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CEP41 Protein (Myc-DYKDDDDK Tag)

CEP41 Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2734444
  • Antigène Voir toutes CEP41 Protéines
    CEP41 (Centrosomal Protein 41kDa (CEP41))
    Type de proteíne
    Recombinant
    Origine
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain
    Source
    • 5
    • 1
    • 1
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette CEP41 protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human TSGA14 / CEP41 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 CEP41 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
    CEP41 (Centrosomal Protein 41kDa (CEP41))
    Autre désignation
    Tsga14,cep41 (CEP41 Produits)
    Synonymes
    1700017E11Rik Protein, 2810431D15Rik Protein, AI449046 Protein, AI503610 Protein, Tsga14 Protein, JBTS15 Protein, TSGA14 Protein, Cep41-A Protein, tsga14 Protein, RPL37A Protein, centrosomal protein 41 Protein, centrosomal protein 41kDa S homeolog Protein, Cep41 Protein, CEP41 Protein, cep41.S Protein
    Sujet
    This gene encodes a centrosomal and microtubule-binding protein which is predicted to have two coiled-coil domains and a rhodanese domain. In human retinal pigment epithelial cells the protein localized to centrioles and cilia. Mutations in this gene have been associated with Joubert Syndrome 15 an autosomal recessive ciliopathy and neurological disorder. Alternative splicing results in multiple transcript variants.
    Poids moléculaire
    41.2 kDa
    NCBI Accession
    NP_061188
    Pathways
    M Phase
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