The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
Use a concentration of 1 - 2 µg/ml. Predicted molecular weight: 46 kDa.
Use a concentration of 20 µg/ml.
Use at an assay dependent concentration.
Use a concentration of 2.5 µg/ml.
FunctionCatalyzes the initial step in the synthesis of dolichol-P-P-oligosaccharides.
PathwayProtein modification; protein glycosylation.
Involvement in diseaseDefects in DPAGT1 are the cause of congenital disorder of glycosylation type 1J (CDG1J) [MIM:608093]. CDGs are a family of severe inherited diseases caused by a defect in protein N-glycosylation. They are characterized by under-glycosylated serum proteins. These multisystem disorders present with a wide variety of clinical features, such as disorders of the nervous system development, psychomotor retardation, dysmorphic features, hypotonia, coagulation disorders, and immunodeficiency. The broad spectrum of features reflects the critical role of N-glycoproteins during embryonic development, differentiation, and maintenance of cell functions.
Sequence similaritiesBelongs to the glycosyltransferase 4 family.