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FKBP1A Protein (Transcript Variant 12A) (Myc-DYKDDDDK Tag)

FKBP1A Spezies: Human Wirt: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Produktnummer ABIN2721206
  • Target Alle FKBP1A Proteine anzeigen
    FKBP1A (FK506 Binding Protein 1A, 12kDa (FKBP1A))
    Protein-Typ
    Recombinant
    Proteineigenschaft
    Transcript Variant 12A
    Spezies
    • 10
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human
    Quelle
    • 11
    • 5
    • 1
    • 1
    HEK-293 Cells
    Aufreinigungstag / Konjugat
    Dieses FKBP1A Protein ist gelabelt mit Myc-DYKDDDDK Tag.
    Applikation
    Antibody Production (AbP), Standard (STD)
    Produktmerkmale
    • Recombinant human FKBP1A / FKBP12 (transcript variant 12A) 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 FKBP1A 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
    FKBP1A (FK506 Binding Protein 1A, 12kDa (FKBP1A))
    Andere Bezeichnung
    Fkbp1a,fkbp12 (FKBP1A Produkte)
    Hintergrund
    The protein encoded by this gene is a member of the immunophilin protein family, which play a role in immunoregulation and basic cellular processes involving protein folding and trafficking. The protein is a cis-trans prolyl isomerase that binds the immunosuppressants FK506 and rapamycin. It interacts with several intracellular signal transduction proteins including type I TGF-beta receptor. It also interacts with multiple intracellular calcium release channels, and coordinates multi-protein complex formation of the tetrameric skeletal muscle ryanodine receptor. In mouse, deletion of this homologous gene causes congenital heart disorder known as noncompaction of left ventricular myocardium. Multiple alternatively spliced variants, encoding the same protein, have been identified. The human genome contains five pseudogenes related to this gene, at least one of which is transcribed.
    Molekulargewicht
    11.8 kDa
    NCBI Accession
    NP_463460
    Pathways
    Negative Regulation of Transporter Activity, Methionine Biosynthetic Process
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