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SOX14 Protein (Myc-DYKDDDDK Tag)

SOX14 Spezies: Human Wirt: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Produktnummer ABIN2732432
  • Target Alle SOX14 Proteine anzeigen
    SOX14 (SRY (Sex Determining Region Y)-Box 14 (SOX14))
    Protein-Typ
    Recombinant
    Spezies
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Quelle
    • 5
    • 2
    HEK-293 Cells
    Aufreinigungstag / Konjugat
    Dieses SOX14 Protein ist gelabelt mit Myc-DYKDDDDK Tag.
    Applikation
    Antibody Production (AbP), Standard (STD)
    Produktmerkmale
    • Recombinant human SOX14 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 SOX14 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
    SOX14 (SRY (Sex Determining Region Y)-Box 14 (SOX14))
    Andere Bezeichnung
    Sox14 (SOX14 Produkte)
    Synonyme
    SOX28 Protein, zgc:123197 Protein, SRY-box 14 Protein, SRY-box 14 S homeolog Protein, SRY box 14 Protein, SRY (sex determining region Y)-box 14 Protein, SOX14 Protein, sox14.S Protein, Sox14 Protein, sox14 Protein
    Hintergrund
    This intronless gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. Mutations in this gene are suggested to be responsible for the limb defects associated with blepharophimosis, ptosis, epicanthus inversus syndrome (BPES) and Mobius syndrome.
    Molekulargewicht
    26.3 kDa
    NCBI Accession
    NP_004180
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