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ACADL anticorps (N-Term)

Cet anticorps Lapin Polyclonal détecte spécifiquement ACADL dans WB. Il présente une réactivité envers Humain, Souris et Rat.
N° du produit ABIN657058

Aperçu rapide pour ACADL anticorps (N-Term) (ABIN657058)

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
  • 31
  • 26
  • 26
  • 12
  • 8
  • 6
  • 5
  • 4
Western Blotting (WB)

Clone

RB32459
  • Épitope

    • 15
    • 15
    • 8
    • 7
    • 6
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 14-43, N-Term

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogène

    This ACADL antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 14-43 amino acids from the N-terminal region of human ACADL.

    Isotype

    Ig Fraction
  • Indications d'application

    WB: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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

    Date de péremption

    6 months
  • Antigène

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

    Autre désignation

    ACADL

    Sujet

    The protein encoded by this gene 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.

    Poids moléculaire

    47656

    NCBI Accession

    NP_001599

    UniProt

    P28330

    Pathways

    Monocarboxylic Acid Catabolic Process
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