ADA15 Polyclonal Antibody, 50ul Enzymes Polymorphisms in this gene have

Polymorphisms in this gene have been associated with an increased risk of rheumatoid arthritis

tissue specificity:Expressed chiefly in non-neuronal tissues

Mutations in this gene cause cleft lip and palate/ectodermal dysplasia 1 syndrome (CLPED1) as well as non-syndromic cleft lip with or without cleft palate (CL/P)

Defects in EIF2B4 are a cause of leukoencephalopathy with vanishing white matter (VWM) and ovarioleukodystrophy

ADA15 Polyclonal Antibody, 50ul Enzymes Polymorphisms in this gene haveThe protein encoded by this gene is a member of the ADAM (a disintegrin and metalloproteinase) protein family. ADAM family members are type I transmembrane glycoproteins known to be involved in cell adhesion and proteolytic ectodomain processing of cytokines and adhesion molecules. This protein contains multiple functional domains including a zinc binding metalloprotease domain a disintegrin like domain as well as a EGF like domain. Through its