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DLL3 antibody (AA 400-618)

The Mouse Monoclonal anti-DLL3 antibody is suitable to detect DLL3 in samples from Human. It has been validated for IHC (p).
Catalog No. ABIN7874781
$640.46
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for DLL3 antibody (AA 400-618) (ABIN7874781)

Target

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

Reactivity

  • 84
  • 35
  • 20
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 58
  • 19
  • 10
  • 1
Mouse

Clonality

  • 55
  • 29
  • 2
Monoclonal

Conjugate

  • 38
  • 8
  • 6
  • 5
  • 5
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This DLL3 antibody is un-conjugated

Application

  • 49
  • 28
  • 21
  • 18
  • 11
  • 8
  • 5
  • 1
  • 1
  • 1
Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Grade

Carrier-free

Clone

DLL3-9361
  • Binding Specificity

    • 8
    • 7
    • 7
    • 5
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 400-618

    Purpose

    DLL3 Antibody / Delta-like protein 3 (azide and preservative free)

    Purification

    Protein A/G affinity

    Immunogen

    A portion of amino acids 400-618 from human DLL3 protein was used as the immunogen for the DLL3 antibody.

    Isotype

    IgG2c, kappa
  • Application Notes

    Optimal dilution of the DLL3 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    1 mg/mL in 1X PBS, BSA free, sodium azide free

    Preservative

    Azide free

    Storage

    -20 °C

    Storage Comment

    Aliquot the DLL3 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
  • Target

    DLL3 (delta Like Protein 3 (DLL3))

    Alternative Name

    DLL3

    Background

    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.

    UniProt

    Q9NYJ7

    Pathways

    Notch Signaling
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