ADA15 Polyclonal Antibody, 20ul Monoclonal Antibodies Mutations in this gene are

Mutations in this gene are associated with the French-Canadian type of Leigh syndrome

This is a rabbit polyclonal antibody raised against the C terminus of human CEP97

Serves as a positive regulator of erythroid differentiation

It functions as a calcium-dependent nucleotidase with a preference for UDP

Nucleocytoplasmic transport

ADA15 Polyclonal Antibody, 20ul Monoclonal Antibodies Mutations in this gene areThe 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