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ETHE1 Protein (Myc-DYKDDDDK Tag)

ETHE1 Spezies: Human Wirt: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Produktnummer ABIN2720574
  • Target Alle ETHE1 Proteine anzeigen
    ETHE1 (Ethylmalonic Encephalopathy 1 (ETHE1))
    Protein-Typ
    Recombinant
    Spezies
    • 5
    • 1
    • 1
    Human
    Quelle
    • 2
    • 2
    • 2
    • 1
    HEK-293 Cells
    Aufreinigungstag / Konjugat
    Dieses ETHE1 Protein ist gelabelt mit Myc-DYKDDDDK Tag.
    Applikation
    Antibody Production (AbP), Standard (STD)
    Produktmerkmale
    • Recombinant human ETHE1 / HSCO 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 ETHE1 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
    ETHE1 (Ethylmalonic Encephalopathy 1 (ETHE1))
    Andere Bezeichnung
    Ethe1,hsco (ETHE1 Produkte)
    Synonyme
    zgc:85680 Protein, HSCO Protein, YF13H12 Protein, 0610025L15Rik Protein, Hsco Protein, ETHE1, persulfide dioxygenase Protein, ethylmalonic encephalopathy 1 Protein, Ethe1 Protein, ethe1 Protein, ETHE1 Protein
    Hintergrund
    This gene encodes a member of the metallo beta-lactamase family of iron-containing proteins involved in the mitochondrial sulfide oxidation pathway. The encoded protein catalyzes the oxidation of a persulfide substrate to sulfite. Certain mutations in this gene cause ethylmalonic encephalopathy, an infantile metabolic disorder affecting the brain, gastrointestinal tract and peripheral vessels. Alternative splicing results in multiple transcript variants encoding different isoforms.
    Molekulargewicht
    27.7 kDa
    NCBI Accession
    NP_055112
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