Full Product Name
DSG2 Antibody
Product Synonym Names
HDGC; CDHF5; ARVC10; ARVD10; CMD1BB
Product Gene Name
anti-DSG2 antibody
[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
3D Structure
ModBase 3D Structure for Q14126
Specificity
The antibody detects endogenous levels of total DSG2 protein.
Purity/Purification
Antigen affinity purification.
Form/Format
Rabbit IgG in pH7.3 PBS, 0.05% NaN3, 50% Glycerol.
Concentration
2 mg/ml (lot specific)
Immunogen Type
Recombinant Protein
Immunogen Description
Fusion protein corresponding to residues near the C terminal of human desmoglein 2
Preparation and Storage
Store at -20 degree C
Other Notes
Small volumes of anti-DSG2 antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Related Product Information for
anti-DSG2 antibody
Desmosomes are cell-cell junctions between epithelial, myocardial, and certain other cell types. This gene product is a calcium-binding transmembrane glycoprotein component of desmosomes in vertebrate epithelial cells. Currently, three desmoglein subfamily members have been identified and all are members of the cadherin cell adhesion molecule superfamily. These desmoglein gene family members are located in a cluster on chromosome 18. This second family member is expressed in colon, colon carcinoma, and other simple and stratified epithelial-derived cell lines.
Product Categories/Family for anti-DSG2 antibody
Total protein Ab
Applications Tested/Suitable for anti-DSG2 antibody
Immunohistochemistry (IHC)
Application Notes for anti-DSG2 antibody
Immunohistochemistry: 1:50-1:200
Immunohistochemistry (IHC) of anti-DSG2 antibody
Immunohistochemical analysis of paraffin-embedded Human breast cancer tissue using at dilution 1/50.

Immunohistochemistry (IHC) of anti-DSG2 antibody
Immunohistochemical analysis of paraffin-embedded Human gastric cancer tissue using at dilution 1/50.

NCBI/Uniprot data below describe general gene information for DSG2. It may not necessarily be applicable to this product.
NCBI Accession #
NP_001934.2
[Other Products]
NCBI GenBank Nucleotide #
NM_001943.3
[Other Products]
UniProt Primary Accession #
Q14126
[Other Products]
UniProt Secondary Accession #
Q4KKU6[Other Products]
UniProt Related Accession #
Q14126[Other Products]
Molecular Weight
122,294 Da
NCBI Official Full Name
desmoglein-2 preproprotein
NCBI Official Synonym Full Names
desmoglein 2
NCBI Official Symbol
DSG2??[Similar Products]
NCBI Official Synonym Symbols
HDGC; CDHF5; ARVC10; ARVD10; CMD1BB
??[Similar Products]
NCBI Protein Information
desmoglein-2
UniProt Protein Name
Desmoglein-2
UniProt Synonym Protein Names
Cadherin family member 5; HDGC
Protein Family
Desmoglein
UniProt Gene Name
DSG2??[Similar Products]
UniProt Synonym Gene Names
CDHF5??[Similar Products]
UniProt Entry Name
DSG2_HUMAN
NCBI Summary for DSG2
Desmosomes are cell-cell junctions between epithelial, myocardial, and certain other cell types. This gene product is a calcium-binding transmembrane glycoprotein component of desmosomes in vertebrate epithelial cells. Currently, three desmoglein subfamily members have been identified and all are members of the cadherin cell adhesion molecule superfamily. These desmoglein gene family members are located in a cluster on chromosome 18. This second family member is expressed in colon, colon carcinoma, and other simple and stratified epithelial-derived cell lines. Mutations in this gene have been associated with arrhythmogenic right ventricular dysplasia, familial, 10. [provided by RefSeq, Jul 2008]
UniProt Comments for DSG2
DSG2: Component of intercellular desmosome junctions. Involved in the interaction of plaque proteins and intermediate filaments mediating cell-cell adhesion. Defects in DSG2 are the cause of familial arrhythmogenic right ventricular dysplasia type 10 (ARVD10); also known as arrhythmogenic right ventricular cardiomyopathy 10 (ARVC10). 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. Genetic variations in DSG2 are the cause of susceptibility to cardiomyopathy dilated type 1BB (CMD1BB). A disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death.
Protein type: Membrane protein, integral; Calcium-binding; Cell adhesion
Chromosomal Location of Human Ortholog: 18q12.1
Cellular Component: desmosome; cell surface; apical plasma membrane; plasma membrane; integral to membrane; intercellular junction; lateral plasma membrane
Molecular Function: calcium ion binding
Biological Process: maternal process involved in pregnancy; apoptosis; homophilic cell adhesion; cell adhesion; response to progesterone stimulus; cell structure disassembly during apoptosis
Disease: Cardiomyopathy, Dilated, 1bb; Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
Research Articles on DSG2
1. In endometrial luminal epithelium, cadherin 6, desmoglein 2 and plexin b2 were surprisingly found in the apical as well as the lateral membrane domain; their knock-down compromised epithelial integrity.
Precautions
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Disclaimer
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