Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

ACADL anticorps (N-Term)

ACADL Reactivité: Humain, Souris, Rat WB Hôte: Lapin Polyclonal RB32459 unconjugated
N° du produit ABIN657058
  • Antigène Voir toutes ACADL Anticorps
    ACADL (Acyl-CoA Dehydrogenase, Long Chain (ACADL))
    Épitope
    • 15
    • 15
    • 9
    • 8
    • 7
    • 6
    • 6
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 14-43, N-Term
    Reactivité
    • 58
    • 28
    • 5
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    Humain, Souris, Rat
    Hôte
    • 68
    • 1
    Lapin
    Clonalité
    • 69
    Polyclonal
    Conjugué
    • 22
    • 7
    • 6
    • 6
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    Cet anticorp ACADL est non-conjugé
    Application
    • 50
    • 35
    • 26
    • 26
    • 8
    • 8
    • 6
    • 2
    • 1
    Western Blotting (WB)
    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.
    Clone
    RB32459
    Isotype
    Ig Fraction
    Top Product
    Discover our top product ACADL Anticorps primaire
  • 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 (ACADL Produits)
    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
Vous êtes ici:
Support technique