PED1A Rabbit Polyclonal Antibody, 100ul Isothermal Amplification |PTM:Prolines at the third position

|PTM:Prolines at the third position of the tripeptide repeating unit (G-X-Y) are hydroxylated in some or all of the chains

Mutations in this gene are associated with Jalili syndrome which consists of cone-rod dystrophy and amelogenesis imperfecta

Alternate splicing results in multiple transcript variants

Multifunctional protein working as a cell cycle progression factor as well as a cell survival factor

A pseudogene of this gene is found on chromosome X

PED1A Rabbit Polyclonal Antibody, 100ul Isothermal Amplification |PTM:Prolines at the third positionThe protein encoded by this gene is a member of the GDSL SGNH superfamily. Members of this family are hydrolytic enzymes with esterase and lipase activity and broad substrate specificity. This protein belongs to the Pmr5 Cas1p esterase subfamily in that it contains the catalytic triad comprised of serine aspartate and histidine and lacks two conserved regions (glycine after strand S2 and GxND motif). A pseudogene of this gene has been identified on