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POC1A Protein (Myc-DYKDDDDK Tag)

POC1A Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2735520
  • Antigène Voir toutes POC1A Protéines
    POC1A (POC1 Centriolar Protein Homolog A (POC1A))
    Type de proteíne
    Recombinant
    Origine
    • 2
    • 1
    • 1
    • 1
    Humain
    Source
    • 2
    • 2
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette POC1A protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human WDR51A 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 POC1A 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
    POC1A (POC1 Centriolar Protein Homolog A (POC1A))
    Autre désignation
    Wdr51a (POC1A Produits)
    Synonymes
    PIX2 Protein, SOFT Protein, WDR51A Protein, 2510040D07Rik Protein, Wdr51a Protein, RGD1565004 Protein, wdr51a Protein, wu:fl82d01 Protein, zgc:56055 Protein, POC1 centriolar protein A Protein, POC1A Protein, Poc1a Protein, poc1a Protein
    Sujet
    POC1 proteins contain an N-terminal WD40 domain and a C-terminal coiled coil domain and are part of centrosomes. They play an important role in basal body and cilia formation. This gene encodes one of the two POC1 proteins found in humans. Mutations in this gene result in short stature, onychodysplasia, facial dysmorphism, and hypotrichosis (SOFT) syndrome.
    Poids moléculaire
    44.8 kDa
    NCBI Accession
    NP_056241
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