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IBA57 Protein (Myc-DYKDDDDK Tag)

IBA57 Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2714026
  • Antigène Voir toutes IBA57 Protéines
    IBA57 (IBA57, Iron-Sulfur Cluster Assembly Homolog (IBA57))
    Type de proteíne
    Recombinant
    Origine
    • 1
    • 1
    • 1
    Humain
    Source
    • 1
    • 1
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette IBA57 protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human IBA57 protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Pureté
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product IBA57 Protéine
  • Indications d'application
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Commentaires

    The tag is located at the C-terminal.

    Restrictions
    For Research Use only
  • Concentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    Stock
    -80 °C
    Stockage commentaire
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Antigène
    IBA57 (IBA57, Iron-Sulfur Cluster Assembly Homolog (IBA57))
    Autre désignation
    Chromosome 1 Open Reading Frame 69 (c1orf69) (IBA57 Produits)
    Synonymes
    C1orf69 Protein, 4930543L23Rik Protein, A230051G13Rik Protein, zgc:153540 Protein, IBA57 homolog, iron-sulfur cluster assembly Protein, IBA57 Protein, Iba57 Protein, iba57 Protein
    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.
    Poids moléculaire
    38 kDa
    NCBI Accession
    NP_001010867
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