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delta Like Protein 3 (DLL3) (N-Term) Peptid

DLL3 Reaktivität: Human Wirt: Synthetic BP, WB
Produktnummer ABIN975832
  • Target Alle DLL3 Produkte
    DLL3 (delta Like Protein 3 (DLL3))
    Protein Region
    N-Term
    Spezies
    Human
    Quelle
    • 2
    Synthetic
    Applikation
    Blocking Peptide (BP), Western Blotting (WB)
    Produktmerkmale
    This is a synthetic peptide designed for use in combination with anti-DLL3 antibody (Catalog #: ARP47292_P050). 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.
    Aufreinigung
    Purified
  • Applikationshinweise
    Each Investigator should determine their own optimal working dilution for specific applications.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Rekonstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Konzentration
    1 mg/mL
    Buffer
    Final peptide concentration is 1 mg/mL in PBS.
    Handhabung
    Avoid repeated freeze-thaw cycles.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target
    DLL3 (delta Like Protein 3 (DLL3))
    Synonyme
    SCDO1 Peptide, pu Peptide, pudgy Peptide, delta like canonical Notch ligand 3 Peptide, delta-like 3 (Drosophila) Peptide, DLL3 Peptide, Dll3 Peptide
    Hintergrund
    DLL3 is a member of the delta protein ligand family. This family functions as Notch ligands that are characterized by a DSL domain, EGF repeats, and a transmembrane domain. Mutations in this gene cause autosomal recessive spondylocostal dysostosis 1. Two transcript variants encoding distinct isoforms have been identified for this gene. This gene encodes a member of the delta protein ligand family. This family functions as Notch ligands that are characterized by a DSL domain, EGF repeats, and a transmembrane domain. Mutations in this gene cause autosomal recessive spondylocostal dysostosis 1. Two transcript variants encoding distinct isoforms have been identified for this gene.

    Alias Symbols: SCDO1

    Protein Size: 618
    Molekulargewicht
    54 kDa
    Gen-ID
    10683
    NCBI Accession
    NM_016941, NP_058637
    UniProt
    Q9NYJ7
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