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FLCN Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

FLCN Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2721298
  • Antigène Voir toutes FLCN Protéines
    FLCN (Folliculin (FLCN))
    Type de proteíne
    Recombinant
    Attributs du protein
    Transcript Variant 1
    Origine
    • 5
    • 1
    • 1
    Humain
    Source
    • 2
    • 2
    • 2
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette FLCN protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human Folliculin (transcript variant 1) 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 FLCN 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
    FLCN (Folliculin (FLCN))
    Autre désignation
    Folliculin (FLCN Produits)
    Synonymes
    FLCN Protein, flcn Protein, wu:fe38g11 Protein, zgc:136982 Protein, AU014660 Protein, B430214A04Rik Protein, Bhd Protein, FLCL Protein, BHD Protein, folliculin Protein, folliculin S homeolog Protein, FLCN Protein, flcn Protein, flcn.S Protein, Flcn Protein
    Classe de substances
    Amino Acid
    Sujet
    This gene is located within the Smith-Magenis syndrome region on chromosome 17. Mutations in this gene are associated with Birt-Hogg-Dube syndrome, which is characterized by fibrofolliculomas, renal tumors, lung cysts, and pneumothorax. Alternative splicing of this gene results in two transcript variants encoding different isoforms.
    Poids moléculaire
    64.3 kDa
    NCBI Accession
    NP_659434
    Pathways
    Cell-Cell Junction Organization
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