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

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

Mutations in NODAL are associated with heterotaxy

This gene encodes an intracellular tyrosine kinase expressed in T-cells

The proteins of this family form hetero- or homodimers and act as anti- and pro-apoptotic regulators that are involved in a wide variety of cellular activities such as embryonic development

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