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Peroxidasin Protein (Myc-DYKDDDDK Tag)

PXDN Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2730195
  • Target See all Peroxidasin (PXDN) Proteins
    Peroxidasin (PXDN) (Peroxidasin Homolog (PXDN))
    Protein Type
    Recombinant
    Origin
    • 5
    • 1
    Human
    Source
    • 3
    • 2
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This Peroxidasin protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human PXDN protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Purity
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product PXDN Protein
  • Application Notes
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Comment

    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.
    Storage
    -80 °C
    Storage Comment
    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
    Peroxidasin (PXDN) (Peroxidasin Homolog (PXDN))
    Alternative Name
    Pxdn (PXDN Products)
    Synonyms
    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
    Background
    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.
    Molecular Weight
    165.1 kDa
    NCBI Accession
    NP_036425
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