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DSG2 Monoclonal antibody, PBS Only

DSG2 Monoclonal Antibody for WB,Indirect ELISA

Host / Isotype

Mouse / IgG1

Reactivity

Human

Applications

WB,Indirect ELISA

Conjugate

Unconjugated

CloneNo.

1B8C3

Cat No : 68515-1-PBS

Print datasheet

Synonyms

ARVC10, ARVD10, Cadherin family member 5, CDHF5, desmoglein 2, DSG2, HDGC

验证数据展示

  • WB analysis using 68515-1-Ig (same clone as 68515-1-PBS)

    WB analysis using 68515-1-Ig (same clone as 68515-1-PBS)

    Various lysates were subjected to SDS PAGE followed by western blot with 68515-1-Ig (DSG2 antibody) at dilution of 1:5000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 68515-1-PBS in a different storage buffer formulation.

产品信息

68515-1-PBS targets DSG2 in WB, Indirect ELISA applications and shows reactivity with Human samples.

Tested Applications WB,Indirect ELISA
Tested Reactivity Human
Immunogen DSG2 fusion protein Ag20633 种属同源性预测
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Full Name desmoglein 2
Synonyms ARVC10, ARVD10, Cadherin family member 5, CDHF5, desmoglein 2, DSG2, HDGC
Calculated Molecular Weight 1118 aa, 122 kDa
Observed Molecular Weight145-150 kDa
GenBank Accession NumberBC099655
Gene Symbol DSG2
Gene ID (NCBI) 1829
Conjugate Unconjugated
Form Liquid
Purification MethodProtein G purification
UNIPROT IDQ14126
Storage Buffer PBS Only
Storage ConditionsStore at -80°C.

背景介绍

Desmosomes are cell-cell junctions between epithelial, myocardial, and certain other cell types. Desmosomal cadherins, consisting of four desmogleins (DSG1-4) and three desmocollins (DSC1-3) in humans, mediate adhesion through calcium-dependent homophilic/heterophilic interactions. DSG2 is a single-pass transmembrane glycoprotein that is widely expressed in epithelial and non-epithelial tissues, such as the intestine, epidermis, testis, and heart (PMID:21715983). Defects in DSG2 are the cause of familial arrhythmogenic right ventricular dysplasia type 10 (ARVD10), and genetic variations in DSG2 are the cause of susceptibility to cardiomyopathy dilated type 1BB (CMD1BB).