EDA Polyclonal Antibody, 50ul Reagent Reservoirs Mutations in this gene result

Mutations in this gene result in malonyl-CoA decarboyxlase deficiency

site 1) encodes a member of the subtilisin-like proprotein convertase family

It has been suggested that the polymorphism of these genes is associated with rheumatoid arthritis and Alzheimer's disease

This protein acts as part of a multisubunit complex which includes histone deacetylases to modify chromatin structure that prevents basal transcriptional activity of target genes

induction:In hepatoblastoma HepG2 cells

EDA Polyclonal Antibody, 50ul Reagent Reservoirs Mutations in this gene resultThe protein encoded by EDA (ectodysplasin A) 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 EDA are a cause of ectodermal dysplasia, anhidrotic, which is also known as X linked hypohidrotic ectodermal dysplasia. Several