EDA Polyclonal Antibody, 50ul Reagent Reservoirs a N-terminal I-band and a

a N-terminal I-band and a C-terminal A-band

Mutations in this gene result in malonyl-CoA decarboyxlase deficiency

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

RPS18 (ribosomal protein S18) encodes a ribosomal protein that is a component of the 40S subunit

EDA Polyclonal Antibody, 50ul Reagent Reservoirs a N-terminal I-band and aThe 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