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ALDH5A1 antibody (AA 400-500)

This Rabbit Polyclonal antibody specifically detects ALDH5A1 in WB. It exhibits reactivity toward Human.
Catalog No. ABIN7265542

Quick Overview for ALDH5A1 antibody (AA 400-500) (ABIN7265542)

Target

See all ALDH5A1 Antibodies
ALDH5A1 (Aldehyde Dehydrogenase 5 Family, Member A1 (ALDH5A1))

Reactivity

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

Host

  • 41
  • 3
  • 3
Rabbit

Clonality

  • 46
  • 1
Polyclonal

Conjugate

  • 26
  • 4
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This ALDH5A1 antibody is un-conjugated

Application

  • 36
  • 25
  • 23
  • 9
  • 5
  • 4
  • 3
  • 2
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 8
    • 7
    • 7
    • 5
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 400-500

    Purpose

    ALDH5A1 Rabbit pAb

    Sequence

    VSKGATVVTG GKRHQLGKNF FEPTLLCNVT QDMLCTHEET FGPLAPVIKF DTEEEAIAIA NAADVGLAGY FYSQDPAQIW RVAEQLEVGM VGVNEGLISS V

    Cross-Reactivity

    Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

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

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    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

    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.,ALDH5A1,SSADH,SSDH,Signal Transduction,Endocrine & Metabolism,Mitochondrial metabolism,Mitochondrial markers,Amino acid metabolism,Lipid Metabolism,Neuroscience,ALDH5A1

    Molecular Weight

    57kDa/58kDa

    Gene ID

    7915

    UniProt

    P51649

    Pathways

    Monocarboxylic Acid Catabolic Process
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