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Wilms Tumor 1 (WT1) (N-Term) Peptid

WT1 Reaktivität: Human Wirt: Synthetic WB, BP
Produktnummer ABIN5511631
  • Target Alle WT1 Produkte
    WT1 (Wilms Tumor 1 (WT1))
    Protein Region
    N-Term
    Spezies
    Human
    Quelle
    • 10
    Synthetic
    Applikation
    Western Blotting (WB), Blocking Peptide (BP)
    Sequenz
    DFAPPGASAY GSLGGPAPPP APPPPPPPPP HSFIKQEPSW GGAEPHEEQC
    Produktmerkmale
    This is a synthetic peptide designed for use in combination with anti-WT1 Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
  • Applikationshinweise
    Optimal working dilution should be determined by the investigator.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Rekonstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target
    WT1 (Wilms Tumor 1 (WT1))
    Synonyme
    AWT1 Peptide, EWS-WT1 Peptide, GUD Peptide, NPHS4 Peptide, WAGR Peptide, WIT-2 Peptide, WT33 Peptide, CWT1 Peptide, WT1 Peptide, XWT1a Peptide, wt-1 Peptide, wt1 Peptide, xWT1 Peptide, WT-1 Peptide, gud Peptide, wagr Peptide, wt33 Peptide, xwt1 Peptide, wit-2 Peptide, si:ch211-160j6.3 Peptide, zgc:152697 Peptide, D630046I19Rik Peptide, Wt-1 Peptide, XWT1b Peptide, XeWT1 Peptide, Wilms tumor 1 Peptide, Wilms tumor 1 S homeolog Peptide, wilms tumor 1b Peptide, Wilms tumor protein Peptide, Wilms tumor 1 homolog Peptide, Wilms tumor 1 L homeolog Peptide, WT1 Peptide, wt1.S Peptide, wt1 Peptide, wt1b Peptide, Wt1 Peptide, wt1.L Peptide
    Hintergrund
    WT1 is a transcription factor that contains four zinc-finger motifs at the C-terminus and a proline/glutamine-rich DNA-binding domain at the N-terminus. It has an essential role in the normal development of the urogenital system, and it is mutated in a small subset of patients with Wilm's tumors. Multiple transcript variants, resulting from alternative splicing at two coding exons, have been well characterized. There is also evidence for the use of non-AUG (CUG) translation initiation site upstream of, and in-frame with the first AUG, leading to additional isoforms.

    Protein Size: 432
    Gen-ID
    7490
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