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IBA57 anticorps

IBA57 Reactivité: Humain ELISA, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7248347
  • Antigène Voir toutes IBA57 Anticorps
    IBA57 (IBA57, Iron-Sulfur Cluster Assembly Homolog (IBA57))
    Reactivité
    • 16
    • 11
    • 1
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 26
    Lapin
    Clonalité
    • 26
    Polyclonal
    Conjugué
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp IBA57 est non-conjugé
    Application
    • 17
    • 13
    • 13
    • 6
    • 3
    • 3
    • 1
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogène
    Synthetic peptide of human IBA57
    Isotype
    IgG
    Top Product
    Discover our top product IBA57 Anticorps primaire
  • Indications d'application
    IHC 1:30-1:150, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.9 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    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
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    IBA57 (IBA57, Iron-Sulfur Cluster Assembly Homolog (IBA57))
    Autre désignation
    IBA57 (IBA57 Produits)
    Synonymes
    anticorps C1orf69, anticorps 4930543L23Rik, anticorps A230051G13Rik, anticorps zgc:153540, anticorps IBA57 homolog, iron-sulfur cluster assembly, anticorps IBA57, anticorps Iba57, anticorps iba57
    Sujet
    The protein encoded by this gene localizes to the mitochondrion and is part of the iron-sulfur cluster assembly pathway. The encoded protein functions late in the biosynthesis of mitochondrial 4Fe-4S proteins. Defects in this gene have been associated with autosomal recessive spastic paraplegia-74 and with multiple mitochondrial dysfunctions syndrome-3. Two transcript variants encoding different isoforms have been found for this gene. The smaller isoform is not likely to be localized to the mitochondrion since it lacks the amino-terminal transit peptide.
    UniProt
    Q5T440
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