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ACSL4 antibody (AA 28-56)

This Rabbit Polyclonal antibody specifically detects ACSL4 in WB and ELISA. It exhibits reactivity toward Human.
Catalog No. ABIN5647455

Quick Overview for ACSL4 antibody (AA 28-56) (ABIN5647455)

Target

See all ACSL4 Antibodies
ACSL4 (Acyl-CoA Synthetase Long-Chain Family Member 4 (ACSL4))

Reactivity

  • 71
  • 26
  • 24
  • 4
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 70
  • 3
  • 1
Rabbit

Clonality

  • 65
  • 9
Polyclonal

Conjugate

  • 40
  • 5
  • 4
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This ACSL4 antibody is un-conjugated

Application

  • 63
  • 27
  • 26
  • 22
  • 17
  • 11
  • 9
  • 5
  • 1
Western Blotting (WB), ELISA
  • Binding Specificity

    • 10
    • 7
    • 7
    • 6
    • 6
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 28-56

    Cross-Reactivity (Details)

    Expected species reactivity: Mouse,Rat

    Purification

    Antigen affinity purified

    Immunogen

    A portion of amino acids 28-56 from the human protein was used as the immunogen for this FACL4 antibody.

    Isotype

    Ig Fraction
  • Application Notes

    Western blot: 1:500-1:1000

    Restrictions

    For Research Use only
  • Buffer

    In 1X PBS, pH 7.4, with 0.09 % sodium azide

    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

    Aliquot the FACL4 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • Target

    ACSL4 (Acyl-CoA Synthetase Long-Chain Family Member 4 (ACSL4))

    Alternative Name

    ACSL4 / FACL4

    Background

    The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme preferentially utilizes arachidonate as substrate. The absence of this enzyme may contribute to the mental retardation or Alport syndrome. Alternative splicing of this gene generates 2 transcript variants.

    UniProt

    O60488
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