Desmoplakin antibody (AA 69-2195)

Catalog No. ABIN7602296

This anti-Desmoplakin antibody is a Rabbit Polyclonal antibody detecting Desmoplakin in WB, ELISA and FACS. Suitable for Human.

Quick Overview for Desmoplakin antibody (AA 69-2195) (ABIN7602296)

Target: Desmoplakin (DSP)

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Desmoplakin antibody is un-conjugated

Application: Western Blotting (WB), ELISA, Flow Cytometry (FACS)

Product Details anti-Desmoplakin Antibody

Binding Specificity: AA 69-2195

Purpose: Anti-Desmoplakin/DSP Antibody

Cross-Reactivity (Details): No cross-reactivity with other proteins.

Characteristics: Anti-Desmoplakin/DSP Antibody (ABIN7602296). Tested in ELISA, Flow Cytometry, WB applications. This antibody reacts with Human. This is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.

Purification: Immunogen affinity purified.

Immunogen: E.coli-derived human Desmoplakin/DSP recombinant protein (Position: N69-H2195).

Isotype: IgG

Application Details

Application Notes: Western blot, 0.25-0.5 μg/mL, Human
Flow Cytometry (Fixed), 1-3 μg/1x10⁶ cells, Human
ELISA, 0.1-0.5 μg/mL, -

Restrictions: For Research Use only

Handling

Format: Lyophilized

Reconstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Concentration: 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Storage: 4 °C,-20 °C

Storage Comment: At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.

Target Details for Desmoplakin

Target: Desmoplakin (DSP)

Alternative Name: DSP

Background:

Synonyms: Desmoplakin, DP, 250/210 kDa paraneoplastic pemphigus antigen, DSP

Tissue Specificity: Isoform DPI is apparently an obligate constituent of all desmosomes. Isoform DPII resides predominantly in tissues and cells of stratified origin.

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.

Molecular Weight: 250 kDa

Gene ID: 1832

UniProt: P15924

Pathways: Cell-Cell Junction Organization