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IBA57 Antikörper

IBA57 Reaktivität: Human ELISA, IHC Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7248347
  • Target Alle IBA57 Antikörper anzeigen
    IBA57 (IBA57, Iron-Sulfur Cluster Assembly Homolog (IBA57))
    Reaktivität
    • 16
    • 11
    • 1
    • 1
    • 1
    • 1
    Human
    Wirt
    • 26
    Kaninchen
    Klonalität
    • 26
    Polyklonal
    Konjugat
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser IBA57 Antikörper ist unkonjugiert
    Applikation
    • 17
    • 13
    • 13
    • 6
    • 3
    • 3
    • 1
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    Produktmerkmale
    Polyclonal Antibody
    Aufreinigung
    Antigen affinity purification
    Immunogen
    Synthetic peptide of human IBA57
    Isotyp
    IgG
    Top Product
    Discover our top product IBA57 Primärantikörper
  • Applikationshinweise
    IHC 1:30-1:150, ELISA 1:5000-1:10000
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    0.9 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    IBA57 (IBA57, Iron-Sulfur Cluster Assembly Homolog (IBA57))
    Andere Bezeichnung
    IBA57 (IBA57 Produkte)
    Synonyme
    C1orf69 antikoerper, 4930543L23Rik antikoerper, A230051G13Rik antikoerper, zgc:153540 antikoerper, IBA57 homolog, iron-sulfur cluster assembly antikoerper, IBA57 antikoerper, Iba57 antikoerper, iba57 antikoerper
    Hintergrund
    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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