Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

Desmoplakin antibody (AA 69-2195)

The Rabbit Polyclonal anti-Desmoplakin antibody is suitable to detect Desmoplakin in samples from Human. It has been validated for WB, ELISA and FACS.
Catalog No. ABIN7876440
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for Desmoplakin antibody (AA 69-2195) (ABIN7876440)

Target

See all Desmoplakin (DSP) Antibodies
Desmoplakin (DSP)

Reactivity

  • 46
  • 15
  • 15
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 40
  • 4
  • 2
  • 1
Rabbit

Clonality

  • 32
  • 15
Polyclonal

Conjugate

  • 27
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
This Desmoplakin antibody is un-conjugated

Application

  • 28
  • 15
  • 15
  • 12
  • 12
  • 6
  • 4
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • Binding Specificity

    • 5
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 69-2195

    Purpose

    DSP Antibody / Desmoplakin

    Purification

    Antigen affinity purified

    Immunogen

    Recombinant human protein (amino acids N69-H2195) was used as the immunogen for the DSP antibody.

    Isotype

    IgG
  • Application Notes

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

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the DSP antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    Desmoplakin (DSP)

    Alternative Name

    DSP

    Background

    Desmoplakin is a protein in humans that is encoded by the DSP gene. This gene encodes a protein that anchors intermediate filaments to desmosomal plaques and forms an obligate component of functional desmosomes. Mutations in this gene are the cause of several cardiomyopathies and keratodermas, including skin fragility-woolly hair syndrome. Alternative splicing results in multiple transcript variants.

    UniProt

    P15924

    Pathways

    Cell-Cell Junction Organization
You are here:
Chat with us!