A2 is a member of the aldehyde dehydrogenase superfamily, a group of NAD(P)(+)-dependent enzymes that catalyze the oxidation of a wide spectrum of aliphatic and aromatic aldehydes. Aldehyde dehydrogenase enzymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. Aldh3A2 catalyzes the oxidation of long-chain aliphatic aldehydes to fatty acids. Mutations in the Aldh3A2 gene cause Sjogren-Larrson syndrome, an inherited neurocutaneous disorder. Patients with this disorder display ichthyosis, mental retardation and spastic diplegia. The pathogenesis of the cutaneous and neurological symptoms is thought to result from abnormal lipid accumulation in the membranes of skin and brain, the formation of aldehyde Schiff base adducts with amine-containing lipids or proteins, or defective eicosanoid metabolism.
    ID gène
    224
    NCBI Accession
    NP_001026976
    UniProt
    P51648
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