This antibody detects endogenous protein at a molecular weight of 77 kDa.
Purity is >95% by SDS-PAGE.
GNPAT is a key enzyme located in the peroxisomal membrane which is essential to the synthesis of ether phospholipids. Mutations in GNPAT are associated with rhizomelic chondrodysplasia punctata type 2, which is characterized by rhizomelic shortening of femur and humerus, vertebral disorders, cataract, cutaneous lesions and severe mental retardation.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: acyl-CoA:dihydroxyacetonephosphate acyltransferase; Acyl-CoA:dihydroxyacetonephosphateacyltransferase; DAP-AT; DHAP-AT; Dihydroxyacetone phosphate acyltransferase; Glycerone-phosphate O-acyltransferase
Gene Aliases: AU019525; D1Ertd819e; DAP-AT; DAPAT; DHAPAT; GNPAT; RCDP2
Molecular Function: acyltransferase