Millipore Sigma Vibrant Logo
Attention: We have moved. Merck Millipore products are no longer available for purchase on MerckMillipore.com.Learn More

CBL173 Anti-Desmoplakin 1& 2 Antibody, clone DP2.15

CBL173
50 µg  
Purchase on Sigma-Aldrich

Special Offers

Overview

Replacement Information

Key Spec Table

Species ReactivityKey ApplicationsHostFormatAntibody Type
B, Ch, H, M, RIF, WB, ICCMPurifiedMonoclonal Antibody
Description
Catalogue NumberCBL173
Brand Family Chemicon®
Trade Name
  • Chemicon
DescriptionAnti-Desmoplakin 1& 2 Antibody, clone DP2.15
References
Product Information
FormatPurified
HS Code3002 15 90
PresentationLyophilized. Reconstitute in 1 mL distilled water (final solution contains 0.09% sodium
azide, 0.5% BSA in PBS buffer, pH 7.4
Quality LevelMQ100
Applications
ApplicationAnti-Desmoplakin 1& 2 Antibody, clone DP2.15 detects level of Desmoplakin 1& 2 & has been published & validated for use in IF, WB & IC.
Key Applications
  • Immunofluorescence
  • Western Blotting
  • Immunocytochemistry
Application NotesWestern blot
Immunohistochemistry: 1:10; Frozen tissue
Immunofluorescence

Optimal working dilutions must be determined by the end user.
Biological Information
ImmunogenBovine desmoplakin 1 & 2
CloneDP2.15
HostMouse
SpecificityThis antibody shows distinct punctate membrane staining of desmoplakins 1 (MW 250 kDa) and 2 (MW 215 kDa) in stratified epithelia and simple epithelia, including glands, urothelium, thymic reticular epithelium, hepatocytes, intercalated disks of myocardium and arachnoid cells of meninges.
IsotypeIgG1
Species Reactivity
  • Bovine
  • Chicken
  • Human
  • Mouse
  • Rat
Antibody TypeMonoclonal Antibody
Entrez Gene Number
Entrez Gene SummaryDesmosomes are intercellular junctions that tightly link adjacent cells. Desmoplakin is an obligate component of functional desmosomes that anchors intermediate filaments to desmosomal plaques. The N-terminus of desmoplakin is required for localization to the desmosome and interacts with the N-terminal region of plakophilin 1 and plakoglobin. The C-terminus of desmoplakin binds with intermediate filaments. In the mid-region of desmoplakin, a coiled-coiled rod domain is responsible for homodimerization. Mutations in this gene are the cause of several cardiomyopathies and keratodermas as well as the autoimmune disease paraneoplastic pemphigus.
Gene Symbol
  • DSP
  • DPI
  • Desmoplakin
  • PPKS2
  • KPPS2
  • DP
  • DPII
UniProt Number
UniProt SummaryFUNCTION: SwissProt: P15924 # Major high molecular weight protein of desmosomes. Involved in the organization of the desmosomal cadherin- plakoglobin complexes into discrete plasma membrane domains and in the anchoring of intermediate filaments to the desmosomes.
SIZE: 2871 amino acids; 331774 Da
SUBUNIT: Homodimer.
SUBCELLULAR LOCATION: Note=Innermost portion of the desmosomal plaque.
TISSUE SPECIFICITY: Isoform DPI is apparently an obligate constituent of all desmosomes; Isoform DPII resides predominantly in tissues and cells of stratified origin.
DOMAIN: SwissProt: P15924 The N-terminal region is required for localization to the desmosomal plaque and interacts with the N-terminal region of plakophilin 1. The C-terminal region interacts with intermediate filaments.
PTM: Substrate of transglutaminase. Some glutamines and lysines are cross-linked to other desmoplakin molecules, to other proteins such as keratin, envoplakin, periplakin and involucrin, and to lipids like omega-hydroxyceramide.
DISEASE: "SwissProt: P15924 # Defects in DSP are the cause of keratosis palmoplantaris striata II (PPKS2) [MIM:125647]; also known as striate palmoplantar keratoderma II (SPPK2). PPKS2 is characterized by skin thickening in the palms (linear pattern) and the soles (island-like pattern) and flexor aspect of the fingers; and rarely by abnormalities of the nails, the teeth and the hair. & Defects in DSP are the cause of dilated cardiomyopathy with woolly hair and keratoderma (DCWHK) [MIM:605676]; also known as Carvajal syndrome or palmoplantar keratoderma with left ventricular cardiomyopathy and woolly hair. DCWHK is an autosomal recessive cardiocutaneous syndrome characterized by a generalized striate keratoderma particularly affecting the palmoplantar epidermis, woolly hair, and dilated left ventricular cardiomyopathy. & Defects in DSP are the cause of familial arrhythmogenic right ventricular dysplasia 8 (ARVD8) [MIM:607450]; also known as arrhythmogenic right ventricular cardiomyopathy 8 (ARVC8). ARVD is an autosomal dominant disease characterized by partial degeneration of the myocardium of the right ventricle, electrical instability, and sudden death. It is clinically defined by electrocardiographic and angiographic criteria; pathologic findings, replacement of ventricular myocardium with fatty and fibrous elements, preferentially involve the right ventricular free wall. & Defects in DSP are the cause of skin fragility-woolly hair syndrome (SFWHS) [MIM:607655]. SFWHS is an autosomal recessive genodermatosis characterized by focal and diffuse palmoplantar keratoderma, hyperkeratotic plaques on the trunk and limbs, and woolly hair with varying degrees of alopecia. & Defects in DSP are the cause of lethal acantholytic epidermolysis bullosa [MIM:609638]. Lethal acantholytic epidermolysis bullosa is characterized by severe fragility of skin and mucous membranes. The phenotype is lethal in the neonatal period because of immense transcutaneous fluid loss. Typical features include universal alopecia, neonatal teeth, and nail loss. Histopathology of the skin shows suprabasal clefting and acantholysis throughout the spinous layer, mimicking pemphigus."
SIMILARITY: Belongs to the plakin or cytolinker family. & Contains 17 plectin repeats. & Contains 2 spectrin repeats.
Physicochemical Information
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
Safety Information
Product Usage Statements
Usage Statement
  • Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
Storage and Shipping Information
Storage ConditionsReconstituted antibody can be stored at 2°-8°C for up to 12 months from date of receipt. Antibody can also be stored at -20°C in undiluted aliquots.
Packaging Information
Material Size50 µg
Transport Information
Supplemental Information
Specifications
Global Trade Item Number
Catalogue Number GTIN
CBL173 04053252468490

Documentation

Anti-Desmoplakin 1& 2 Antibody, clone DP2.15 SDS

Title

Safety Data Sheet (SDS) 

Anti-Desmoplakin 1& 2 Antibody, clone DP2.15 Certificates of Analysis

TitleLot Number
MOUSE ANTI-HUMAN DESMOPLAKIN 1 2 MONOCLONAL ANTIBODY - 2136580 2136580
MOUSE ANTI-HUMAN DESMOPLAKIN 1 & 2 2843082
MOUSE ANTI-HUMAN DESMOPLAKIN 1 & 2 MONOCLONAL ANTIBODY - 2366505 2366505
MOUSE ANTI-HUMAN DESMOPLAKIN 1 & 2 MONOCLONAL ANTIBODY - 2428482 2428482
MOUSE ANTI-HUMAN DESMOPLAKIN 1 & 2 - 2990640 2990640
MOUSE ANTI-HUMAN DESMOPLAKIN 1 & 2 - 3267323 3267323
MOUSE ANTI-HUMAN DESMOPLAKIN 1 & 2 - 3322368 3322368
MOUSE ANTI-HUMAN DESMOPLAKIN 1 & 2 - 3389383 3389383
MOUSE ANTI-HUMAN DESMOPLAKIN 1 & 2 - 3557980 3557980
MOUSE ANTI-HUMAN DESMOPLAKIN 1 & 2 - 3738479 3738479

References

Reference overviewPub Med ID
Immunocytochemical identification of epithelium-derived human tumors with antibodies to desmosomal plaque proteins.
Franke, W W, et al.
Proc. Natl. Acad. Sci. U.S.A., 80: 543-7 (1983)  1983

Show Abstract
6340102 6340102

Data Sheet

Title
MOUSE ANTI-HUMAN DESMOPLAKIN 1 & 2 MONOCLONAL ANTIBODY