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LEPRE1 Protein (Myc-DYKDDDDK Tag)

LEPRE1 Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2724652
  • Antigène Voir toutes LEPRE1 Protéines
    LEPRE1 (Leucine Proline-Enriched Proteoglycan (Leprecan) 1 (LEPRE1))
    Type de proteíne
    Recombinant
    Origine
    • 3
    • 1
    • 1
    Humain
    Source
    • 2
    • 2
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette LEPRE1 protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human LEPRE1 protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Pureté
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product LEPRE1 Protéine
  • Indications d'application
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Commentaires

    The tag is located at the C-terminal.

    Restrictions
    For Research Use only
  • Concentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    Stock
    -80 °C
    Stockage commentaire
    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.
  • Antigène
    LEPRE1 (Leucine Proline-Enriched Proteoglycan (Leprecan) 1 (LEPRE1))
    Autre désignation
    Lepre1 (LEPRE1 Produits)
    Synonymes
    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
    Sujet
    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.
    Poids moléculaire
    83.2 kDa
    NCBI Accession
    NP_071751
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