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Peroxidasin Protein (Myc-DYKDDDDK Tag)

PXDN Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2730195
  • Antigène Voir toutes Peroxidasin (PXDN) Protéines
    Peroxidasin (PXDN) (Peroxidasin Homolog (PXDN))
    Type de proteíne
    Recombinant
    Origine
    • 5
    • 1
    Humain
    Source
    • 3
    • 2
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette Peroxidasin protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human PXDN 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 PXDN 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
    Peroxidasin (PXDN) (Peroxidasin Homolog (PXDN))
    Autre désignation
    Pxdn (PXDN Produits)
    Synonymes
    D2S448 Protein, D2S448E Protein, MG50 Protein, PRG2 Protein, PXN Protein, VPO Protein, 2310075M15Rik Protein, C85409 Protein, E330004E07 Protein, VPO1 Protein, mKIAA0230 Protein, peroxidasin Protein, PXDN Protein, Pxdn Protein
    Sujet
    This gene encodes a heme-containing peroxidase that is secreted into the extracellular matrix. It is involved in extracellular matrix formation, and may function in the physiological and pathological fibrogenic response in fibrotic kidney. Mutations in this gene cause corneal opacification and other ocular anomalies, and also microphthalmia and anterior segment dysgenesis.
    Poids moléculaire
    165.1 kDa
    NCBI Accession
    NP_036425
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