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DLL3 antibody (AA 62-286)

This Rabbit Polyclonal antibody specifically detects DLL3 in WB. It exhibits reactivity toward Human.
Catalog No. ABIN5027148

Quick Overview for DLL3 antibody (AA 62-286) (ABIN5027148)

Target

See all DLL3 Antibodies
DLL3 (delta Like Protein 3 (DLL3))

Reactivity

  • 63
  • 24
  • 7
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 57
  • 6
  • 3
Rabbit

Clonality

  • 56
  • 8
  • 1
Polyclonal

Conjugate

  • 29
  • 5
  • 5
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This DLL3 antibody is un-conjugated

Application

  • 48
  • 28
  • 22
  • 16
  • 13
  • 6
  • 4
  • 3
  • 2
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 7
    • 7
    • 6
    • 6
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 62-286

    Purification

    Protein A Chromatography

    Immunogen

    A partial length recombinant Delta like 3 protein (amino acids 62-286) was used as the immunogen for this antibody.

    Isotype

    IgG
  • Application Notes

    WB: 2-4 μg/mL

    Restrictions

    For Research Use only
  • Concentration

    0.5 mg/mL

    Buffer

    PBS containing 0.05 % BSA, PH 7.4

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store the antibody at 4°C, stable for 6 months. For long-term storage, store at -20°C. Avoid repeated freeze and thaw cycles.
  • Target

    DLL3 (delta Like Protein 3 (DLL3))

    Alternative Name

    Delta like 3

    Background

    Delta like 3 (DLL3) is a member of Delta/Serrate/Lag2 (DSL) ligands for Notch receptors and plays a role in Notch signaling. Out of Five DSL ligands, DLL3 is the most structurally divergent DSL ligand. DLL3 is expressed throughout the presomitic mesoderm and is localized to the rostral somatic compartments. Homozygous disruptions of Notch1 and DLL3 result in severe abnormalities in somitogenesis. Mutations in the human DLL3 homolog cause recessive skeletal abnormalities in spondylocostal dysostosis with a consistent pattern of abnormal segmentation.

    Molecular Weight

    65 kDa

    Gene ID

    10683

    UniProt

    Q9NYJ7

    Pathways

    Notch Signaling
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