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ALDH3A2 Antikörper (C-Term)

ALDH3A2 Reaktivität: Human, Maus WB, ELISA Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN6990973
  • Target Alle ALDH3A2 Antikörper anzeigen
    ALDH3A2 (Aldehyde Dehydrogenase 3 Family, Member A2 (ALDH3A2))
    Bindungsspezifität
    • 15
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    C-Term
    Reaktivität
    • 49
    • 10
    • 8
    • 6
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Human, Maus
    Wirt
    • 33
    • 15
    • 1
    Kaninchen
    Klonalität
    • 35
    • 14
    Polyklonal
    Konjugat
    • 25
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser ALDH3A2 Antikörper ist unkonjugiert
    Applikation
    • 48
    • 22
    • 19
    • 13
    • 13
    • 10
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), ELISA
    Spezifität
    At least four isoforms of Aldh3A2 are known to exist. This antibody is predicted to have no cross-reactivity to Aldh3A1.
    Aufreinigung
    Aldh3A2 Antibody is affinity chromatography purified via peptide column.
    Immunogen
    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.
    Isotyp
    IgG
    Top Product
    Discover our top product ALDH3A2 Primärantikörper
  • Applikationshinweise
    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.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 mg/mL
    Buffer
    Aldh3A2 Antibody is supplied in PBS containing 0.02 % sodium azide.
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    -20 °C,4 °C
    Informationen zur Lagerung
    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.
  • Target
    ALDH3A2 (Aldehyde Dehydrogenase 3 Family, Member A2 (ALDH3A2))
    Andere Bezeichnung
    Aldh3A2 (ALDH3A2 Produkte)
    Synonyme
    ALDH10 antikoerper, FALDH antikoerper, SLS antikoerper, AI194803 antikoerper, Ahd-3 antikoerper, Ahd-3r antikoerper, Ahd3 antikoerper, Ahd3-r antikoerper, Aldh4 antikoerper, Aldh4-r antikoerper, ALDH-III antikoerper, CG11140 antikoerper, CT41571 antikoerper, Dhap antikoerper, Dmel\\CG11140 antikoerper, l(2)03610 antikoerper, Aldh-III antikoerper, aldh3a2 antikoerper, wu:fc06b11 antikoerper, zgc:92064 antikoerper, ALDH3A2 antikoerper, aldehyde dehydrogenase 3 family member A2 antikoerper, aldehyde dehydrogenase family 3, subfamily A2 antikoerper, aldehyde dehydrogenase 3 family, member A2 antikoerper, Aldehyde dehydrogenase type III antikoerper, fatty aldehyde dehydrogenase antikoerper, aldehyde dehydrogenase 3 family, member A2a antikoerper, aldehyde dehydrogenase 3 family member A2 S homeolog antikoerper, aldH antikoerper, ALDH3A2 antikoerper, Aldh3a2 antikoerper, Aldh-III antikoerper, PTRG_02589 antikoerper, aldh3a2 antikoerper, aldh3a2a antikoerper, aldh3a2.S antikoerper, aldH antikoerper
    Hintergrund
    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.
    Gen-ID
    224
    NCBI Accession
    NP_001026976
    UniProt
    P51648
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