DSG2 Monoklonaler Antikörper
DSG2 Monoklonal Antikörper für WB, Cytometric bead array, Indirect ELISA
Wirt / Isotyp
Maus / IgG1
Getestete Reaktivität
human
Anwendung
WB, Cytometric bead array, Indirect ELISA
Konjugation
Unkonjugiert
CloneNo.
1B8C3
Kat-Nr. : 68515-1-PBS
Synonyme
Geprüfte Anwendungen
Produktinformation
68515-1-PBS bindet in WB, Cytometric bead array, Indirect ELISA DSG2 und zeigt Reaktivität mit human
| Getestete Reaktivität | human |
| Wirt / Isotyp | Maus / IgG1 |
| Klonalität | Monoklonal |
| Typ | Antikörper |
| Immunogen | DSG2 fusion protein Ag20633 |
| Vollständiger Name | desmoglein 2 |
| Berechnetes Molekulargewicht | 1118 aa, 122 kDa |
| Beobachtetes Molekulargewicht | 145-150 kDa |
| GenBank-Zugangsnummer | BC099655 |
| Gene symbol | DSG2 |
| Gene ID (NCBI) | 1829 |
| Konjugation | Unkonjugiert |
| Form | Liquid |
| Reinigungsmethode | Protein-G-Reinigung |
| Lagerungspuffer | PBS only |
| Lagerungsbedingungen | Store at -80°C. 20ul Größen enthalten 0,1% BSA. |
Hintergrundinformationen
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).





