Alkyldihydroxyacetonephosphate synthase, peroxisomal or AGPS neo-epitope is encoded by the gene AGPS. AGPS is a member of the FAD-binding oxidoreductase/transferase type 4 family and is an enzyme involved in ether lipid biosynthesis. Diseases associated with this gene include forms of Rhizomelic Chondrodysplasia Punctata.
ICC, IHC, WB
66 kDa processed (vs. 72 kDa unprocessed)
Synthetic peptide amino acids 59-67 (KARRAASAA, site of proteolytic processing for peroxisome import) of human AGPS (also known as Alkylglycerone-phosphate synthase, Peroxisomal alkyldihydroxyacetonephosphate synthase, Alkyl-DHAP synthase, Aging-associated gene 5 protein, Ads and AAG5, accession number O00116); Mouse: 100% identity (9/9 amino acids identical); Rat: 100% identity (9/9 amino acids identical)
Human, Mouse, Rat
Store at ≤ -20 C for long term storage. For short term storage, store at 2-8 C. For maximum recovery of product, centrifuge the vial prior to removing the cap.
Does not cross-react with unprocessed AGPS
These antibodies are to be used as research laboratory reagents and are not for use as diagnostic or therapeutic reagents in humans.