Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
Show all species
Show all synonyms
Select your species and application
anti-Human Desmoglein 1 Antibodies:
anti-Rat (Rattus) Desmoglein 1 Antibodies:
anti-Mouse (Murine) Desmoglein 1 Antibodies:
Go to our pre-filtered search.
Human Monoclonal Desmoglein 1 Primary Antibody for IHC (fro), IF - ABIN2473329
Zientarski: A rare variation of the extensor indicis muscle. in Folia morphologica 1977
Show all 4 Pubmed References
Human Polyclonal Desmoglein 1 Primary Antibody for ELISA, IHC - ABIN4305008
Nilles, Parry, Powers, Angst, Wagner, Green: Structural analysis and expression of human desmoglein: a cadherin-like component of the desmosome. in Journal of cell science 1992
Human Monoclonal Desmoglein 1 Primary Antibody for FACS, IF - ABIN5576848
Wahl: Generation of monoclonal antibodies specific for desmoglein family members. in Hybridoma and hybridomics 2002
Study identified DSG1 to be involved in the progressive intestinal injury associated with the development of Crohn's Disease complications via its effect on intestinal cell adhesion.
The authors report one recurrent and five novel DSG1 mutations, causing varying patterns of PPK (show GJB2 Antibodies), highlighting the clinical heterogeneity arising from mutations in this gene.
Authors report a new family of severe dermatitis, multiple allergies and metabolic wasting syndrome of Asian decent and expand the spectrum of mutations in the DSG1 gene.
Case Report: striate palmoplantar keratoderma showing transgrediens in a patient with heterozygote nonsense mutations in DSG1 and SERPINB7 (show SERPINB7 Antibodies).
Genetic deletion of sdrD in S. aureus NCTC8325-4 through allelic replacement resulted in decreased bacterial adherence to Dsg1- expressing HaCaT cells in vitro.
The results of this study describes the fourth family with a biallelic mutation in the DSG1 gene associated with SAM (show TTN Antibodies) syndrome, and emphasizes that the presence of PPK (show GJB2 Antibodies) and skin fragility with or without additional symptoms should alert clinicians to consider DSG1 deficiency.
Desmoglein 1 mutation as cause of SAM (show TTN Antibodies) syndrome
Oxidized low-density lipoprotein attenuated desmoglein 1 and desmocollin 2 (show DSC2 Antibodies) expression in human umbilical vein endothelial cells.
Desmoglein-1 regulates esophageal epithelial barrier function and immune responses in eosinophilic esophagitis.
Ectopic expression of Dsg1 in keratinocyte monolayers rescued the UVB-induced differentiation defect
The study indicated a possible correlation between the genotypes of two out of seven SNPs found in the porcine desmoglein 1 gene and the susceptibility to exudative epidermitis.
Transgenic expression of Dsg1 rescued the severe B6-Dsg3 (show DSG3 Antibodies)(-/-) phenotype and provided a syngeneic mouse model of pemphigus vulgaris (show DSG3 Antibodies).
Staphylococcal exfoliative toxins act as serine proteases with extremely focused molecular specificity to cleave mouse and human desmoglein 1 (Dsg1) once after glutamic acid residue 381 between extracellular domains 3 and 4.
Expression of desmoglein 1 compensates for genetic loss of desmoglein 3 (show DSG3 Antibodies) in keratinocyte adhesion.
Component of intercellular desmosome junctions. Involved in the interaction of plaque proteins and intermediate filaments mediating cell-cell adhesion.
, cadherin family member 4
, desmosomal glycoprotein 1
, pemphigus foliaceus antigen
, desmoglein 1 beta
, desmoglein 1 gamma
, desmosomal glycoprotein I