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TCTN2 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

TCTN2 Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2733404
  • Antigène Voir toutes TCTN2 Protéines
    TCTN2 (Tectonic Family Member 2 (TCTN2))
    Type de proteíne
    Recombinant
    Attributs du protein
    Transcript Variant 1
    Origine
    • 2
    • 2
    • 1
    Humain
    Source
    • 4
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette TCTN2 protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human Tectonic-2 (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 TCTN2 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
    TCTN2 (Tectonic Family Member 2 (TCTN2))
    Autre désignation
    Tectonic-2 (TCTN2 Produits)
    Synonymes
    fb44f11 Protein, wu:fb44f11 Protein, tect2 Protein, C12orf38 Protein, MKS8 Protein, TECT2 Protein, 4432405B04Rik Protein, Tect2 Protein, tectonic family member 2 Protein, TCTN2 Protein, tctn2 Protein, Tctn2 Protein
    Sujet
    This gene encodes a type I membrane protein that belongs to the tectonic family. Studies in mice suggest that this protein may be involved in hedgehog signaling, and essential for ciliogenesis. Mutations in this gene are associated with Meckel syndrome type 8. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
    Poids moléculaire
    76.7 kDa
    NCBI Accession
    NP_079085
    Pathways
    Proton Transport
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