"DSG2" Related Products


Recombinant Human Desmoglein 2

Cat. No. : DSG2-1601H
Description : Desmoglein 2, also known as DSG2, is a human gene. Desmosomes are cell-cell junctions between epithelial, myocardial, and certain other cell types. Desmoglein 2 is a calcium-binding transmembrane glycoprotein component of desmosomes in vertebrate epithelial cells. It provides cellular adhesion and forces transduction by cell-to-cell anchorage. It also plays a role in embryonic stem cell proliferation.
Molecular Weight : The predicted molecular weight of Recombinant Human Desmoglein-2 is Mr 89 kDa. However, the actual molecular weight as observed by migration on SDS Page is Mr 115 kDa.
Source : NSO Cells.
Amino Acid Sequence : Human Desmoglein2 (Ala49 Gly608) - IEGRMD - Human IgG1 (Pro100 Lys330).
State Of Matter : Lyophilized.
Purity : >95% by SDS Page and analyzed by silver stain.
Formulation : This recombinant protein was 0.2 µm filtered and lyophilized from modified Dulbecco's phosphate buffered saline (1X PBS) pH 7.2-7.3 with no calcium, magnesium, or preservatives.
Endotoxin : <1.0 EU/µg as determined by the LAL method.
Biological Activity : The biological activity of Human DSG2 was determined by the ability of the immobilized protein to support the adhesion of BUD8 human skin fibroblast cells. When 3 x 104 cells are added to recombinant human Desmoglein 2 coated plates (10 μg/ml, 100 μl/well), approximately 50%-80% will adhere after 1 hour at 37°C.
Storage And Stability : This lyophilized protein is stable for six to twelve months when stored desiccated at -20°C to -70℃. After aseptic reconstitution, this protein may be stored at 2°C to 8°C for one month or at -20°C to -70°C in a manual defrost freezer. Avoid Repeated Freeze Thaw Cycles. See Product Insert for exact lot specific storage instructions.
Gene Name : DSG2 desmoglein 2 [ Homo sapiens ]
Synonyms : DSG2; desmoglein 2; HDGC; CDHF5; ARVC10; ARVD10; CMD1BB; MGC117034; MGC117036; MGC117037; Desmoglein-2
Gene ID : 1829
mRNA Refseq : NM_001943
Protein Refseq : NP_001934
MIM : 125671
UniProt ID : Q14126
Chromosome Location : 18q12.1
Pathway : Arrhythmogenic right ventricular cardiomyopathy (ARVC)
Function : calcium ion binding; protein binding

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