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ALDH5A1 antibody

ALDH5A1 Reactivity: Human, Rat, Mouse ELISA, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7238516
  • Target See all ALDH5A1 Antibodies
    ALDH5A1 (Aldehyde Dehydrogenase 5 Family, Member A1 (ALDH5A1))
    Reactivity
    • 58
    • 8
    • 7
    • 2
    • 2
    • 2
    • 1
    Human, Rat, Mouse
    Host
    • 52
    • 3
    • 3
    Rabbit
    Clonality
    • 57
    • 1
    Polyclonal
    Conjugate
    • 27
    • 6
    • 6
    • 5
    • 4
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This ALDH5A1 antibody is un-conjugated
    Application
    • 47
    • 32
    • 31
    • 14
    • 6
    • 3
    • 2
    • 2
    • 1
    ELISA, Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Synthetic peptide of human ALDH5A1
    Isotype
    IgG
    Top Product
    Discover our top product ALDH5A1 Primary Antibody
  • Application Notes
    IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.5 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    ALDH5A1 (Aldehyde Dehydrogenase 5 Family, Member A1 (ALDH5A1))
    Alternative Name
    ALDH5A1 (ALDH5A1 Products)
    Synonyms
    SSADH antibody, SSDH antibody, Ssadh antibody, 6330403E24Rik antibody, Ahd-1 antibody, Ahd1 antibody, D630032B01Rik antibody, OTTMUSG00000000613 antibody, Ssdh1 antibody, aldehyde dehydrogenase 5 family member A1 antibody, aldehyde dehydrogenase 5 family, member A1 antibody, aldhehyde dehydrogenase family 5, subfamily A1 antibody, ALDH5A1 antibody, aldh5a1 antibody, Aldh5a1 antibody
    Background
    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.
    NCBI Accession
    NP_001071
    UniProt
    P51649
    Pathways
    Monocarboxylic Acid Catabolic Process
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