Mouse EDAR Antibody Summary
Glu27-Ala187
Accession # Q9R187
Applications
Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website.
Reconstitution Calculator
Preparation and Storage
- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Background: EDAR
EDAR is a type I transmembrane protein which is a member of the TNF Receptor Superfamily (TNFRSF). The extracellular domain contains 14 cysteine residues, six of which approximate the TNFRSF cysteine-rich region, the cytoplasmic domain contains a region with homology to the death domains found in other TNFRSF members. Mouse EDAR is a 488 amino acid (aa) protein with a predicted 30 aa signal, a 159 aa extracellular domain, a 22 aa transmembrane domain, and a 277 aa cytoplasmic domain. The human and mouse EDAR homologs share 91% identity. Within the TNFRSF, EDAR shares the highest homologies with XEDAR and TNFRSF19/TROY. EDA-A1 is the EDAR ligand. EDA and EDAR have been associated with hypohidrotic ectodermal dysplasia (HED). HED is characterized by abnormalities in hair, teeth and eccrine sweat gland morphogenesis. HED was initially found to associate with two gene loci, tabby and downless. Tabby was later identified as the gene for EDA and downless as the autosomal EDAR gene. EDA has two splice variants, EDA-A1 and EDA-A2 which differ by only two amino acids. Despite this minor difference, the EDA isoforms display strong receptor specificity. EDA-A1 only binds to EDAR, whereas EDA-A2 binds to XEDAR, an X-linked TNFRSF member with high homology to EDAR. Mutations in EDA, EDAR and XEDAR have been associated with HED.
- Headon, D.J. and Overbeek, P.A. (1999) Nat. Genet. 22:370.
- Kumar, A. et al. (2000) J. Biol. Chem. 276:2668.
- Monreal, A.W. et al. (1999) Nat. Genet. 22:366.
- Schneider, P. et al. (2001) J. Biol. Chem. 276:18819.
- Srivastava, A.K. et al. (1997) Proc. Natl. Acad. Sci. USA 94:13069.
- Yan, M. et al. (2000) Science 209:523.
Product Datasheets
Citations for Mouse EDAR Antibody
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.
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Citations: Showing 1 - 6
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Generation and characterization of hair-bearing skin organoids from human pluripotent stem cells
Authors: J Lee, WH van der Va, SA Serdy, C Deakin, J Kim, AP Le, KR Koehler
Nature Protocols, 2022-03-23;0(0):.
Species: Mouse
Sample Types: Whole Tissue
Applications: IHC -
Polycomb repressive complex 2 in adult hair follicle stem cells is dispensable for hair regeneration
Authors: P Flora, MY Li, PM Galbo, M Astorkia, D Zheng, E Ezhkova
PloS Genetics, 2021-12-14;17(12):e1009948.
Species: Transgenic Mouse
Sample Types: Whole Tissue
Applications: IHC -
Differentiated Daughter Cells Regulate Stem Cell Proliferation and Fate through Intra-tissue Tension
Authors: Wenxiu Ning, Andrew Muroyama, Hua Li, Terry Lechler
Cell Stem Cell
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Dermal Condensate Niche Fate Specification Occurs Prior to Formation and Is Placode Progenitor Dependent
Authors: Ka-Wai Mok, Nivedita Saxena, Nicholas Heitman, Laura Grisanti, Devika Srivastava, Mauro J. Muraro et al.
Developmental Cell
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Nicotinic receptor Alpha7 expression during tooth morphogenesis reveals functional pleiotropy.
Authors: Rogers SW, Gahring LC
PLoS ONE, 2012-05-30;7(5):e36467.
Species: Mouse
Sample Types: Whole Tissue
Applications: IHC-Fr -
Involvement of the Edar signaling in the control of hair follicle involution (catagen).
Authors: Fessing MY, Sharova TY, Sharov AA, Atoyan R, Botchkarev VA
Am. J. Pathol., 2006-12-01;169(6):2075-84.
Species: Mouse
Sample Types: Tissue Homogenates, Whole Tissue
Applications: IHC-Fr, Western Blot
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