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ACSL4 anticorps (AA 28-56)

Cet anticorps Lapin Polyclonal détecte spécifiquement ACSL4 dans WB et ELISA. Il présente une réactivité envers Humain.
N° du produit ABIN5647455

Aperçu rapide pour ACSL4 anticorps (AA 28-56) (ABIN5647455)

Antigène

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

Reactivité

  • 69
  • 26
  • 24
  • 4
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 68
  • 3
  • 1
Lapin

Clonalité

  • 63
  • 9
Polyclonal

Conjugué

  • 38
  • 5
  • 4
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp ACSL4 est non-conjugé

Application

  • 61
  • 26
  • 24
  • 22
  • 16
  • 10
  • 9
  • 5
  • 1
Western Blotting (WB), ELISA
  • Épitope

    • 10
    • 7
    • 7
    • 6
    • 5
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 28-56

    Réactivité croisée (Details)

    Expected species reactivity: Mouse,Rat

    Purification

    Antigen affinity purified

    Immunogène

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

    Isotype

    Ig Fraction
  • Indications d'application

    Western blot: 1:500-1:1000

    Restrictions

    For Research Use only
  • Buffer

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

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    -20 °C

    Stockage commentaire

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

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

    Autre désignation

    ACSL4 / FACL4

    Sujet

    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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