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  2. Polyclonal

600-401-AZ0

EDA1 Antibody

Cannot supply to this region.

SKU:
600-401-AZ0
Additional Names:
Ectodysplasin A, Ectodermal dysplasia protein, ED1, ED1-A1, ED1-A2, EDA1, EDA2, EDA protein, HED, ODT1, STHAGX1, XHED, XLHED|EDA
Application:
ELISA, IHC, WB, IF
Concentration:
1 mg/ml
Physical State:
Liquid
Species Reactivity:
Human
Storage Conditions:
-20[o]C aliquoted. Aliquot. Avoid freeze/thaw cycles., 2-8[o]C diluted. Aliquot. Avoid freeze/thaw cycles.
Supplier:
Rockland Inc
Host:
Rabbit
Reactivities:
Human, Mouse, Rat
Buffer:
0.01 M Sodium Phosphate, 0.25 M Sodium Chloride
Immunogen:
Anti-EDA1 antibody was prepared from whole rabbit serum produced by repeated immunizations with an 19 amino acid peptide near the internal region of human EDA1.
Formulation:
0.01 M Sodium Phosphate, 0.25 M Sodium Chloride, pH 7.2
Uniprot:
Q92838
Synonyms:
ECTD1;Ectodermal dysplasia protein;ectodysplasin-A;ED1;ED1-A1;ED1-A2;EDA-A1;EDA-A2;EDA1;EDA2;HED;HED1;ODT1;oligodontia 1;STHAGX1;TNLG7C;tumor necrosis factor ligand 7C;X-linked anhidroitic ectodermal dysplasia protein;XHED;XLHED
Extra Details:
Ectodysplasin A (EDA1) is a member of the TNF-related ligand family involved in the early epithelial-mesenchymal interaction that regulates ectodermal appendage formation (1). It is a trimeric type II membrane protein that co-localizes with cytoskeletal structures at the lateral and apical surfaces of cells and can be expressed as eight alternatively spliced isoforms in hair follicles and in the epidermis of adult skin (2,3). EDAs are required during development, and loss or mutation of EDA1 results in a group of developmental disorders identified as ectodermal dysplasia type 1 (4,5).
Shipping Conditions:
Dry Ice