OXA1L Rabbit Polyclonal Antibody, 20ul Custom DNA Oligos Defects in this gene are

Defects in this gene are a cause of susceptibility to familial hypertrigliceridemia

Four transcript variants encoding three different isoforms have been found for this gene

EIF2B is involved in protein synthesis and exchanges GDP and GTP for its activation and deactivation

5-trisphosphate receptor type 1) encodes an intracellular receptor for inositol 1

Most PSGs have an arg-gly-asp (RGD) motif

OXA1L Rabbit Polyclonal Antibody, 20ul Custom DNA Oligos Defects in this gene areThis gene encodes an evolutionarily conserved protein that is localized to the inner mitochondrial membrane. The encoded protein is essential for the translocation of the N terminal tail of subunit 2 of cytochrome c oxidase and is involved in the assembly of the cytochrome c oxidase and ATPase complexes of the mitochondrial respiratory chain.