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ACADL anticorps (AA 14-43)

Cet anticorps Lapin Polyclonal détecte spécifiquement ACADL dans WB et ELISA. Il présente une réactivité envers Humain, Souris et Rat.
N° du produit ABIN5647677

Aperçu rapide pour ACADL anticorps (AA 14-43) (ABIN5647677)

Antigène

Voir toutes ACADL Anticorps
ACADL (Acyl-CoA Dehydrogenase, Long Chain (ACADL))

Reactivité

  • 60
  • 26
  • 6
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 67
  • 1
Lapin

Clonalité

  • 68
Polyclonal

Conjugué

  • 26
  • 6
  • 5
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
Cet anticorp ACADL est non-conjugé

Application

  • 49
  • 30
  • 26
  • 26
  • 12
  • 8
  • 6
  • 5
  • 4
Western Blotting (WB), ELISA
  • Épitope

    • 15
    • 15
    • 8
    • 7
    • 6
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 14-43

    Purification

    Antigen affinity purified

    Immunogène

    A portion of amino acids 14-43 from the human protein was used as the immunogen for this ACADL antibody.

    Isotype

    Ig Fraction
  • Indications d'application

    Western blot: 1:500-1000

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

    ACADL (Acyl-CoA Dehydrogenase, Long Chain (ACADL))

    Autre désignation

    ACADL

    Sujet

    Long-chain specific acyl-CoA dehydrogenase, mitochondrial belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia.

    UniProt

    P28330

    Pathways

    Monocarboxylic Acid Catabolic Process
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