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ALDH4A1 antibody (AA 354-563)

The Rabbit Polyclonal anti-ALDH4A1 antibody has been validated for WB and IF. It is suitable to detect ALDH4A1 in samples from Human.
Catalog No. ABIN3023403

Quick Overview for ALDH4A1 antibody (AA 354-563) (ABIN3023403)

Target

See all ALDH4A1 Antibodies
ALDH4A1 (Aldehyde Dehydrogenase 4 Family, Member A1 (ALDH4A1))

Reactivity

  • 26
  • 11
  • 10
  • 4
  • 4
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 21
  • 5
Rabbit

Clonality

  • 24
  • 2
Polyclonal

Conjugate

  • 26
This ALDH4A1 antibody is un-conjugated

Application

  • 26
  • 16
  • 9
  • 5
  • 3
  • 2
  • 1
Western Blotting (WB), Immunofluorescence (IF)
  • Binding Specificity

    • 6
    • 5
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 354-563

    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
  • 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

    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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