ACSL4 anticorps (AA 28-56)

N° du produit ABIN7479739

Cet anticorps Lapin Polyclonal détecte spécifiquement ACSL4 dans WB et ELISA. Il présente une réactivité avec des échantillons de Humain.

Aperçu rapide pour ACSL4 anticorps (AA 28-56) (ABIN7479739)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ACSL4 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-ACSL4 anticorps

Épitope: AA 28-56

Fonction: FACL4 Antibody / ACSL4

Réactivité croisée (Details): Expected species reactivity: Mouse,Rat

Purification: Antigen affinity

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

Isotype: Ig Fraction

Information d'application

Indications d'application: Titration of the FACL4 antibody may be required due to differences in protocols and secondary/substrate sensitivity.

Restrictions: For Research Use only

Stockage

Format: Liquid

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: 4 °C,-20 °C

Stockage commentaire: Aliquot the FACL4 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

Détails sur ACSL4

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

Autre désignation: 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