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IBA57 antibody

IBA57 Reactivity: Human ELISA, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7248347
  • Target See all IBA57 Antibodies
    IBA57 (IBA57, Iron-Sulfur Cluster Assembly Homolog (IBA57))
    Reactivity
    • 16
    • 11
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 26
    Rabbit
    Clonality
    • 26
    Polyclonal
    Conjugate
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    This IBA57 antibody is un-conjugated
    Application
    • 17
    • 13
    • 13
    • 6
    • 3
    • 3
    • 1
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogen
    Synthetic peptide of human IBA57
    Isotype
    IgG
    Top Product
    Discover our top product IBA57 Primary Antibody
  • Application Notes
    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
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    IBA57 (IBA57, Iron-Sulfur Cluster Assembly Homolog (IBA57))
    Alternative Name
    IBA57 (IBA57 Products)
    Synonyms
    C1orf69 antibody, 4930543L23Rik antibody, A230051G13Rik antibody, zgc:153540 antibody, IBA57 homolog, iron-sulfur cluster assembly antibody, IBA57 antibody, Iba57 antibody, iba57 antibody
    Background
    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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