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SUMF1 Protein (Myc-DYKDDDDK Tag)

SUMF1 Spezies: Human Wirt: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Produktnummer ABIN2732973
  • Target Alle SUMF1 Proteine anzeigen
    SUMF1 (Sulfatase Modifying Factor 1 (SUMF1))
    Protein-Typ
    Recombinant
    Spezies
    • 8
    • 1
    • 1
    Human
    Quelle
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    HEK-293 Cells
    Aufreinigungstag / Konjugat
    Dieses SUMF1 Protein ist gelabelt mit Myc-DYKDDDDK Tag.
    Applikation
    Antibody Production (AbP), Standard (STD)
    Produktmerkmale
    • Recombinant human SUMF1 / FGE 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 SUMF1 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
    SUMF1 (Sulfatase Modifying Factor 1 (SUMF1))
    Andere Bezeichnung
    Sumf1,fge (SUMF1 Produkte)
    Synonyme
    AAPA3037 Protein, FGE Protein, AA543204 Protein, AI463102 Protein, AI851573 Protein, sulfatase modifying factor 1 Protein, SUMF1 Protein, Sumf1 Protein
    Hintergrund
    This gene encodes an enzyme that catalyzes the hydrolysis of sulfate esters by oxidizing a cysteine residue in the substrate sulfatase to an active site 3-oxoalanine residue, which is also known as C-alpha-formylglycine. Mutations in this gene cause multiple sulfatase deficiency, a lysosomal storage disorder. Alternative splicing results in multiple transcript variants.
    Molekulargewicht
    37.3 kDa
    NCBI Accession
    NP_877437
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