PRX I Polyclonal Antibody, 100ul[BT-AP13338] NGS Oligos Choose LightNing™

Choose LightNing™

Alterations of this gene| including point mutations| insertions and deletions| cause factor IX deficiency| which is a recessive X-linked disorder| also called hemophilia B or Christmas disease

The protein encoded by this gene appears to be multifunctional

This gene is located in an intron of the FBXL13 gene on the opposite strand

This gene encodes a member of the alcohol dehydrogenase family

PRX I Polyclonal Antibody, 100ul[BT-AP13338] NGS Oligos Choose LightNing™This gene encodes a member of the peroxiredoxin family of antioxidant enzymes, which reduce hydrogen peroxide and alkyl hydroperoxides. The encoded protein may play an antioxidant protective role in cells, and may contribute to the antiviral activity of CD8(+) T cells. This protein may have a proliferative effect and play a role in cancer development or progression. Four transcript variants encoding the same protein have been identified for this gene.