ELISA EDA anti-

Quantity :50µL Clone Number: Aliases:ECTD1 antibody; Ectodermal dysplasia 1; anhidrotic antibody; Ectodermal dysplasia protein antibody; Ectodermal dysplasia; anhidrotic (hypohydrotic) antibody; Ectodysplasin A antibody; Ectodysplasin A; membrane form antibody; Ectodysplasin A; secreted form antibody; ECTODYSPLASIN A1 ISOFORM antibody; ECTODYSPLASIN A2 ISOFORM antibody; ECTODYSPLASIN antibody; Ectodysplasin-A antibody; ED1 A1 antibody; ED1 A2 antibody; ED1 antibody; ED1 GENE antibody; Eda A1 antibody; Eda A2 antibody; eda antibody; EDA protein antibody; EDA protein homolog antibody; EDA_ antibody; EDA1 antibody; EDA1 GENE antibody; EDA2 antibody; HED antibody; HED1 antibody; ODT1 antibody; Oligodontia 1 antibody; secreted form antibody; STHAGX1 antibody; Ta antibody; Tabby antibody; Tabby protein antibody; X linked anhidroitic ectodermal dysplasia protein antibody; XHED antibody; XLHED antibody Product Type:Polyclonal Antibody Immunogen Species:Homo sapiens () UniProt ID:Q92838 Immunogen:Fusion protein of EDA Raised in:Rabbit Reactivity:, Mouse Tested Applications:ELISA, IHC; ELISA:1:2000-1:5000, IHC:1:50-1:200 Background:The protein encoded by this gene is a type II membrane protein that can be cleaved by furin to produce a secreted form. The encoded protein, which belongs to the tumor necrosis factor family, acts as a homotrimer and may be involved in cell-cell signaling during the development of ectodermal organs. Defects in this gene are a cause of ectodermal dysplasia, anhidrotic, which is also known as X-linked hypohidrotic ectodermal dysplasia. Several transcript variants encoding many different isoforms have been found for this gene. Clonality:Polyclonal Isotype:IgG Purification Method:Antigen affinity purification Conjµgate:Non-conjµgated Buffer:-20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol Form:Liquid Stroage:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze. Target Names:EDA Research Areas:Developmental biology;Signal transduction?Stem cells