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

TCTN2 Spezies: Human Wirt: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Produktnummer ABIN2733404
  • Target Alle TCTN2 Proteine anzeigen
    TCTN2 (Tectonic Family Member 2 (TCTN2))
    Protein-Typ
    Recombinant
    Proteineigenschaft
    Transcript Variant 1
    Spezies
    • 2
    • 2
    • 1
    Human
    Quelle
    • 4
    • 1
    HEK-293 Cells
    Aufreinigungstag / Konjugat
    Dieses TCTN2 Protein ist gelabelt mit Myc-DYKDDDDK Tag.
    Applikation
    Antibody Production (AbP), Standard (STD)
    Produktmerkmale
    • Recombinant human Tectonic-2 (transcript variant 1) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Reinheit
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product TCTN2 Protein
  • Applikationshinweise
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Kommentare

    The tag is located at the C-terminal.

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Konzentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    Lagerung
    -80 °C
    Informationen zur Lagerung
    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.
  • Target
    TCTN2 (Tectonic Family Member 2 (TCTN2))
    Andere Bezeichnung
    Tectonic-2 (TCTN2 Produkte)
    Synonyme
    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
    Hintergrund
    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.
    Molekulargewicht
    76.7 kDa
    NCBI Accession
    NP_079085
    Pathways
    Proton Transport
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