SQRD Rabbit Polyclonal Antibody, 50ul Cell Culture Dishes Mutations and deficiencies in peroxisomal

Mutations and deficiencies in peroxisomal protein importing and peroxisome assembly lead to peroxisomal biogenesis disorders

REC8 (REC8 meiotic recombination protein) encodes a member of the kleisin family of SMC (structural maintenance of chromosome) protein partners

The protein encoded by PTGER3 (prostaglandin E receptor 3) is a member of the G-protein coupled receptor family

Expression of PTPRZ1 is restricted to the central nervous system (CNS)

It also may play a role in early intestinal development

SQRD Rabbit Polyclonal Antibody, 50ul Cell Culture Dishes Mutations and deficiencies in peroxisomalThe protein encoded by this gene may function in mitochondria to catalyze the conversion of sulfide to persulfides thereby decreasing toxic concencrations of sulfide. Alternative splicing results in multiple transcript variants that encode the same protein.