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LEPRE1 Protein (Myc-DYKDDDDK Tag)

LEPRE1 Spezies: Human Wirt: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Produktnummer ABIN2724652
  • Target Alle LEPRE1 Proteine anzeigen
    LEPRE1 (Leucine Proline-Enriched Proteoglycan (Leprecan) 1 (LEPRE1))
    Protein-Typ
    Recombinant
    Spezies
    • 3
    • 1
    • 1
    Human
    Quelle
    • 2
    • 2
    • 1
    HEK-293 Cells
    Aufreinigungstag / Konjugat
    Dieses LEPRE1 Protein ist gelabelt mit Myc-DYKDDDDK Tag.
    Applikation
    Antibody Production (AbP), Standard (STD)
    Produktmerkmale
    • Recombinant human LEPRE1 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 LEPRE1 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
    LEPRE1 (Leucine Proline-Enriched Proteoglycan (Leprecan) 1 (LEPRE1))
    Andere Bezeichnung
    Lepre1 (LEPRE1 Produkte)
    Synonyme
    GROS1 Protein, OI8 Protein, P3H1 Protein, Gros1 Protein, MGC84556 Protein, LEPRE1 Protein, sb:cb953 Protein, 2410024C15Rik Protein, prolyl 3-hydroxylase 1 Protein, prolyl 3-hydroxylase 1 L homeolog Protein, P3H1 Protein, P3h1 Protein, p3h1.L Protein, p3h1 Protein
    Hintergrund
    This gene encodes an enzyme that is a member of the collagen prolyl hydroxylase family. These enzymes are localized to the endoplasmic reticulum and their activity is required for proper collagen synthesis and assembly. Mutations in this gene are associated with osteogenesis imperfecta type VIII. Three alternatively spliced transcript variants encoding different isoforms have been described. Other variants may exist, but their biological validity has not been determined.
    Molekulargewicht
    83.2 kDa
    NCBI Accession
    NP_071751
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