EDA Polyclonal Antibody | E-AB-11176

EDA Polyclonal Antibody | E-AB-11176 | Gentaur UK, US & Europe Distribution

Type: Polyclonal Antibody

Synonyms: ECTD1, Ectodermal dysplasia 1, anhidrotic, Ectodermal dysplasia protein, Ectodermal dysplasia, anhidrotic (hypohydrotic), Ectodysplasin A, Ectodysplasin A, membrane form, Ectodysplasin A, secreted form, ECTODYSPLASIN A1 ISOFORM, ECTODYSPLASIN A2 ISOFORM, ECTODYSPLASIN, Ectodysplasin-A, ED1 A1, ED1 A2, ED1, ED1 GENE, Eda A1, Eda A2, eda, EDA protein, EDA protein homolog, EDA, EDA1, EDA1 GENE, EDA2, HED, HED1, ODT1, Oligodontia 1, secreted form, STHAGX1, Ta, Tabby, Tabby protein, X linked anhidroitic ectodermal dysplasia protein, XHED, XLHED

Application: IHC, ELISA

Reactivity: Human, Mouse

Host: Rabbit

Isotype: IgG

Reserch Areas: Developmental Biology, Signal Transduction, Stem Cells

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.

Concentration: 0.6 mg/mL

Storage: Store at -20°C. Avoid freeze / thaw cycles.

Immunogen: Recombinant protein of human EDA

Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4

Purification Method: Affinity purification

Dilution: IHC 1:50-1:200

Clone: N/A

Conjugation: Unconjugated

Molecular Weight(Calculated): N/A

Molecular Weight(Observed): N/A