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ALDH5A1 Antikörper (C-Term)

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch ALDH5A1 in WB und EIA. Er zeigt eine Reaktivität gegenüber Human.
Produktnummer ABIN356986

Kurzübersicht für ALDH5A1 Antikörper (C-Term) (ABIN356986)

Target

Alle ALDH5A1 Antikörper anzeigen
ALDH5A1 (Aldehyde Dehydrogenase 5 Family, Member A1 (ALDH5A1))

Reaktivität

  • 47
  • 9
  • 8
  • 2
  • 2
  • 2
  • 1
Human

Wirt

  • 41
  • 3
  • 3
Kaninchen

Klonalität

  • 46
  • 1
Polyklonal

Konjugat

  • 26
  • 4
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser ALDH5A1 Antikörper ist unkonjugiert

Applikation

  • 36
  • 25
  • 23
  • 9
  • 5
  • 4
  • 3
  • 1
  • 1
Western Blotting (WB), Enzyme Immunoassay (EIA)
  • Bindungsspezifität

    • 8
    • 7
    • 7
    • 4
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    C-Term

    Spezifität

    This antibody detects ALDH5A1 at C-term.

    Aufreinigung

    Affinity Purified

    Immunogen

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

    Isotyp

    Ig Fraction
  • Applikationshinweise

    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.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    0.25 mg/mL

    Handhabung

    Avoid repeated freezing and thawing.

    Lagerung

    4 °C/-20 °C

    Informationen zur Lagerung

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

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

    Andere Bezeichnung

    ALDH5A1 / SSADH

    Hintergrund

    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

    Molekulargewicht

    57215 Da

    Gen-ID

    7915, 9606

    UniProt

    P51649

    Pathways

    Monocarboxylic Acid Catabolic Process
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