EDA-A1, Soluble Recombinant Protein | EDA recombinant protein

EDA-A1, Soluble, Recombinant, Human (Ectodysplasin-A, Ectodermal Dysplasia Protein)

Cat. Num. AAA637348

• Gene Names: EDA; ED1; HED; EDA1; EDA2; HED1; ODT1; XHED; ECTD1; XLHED; ED1-A1; ED1-A2; EDA-A1; EDA-A2; STHAGX1
• Purity: Highly Purified; >95% (SDS-PAGE)
• Synonyms: EDA-A1; Soluble; Recombinant; Human (Ectodysplasin-A; Ectodermal Dysplasia Protein); EDA recombinant protein

• Host: Human, E Coli
• Specificity: Binds to human and mouse EDAR (ectodysplasin-A1 receptor).
• Purity/Purification: Highly Purified; >95% (SDS-PAGE)
• Form/Format: Supplied as a lyophilized powder from a 0.2um filtered solution in PBS pH 7.2.
• Sequence: The extracellular domain of human EDA-A1 (aa 240-391) is fused at the N-terminus to a DYKDDDDK-tag.

• Preparation and Storage: Short-term Storage: +4 degree C; Long-term Storage: -20 degree C; Stable for at least 6 months after receipt when stored at -20 degree C.

Related Product Information for EDA recombinant protein

EDA is involved in epithelial-mesenchymal signaling during morphogenesis of ectodermal organs. It binds to the receptor EDAR.

Product Categories/Family for EDA recombinant protein

Molecular Biology; MB-Disease Markers

NCBI and Uniprot Product Information

• NCBI GI #: 54112101
• NCBI GeneID: 1896
• NCBI Accession #: NP_001005609.1
• NCBI GenBank Nucleotide #: NM_001005609.1
• UniProt Accession #: Q92838; O75910; Q5JS00; Q5JUM7; Q9UP77; Q9Y6L0; Q9Y6L1; Q9Y6L2; A0AUZ2; A2A337; B7ZLU2; B7ZLU4
• Molecular Weight: ~19kD (SDS-PAGE)
• NCBI Official Full Name: ectodysplasin-A isoform 2
• NCBI Official Synonym Full Names: ectodysplasin A
• NCBI Official Symbol: EDA
• NCBI Official Synonym Symbols: ED1; HED; EDA1; EDA2; HED1; ODT1; XHED; ECTD1; XLHED; ED1-A1; ED1-A2; EDA-A1; EDA-A2; STHAGX1
• NCBI Protein Information: ectodysplasin-A; oligodontia 1; X-linked anhidroitic ectodermal dysplasia protein
• UniProt Protein Name: Ectodysplasin-A
• Protein Family: Ectodysplasin
• UniProt Gene Name: EDA
• UniProt Synonym Gene Names: ED1; EDA2; EDA protein
• UniProt Entry Name: EDA_HUMAN

NCBI Description

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. [provided by RefSeq, Jul 2008]

Uniprot Description

EDA: Seems to be involved in epithelial-mesenchymal signaling during morphogenesis of ectodermal organs. Isoform 1 binds only to the receptor EDAR, while isoform 3 binds exclusively to the receptor XEDAR. Defects in EDA are the cause of ectodermal dysplasia type 1 (ED1); also known as Christ-Siemens-Touraine syndrome or X-linked hypohidrotic ectodermal dysplasia (XLHED). Ectodermal dysplasia defines a heterogeneous group of disorders due to abnormal development of two or more ectodermal structures. ED1 is a disease characterized by sparse hair (atrichosis or hypotrichosis), abnormal or missing teeth and the inability to sweat due to the absence of sweat glands. ED1 is the most common form of over 150 clinically distinct ectodermal dysplasias. Defects in EDA are the cause of tooth agenesis selective X-linked type 1 (STHAGX1). A form of selective tooth agenesis, a common anomaly characterized by the congenital absence of one or more teeth. Selective tooth agenesis without associated systemic disorders has sometimes been divided into 2 types: oligodontia, defined as agenesis of 6 or more permanent teeth, and hypodontia, defined as agenesis of less than 6 teeth. The number in both cases does not include absence of third molars (wisdom teeth). Belongs to the tumor necrosis factor family. 8 isoforms of the human protein are produced by alternative splicing.

Protein type: Membrane protein, integral; Receptor, misc.; Motility/polarity/chemotaxis

Chromosomal Location of Human Ortholog: Xq12-q13.1

Cellular Component: endoplasmic reticulum membrane; collagen; cytoskeleton; intracellular membrane-bound organelle; membrane; integral to plasma membrane; apical part of cell; integral to membrane; plasma membrane; extracellular region

Molecular Function: protein binding; tumor necrosis factor receptor binding; receptor binding

Biological Process: pigmentation; cell-matrix adhesion; ectoderm development; gene expression; positive regulation of NF-kappaB import into nucleus; immune response; signal transduction; cell differentiation; odontogenesis of dentine-containing teeth; activation of NF-kappaB transcription factor

Disease: Tooth Agenesis, Selective, X-linked, 1; Ectodermal Dysplasia 1, Hypohidrotic, X-linked