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DLL3 antibody

DLL3 Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN635694
  • Target See all DLL3 Antibodies
    DLL3 (delta Like Protein 3 (DLL3))
    Reactivity
    • 53
    • 24
    • 5
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    Human
    Host
    • 54
    • 2
    Rabbit
    Clonality
    • 54
    • 2
    Polyclonal
    Conjugate
    • 23
    • 6
    • 5
    • 5
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This DLL3 antibody is un-conjugated
    Application
    • 51
    • 27
    • 21
    • 19
    • 10
    • 3
    • 2
    • 2
    • 1
    Western Blotting (WB)
    Purification
    Affinity purified
    Immunogen
    DLL3 antibody was raised using a synthetic peptide corresponding to a region with amino acids MVSPRMSGLLSQTVILALIFLPQTRPAGVFELQIHSFGPGPGPGAPRSPC
    Top Product
    Discover our top product DLL3 Primary Antibody
  • Application Notes
    WB: 1 µg/mL
    Optimal conditions should be determined by the investigator.
    Comment

    DLL3 Blocking Peptide, catalog no. 33R-6609, is also available for use as a blocking control in assays to test for specificity of this DLL3 antibody

    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of DLL3 antibody in PBS
    Concentration
    Lot specific
    Buffer
    PBS
    Handling Advice
    Avoid repeated freeze/thaw cycles.
    Storage
    4 °C/-20 °C
    Storage Comment
    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • Target
    DLL3 (delta Like Protein 3 (DLL3))
    Alternative Name
    DLL3 (DLL3 Products)
    Synonyms
    SCDO1 antibody, pu antibody, pudgy antibody, delta like canonical Notch ligand 3 antibody, delta-like 3 (Drosophila) antibody, DLL3 antibody, Dll3 antibody
    Background
    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.
    Molecular Weight
    54 kDa (MW of target protein)
    Pathways
    Notch Signaling
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