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ACSL4 antibody (AA 36-237)

The Rabbit Polyclonal anti-ACSL4 antibody (ABIN7874305) specifically detects ACSL4 in WB and ELISA. The antibody is reactive with Human, Mouse and Rat samples.
Catalog No. ABIN7874305
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for ACSL4 antibody (AA 36-237) (ABIN7874305)

Target

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

Reactivity

  • 80
  • 35
  • 33
  • 4
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 78
  • 4
  • 1
Rabbit

Clonality

  • 64
  • 19
Polyclonal

Conjugate

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

Application

  • 72
  • 34
  • 32
  • 27
  • 25
  • 10
  • 9
  • 7
  • 1
  • 1
Western Blotting (WB), ELISA
  • Binding Specificity

    • 10
    • 8
    • 7
    • 6
    • 5
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 36-237

    Purpose

    FACL4 Antibody / ACSL4

    Purification

    Antigen affinity purified

    Immunogen

    Recombinant human FACL4/ACSL4 protein (amino acids A36-E237) was used as the immunogen for the FACL4 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the FACL4 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the FACL4 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

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

    Alternative Name

    FACL4

    Background

    Long-chain-fatty-acid--CoA ligase 4 is an enzyme that in humans is encoded by the ACSL4 gene. It is mapped to Xq23. 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 cognitive disability or Alport syndrome. Alternative splicing of this gene generates multiple transcript variants.

    UniProt

    O60488
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