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ALDH4A1 antibody (AA 354-563)

ALDH4A1 Reactivity: Human WB, IF Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN3023403
  • Target See all ALDH4A1 Antibodies
    ALDH4A1 (Aldehyde Dehydrogenase 4 Family, Member A1 (ALDH4A1))
    Binding Specificity
    • 6
    • 5
    • 3
    • 2
    • 1
    • 1
    • 1
    AA 354-563
    Reactivity
    • 25
    • 11
    • 10
    • 4
    • 4
    • 3
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    Human
    Host
    • 20
    • 5
    Rabbit
    Clonality
    • 23
    • 2
    Polyclonal
    Conjugate
    • 25
    This ALDH4A1 antibody is un-conjugated
    Application
    • 25
    • 15
    • 8
    • 5
    • 3
    • 2
    • 1
    Western Blotting (WB), Immunofluorescence (IF)
    Sequence
    LYVPHSLWPQ IKGRLLEEHS RIKVGDPAED FGTFFSAVID AKSFARIKKW LEHARSSPSL TILAGGKCDD SVGYFVEPCI VESKDPQEPI MKEEIFGPVL SVYVYPDDKY KETLQLVDST TSYGLTGAVF SQDKDVVQEA TKVLRNAAGN FYINDKSTGS IVGQQPFGGA RASGTNDKPG GPHYILRWTS PQVIKETHKP LGDWSYAYMQ
    Cross-Reactivity
    Human, Mouse
    Characteristics
    Polyclonal Antibodies
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein containing a sequence corresponding to amino acids 354-563 of human ALDH4A1 (NP_003739.2).
    Isotype
    IgG
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    Discover our top product ALDH4A1 Primary Antibody
  • Application Notes
    WB,1:500 - 1:2000,IF,1:50 - 1:200
    Restrictions
    For Research Use only
  • 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
    ALDH4A1 (Aldehyde Dehydrogenase 4 Family, Member A1 (ALDH4A1))
    Alternative Name
    ALDH4A1 (ALDH4A1 Products)
    Background
    This protein belongs to the aldehyde dehydrogenase family of proteins. This enzyme is a mitochondrial matrix NAD-dependent dehydrogenase which catalyzes the second step of the proline degradation pathway, converting pyrroline-5-carboxylate to glutamate. Deficiency of this enzyme is associated with type II hyperprolinemia, an autosomal recessive disorder characterized by accumulation of delta-1-pyrroline-5-carboxylate (P5C) and proline. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene.,ALDH4A1,ALDH4,P5CD,P5CDh,Cancer,Signal Transduction,Endocrine & Metabolism,Mitochondrial metabolism,Mitochondrial markers,Amino acid metabolism,ALDH4A1
    Molecular Weight
    55 kDa/56 kDa/61 kDa
    Gene ID
    8659
    UniProt
    P30038
    Pathways
    Monocarboxylic Acid Catabolic Process
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