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ACSL4 anticorps (AA 36-237)

Cet anticorps anti-ACSL4 Polyclonal Lapin (ABIN7874305) détecte spécifiquement ACSL4 dans WB et ELISA. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.
N° du produit ABIN7874305
644,88 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour ACSL4 anticorps (AA 36-237) (ABIN7874305)

Antigène

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

Reactivité

  • 80
  • 35
  • 33
  • 4
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 78
  • 4
  • 1
Lapin

Clonalité

  • 64
  • 19
Polyclonal

Conjugué

  • 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
Cet anticorp ACSL4 est non-conjugé

Application

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

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

    Fonction

    FACL4 Antibody / ACSL4

    Purification

    Antigen affinity purified

    Immunogène

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

    Isotype

    IgG
  • Indications d'application

    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

    Stock

    4 °C,-20 °C

    Stockage commentaire

    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.
  • Antigène

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

    Autre désignation

    FACL4

    Sujet

    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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