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CLN5 Protein (Myc-DYKDDDDK Tag)

CLN5 Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2713927
  • Antigène Voir toutes CLN5 Protéines
    CLN5 (Ceroid-Lipofuscinosis, Neuronal 5 (CLN5))
    Type de proteíne
    Recombinant
    Origine
    • 1
    • 1
    • 1
    • 1
    Humain
    Source
    • 3
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette CLN5 protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human CLN5 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 CLN5 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
    CLN5 (Ceroid-Lipofuscinosis, Neuronal 5 (CLN5))
    Abstract
    CLN5 Produits
    Synonymes
    NCL Protein, A730075N08Rik Protein, CLN5, intracellular trafficking protein Protein, ceroid-lipofuscinosis, neuronal 5 Protein, CLN5 Protein, Cln5 Protein
    Sujet
    This gene is one of eight which have been associated with neuronal ceroid lipofuscinoses (NCL). Also referred to as Batten disease, NCL comprises a class of autosomal recessive, neurodegenerative disorders affecting children. The genes responsible likely encode proteins involved in the degradation of post-translationally modified proteins in lysosomes. The primary defect in NCL disorders is thought to be associated with lysosomal storage function.[provided by RefSeq, Oct 2008].
    Poids moléculaire
    46.2 kDa
    NCBI Accession
    NP_006484
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