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IDUA Protein (Myc-DYKDDDDK Tag)

IDUA Spezies: Human Wirt: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Produktnummer ABIN2723286
  • Target Alle IDUA Proteine anzeigen
    IDUA (Iduronidase, alpha-L- (IDUA))
    Protein-Typ
    Recombinant
    Spezies
    • 4
    • 1
    Human
    Quelle
    • 2
    • 2
    • 1
    HEK-293 Cells
    Aufreinigungstag / Konjugat
    Dieses IDUA Protein ist gelabelt mit Myc-DYKDDDDK Tag.
    Applikation
    Antibody Production (AbP), Standard (STD)
    Produktmerkmale
    • Recombinant human Alpha-L-iduronidase / IDUA 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 IDUA 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
    IDUA (Iduronidase, alpha-L- (IDUA))
    Andere Bezeichnung
    Iduronidase, alpha-L (Idua) (IDUA Produkte)
    Synonyme
    IDA Protein, MPS1 Protein, 6030426D08 Protein, alpha-L-iduronidase Protein, MGC80842 Protein, si:ch211-12e13.9 Protein, IDUA Protein, iduronidase, alpha-L- Protein, iduronidase, alpha-L- L homeolog Protein, alpha-L-iduronidase Protein, IDUA Protein, Idua Protein, idua.L Protein, idua Protein, LOC5564727 Protein
    Hintergrund
    This gene encodes an enzyme that hydrolyzes the terminal alpha-L-iduronic acid residues of two glycosaminoglycans, dermatan sulfate and heparan sulfate. This hydrolysis is required for the lysosomal degradation of these glycosaminoglycans. Mutations in this gene that result in enzymatic deficiency lead to the autosomal recessive disease mucopolysaccharidosis type I (MPS I).
    Molekulargewicht
    70 kDa
    NCBI Accession
    NP_000194
    Pathways
    Glycosaminoglycan Metabolic Process
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