GPX3 Polyclonal Antibody, 20ul Gene Editing Mutations in this gene have

Mutations in this gene have been associated with postmenopausal osteoporosis

Also removes gene-encoded polyglutamates from the carboxy-terminus of target proteins such as MYLK

Mutations in this gene are a cause of Cushing disease and adrenocortical hyperplasia

Mutations in NODAL are associated with heterotaxy

non-sterile

GPX3 Polyclonal Antibody, 20ul Gene Editing Mutations in this gene haveThe protein encoded by this gene belongs to the glutathione peroxidase family, members of which catalyze the reduction of organic hydroperoxides and hydrogen peroxide (H2O2) by glutathione, and thereby protect cells against oxidative damage. Several isozymes of this gene family exist in vertebrates, which vary in cellular location and substrate specificity. This isozyme is secreted, and is abundantly found in plasma. Downregulation of expression of