Arylsulfatase K Polyclonal Antibody, 50ul Plates & Dishes Defects in this gene are

Defects in this gene are the cause of hemochromatosis type 2A

Mutations in this gene cause various glaucoma phenotypes including primary congenital glaucoma

and non-small cell lung cancers

NDUFB1 (NADH: ubiquinone Oxidoreductase Subunit B1) is a Protein Coding gene

This gene encodes one of several alternate regulatory subunits of serine/threonine protein phosphatase 4 (PP4)

Arylsulfatase K Polyclonal Antibody, 50ul Plates & Dishes Defects in this gene areSulfatases (EC 3. . ), such as ARSK, hydrolyze sulfate esters from sulfated steroids, carbohydrates, proteoglycans, and glycolipids. They are involved in hormone biosynthesis, modulation of cell signaling, and degradation of macromolecules (Sardiello et al. 2005 [PubMed 16174644]).