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IBA57 Protein (Myc-DYKDDDDK Tag)

IBA57 Spezies: Human Wirt: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Produktnummer ABIN2714026
  • Target Alle IBA57 Proteine anzeigen
    IBA57 (IBA57, Iron-Sulfur Cluster Assembly Homolog (IBA57))
    Protein-Typ
    Recombinant
    Spezies
    • 1
    • 1
    • 1
    Human
    Quelle
    • 1
    • 1
    • 1
    HEK-293 Cells
    Aufreinigungstag / Konjugat
    Dieses IBA57 Protein ist gelabelt mit Myc-DYKDDDDK Tag.
    Applikation
    Antibody Production (AbP), Standard (STD)
    Produktmerkmale
    • Recombinant human IBA57 protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Reinheit
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product IBA57 Protein
  • Applikationshinweise
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Kommentare

    The tag is located at the C-terminal.

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Konzentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    Lagerung
    -80 °C
    Informationen zur Lagerung
    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.
  • Target
    IBA57 (IBA57, Iron-Sulfur Cluster Assembly Homolog (IBA57))
    Andere Bezeichnung
    Chromosome 1 Open Reading Frame 69 (c1orf69) (IBA57 Produkte)
    Synonyme
    C1orf69 Protein, 4930543L23Rik Protein, A230051G13Rik Protein, zgc:153540 Protein, IBA57 homolog, iron-sulfur cluster assembly Protein, IBA57 Protein, Iba57 Protein, iba57 Protein
    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.
    Molekulargewicht
    38 kDa
    NCBI Accession
    NP_001010867
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