SKU: WP12071 Categories: ,

Dsg1 Polyclonal Antibody

Price range: $268.00 through $328.00

SKU: WP12071-100
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Product details

Background:

This gene encodes a member of the desmoglein protein subfamily. Desmogleins, along with desmocollins, are cadherin-like transmembrane glycoproteins that are major components of the desmosome. Desmosomes are cell-cell junctions that help resist shearing forces and are found in high concentrations in cells subject to mechanical stress. This gene is found in a cluster with other desmoglein family members on chromosome 18. The encoded protein has been identified as a target of auto-antibodies in the autoimmune skin blistering disease pemphigus foliaceus. Disruption of this gene has also been associated with the skin diseases palmoplantar keratoderma and erythroderma. [provided by RefSeq, Feb 2015],

Specifications

Size50μL/100μL
TargetDsg1
ReactivityHuman, Mouse
ApplicationsWB, ELISA
MW(Calculated)
MW(Observed)114kD
Host SpeciesRabbit
IsotypeIgG
Conjugate/ModificationUnmodified
Recommended Dilution RatioWB 1:500-1:2000; ELISA 1:40000; Not yet tested in other applications.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration1 mg/ml
ClonalityPolyclonal
Clone Number
ImmunogenThe antiserum was produced against synthesized peptide derived from human DSG1. AA range:161-210
SpecificityDsg1 Polyclonal Antibody detects endogenous levels of Dsg1 protein.
Gene NameDSG1 CDHF4
Protein NameDesmoglein-1
Other NameDSG1; / CDHF4; / Desmoglein-1; / Cadherin family member 4; / Desmosomal glycoprotein 1; / DG1; / DGI; / Pemphigus foliaceus antigen
SpeciesHuman
Gene ID1828
UniprotQ02413
Species.1
Gene ID.1
Uniprot.1
Species.2
Gene ID.2
Uniprot.2
Cellular LocalizationCell membrane; Single-pass type I membrane protein . Cell junction, desmosome.
Tissue ExpressionEpidermis, tongue, tonsil and esophagus.
Signaling_pathway
Research Areas>>Staphylococcus aureus infection
FunctionDisease:Defects in DSG1 are the cause of palmoplantar keratoderma striate type 1 (SPPK1) [MIM:148700]; also known as keratosis palmoplantaris striata I. SPPK1 is a dermatoligical disorder characterized by thickening of the skin on the palms and soles, and longitudinal hyperkeratotic lesions on the palms, running the length of each finger.,Domain:Calcium may be bound by the cadherin-like repeats .,Function:Component of intercellular desmosome junctions. Involved in the interaction of plaque proteins and intermediate filaments mediating cell-cell adhesion.,similarity:Contains 4 cadherin domains.,tissue specificity:Epidermis, tongue, tonsil and esophagus.,
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