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XPNPEP3 Protein (Myc-DYKDDDDK Tag)

XPNPEP3 Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2735673
  • Antigène Voir toutes XPNPEP3 Protéines
    XPNPEP3 (X-Prolyl Aminopeptidase (Aminopeptidase P) 3, Putative (XPNPEP3))
    Type de proteíne
    Recombinant
    Origine
    • 5
    • 1
    Humain
    Source
    • 3
    • 1
    • 1
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette XPNPEP3 protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human XPNPEP3 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 XPNPEP3 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
    XPNPEP3 (X-Prolyl Aminopeptidase (Aminopeptidase P) 3, Putative (XPNPEP3))
    Autre désignation
    Xpnpep3 (XPNPEP3 Produits)
    Synonymes
    APP3 Protein, NPHPL1 Protein, E430012M05Rik Protein, X-prolyl aminopeptidase 3 Protein, X-prolyl aminopeptidase 3, mitochondrial Protein, XPNPEP3 Protein, xpnpep3 Protein, Xpnpep3 Protein
    Sujet
    The protein encoded by this gene belongs to the family of X-pro-aminopeptidases that utilize a metal cofactor, and remove the N-terminal amino acid from peptides with a proline residue in the penultimate position. This protein has been shown to localize to the mitochondria of renal cells, and have a role in ciliary function. Mutations in this gene are associated with nephronophthisis-like nephropathy-1. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene, however, expression of some of these isoforms in vivo is not known.[provided by RefSeq, Mar 2011]
    Poids moléculaire
    56.9 kDa
    NCBI Accession
    NP_071381
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