Fgl2 Polyclonal Antibody, 50ul Metabolic enzymes Defects in this gene are

Defects in this gene are a cause of Pitt-Hopkins syndrome

and other types of diseases

Belongs to the cation transport ATPase (P-type) family

hypomethylation of the CAGE promoter region is associated with tumor progression and may serve as a valuable marker in cancer diagnosis

Fgl2 Polyclonal Antibody, 50ul Metabolic enzymes Defects in this gene areFibroleukin encoded by FGL2 is a secreted protein that is similar to the beta and gamma chains of fibrinogen. The carboxyl terminus of the encoded protein consists of the fibrinogen related domains (FRED). The encoded protein forms a tetrameric complex which is stabilized by interchain disulfide bonds. This protein may play a role in physiologic functions at mucosal sites.