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Oligophrenin 1 Protein (OPHN1) (Myc-DYKDDDDK Tag)

OPHN1 Spezies: Human Wirt: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Produktnummer ABIN2727904
  • Target Alle Oligophrenin 1 (OPHN1) Proteine anzeigen
    Oligophrenin 1 (OPHN1)
    Protein-Typ
    Recombinant
    Spezies
    • 3
    • 2
    • 1
    Human
    Quelle
    • 2
    • 2
    • 2
    HEK-293 Cells
    Aufreinigungstag / Konjugat
    Dieses Oligophrenin 1 Protein ist gelabelt mit Myc-DYKDDDDK Tag.
    Applikation
    Antibody Production (AbP), Standard (STD)
    Produktmerkmale
    • Recombinant human Oligophrenin-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 OPHN1 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
    Oligophrenin 1 (OPHN1)
    Andere Bezeichnung
    Oligophrenin-1 (OPHN1 Produkte)
    Synonyme
    ARHGAP41 Protein, MRX60 Protein, OPN1 Protein, C130037N19Rik Protein, Opn1 Protein, MGC68856 Protein, zgc:92603 Protein, OPHN1 Protein, mrx60 Protein, opn1 Protein, oligophrenin 1 Protein, oligophrenin 1 L homeolog Protein, OPHN1 Protein, Ophn1 Protein, ophn1.L Protein, ophn1 Protein, Tsp_13482 Protein
    Hintergrund
    This gene encodes a Rho-GTPase-activating protein that promotes GTP hydrolysis of Rho subfamily members. Rho proteins are important mediators of intracellular signal transduction, which affects cell migration and cell morphogenesis. Mutations in this gene are responsible for OPHN1-related X-linked mental retardation with cerebellar hypoplasia and distinctive facial dysmorhphism.
    Molekulargewicht
    91.5 kDa
    NCBI Accession
    NP_002538
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