ST6GAL1 Polyclonal Antibody, 100ul Cell Biology DLG4/PSD95

DLG4/PSD95

a rare and lethal autosomal recessive disorder of early childhood

Mutations in this gene have been associated with insulin-dependent diabetes mellitus

Diseases associated with NCOA7 include brugada syndrome

Belongs to the HMG-CoA synthase family

ST6GAL1 Polyclonal Antibody, 100ul Cell Biology DLG4/PSD95This gene encodes a member of glycosyltransferase family 29. The encoded protein is a type II membrane protein that catalyzes the transfer of sialic acid from CMP sialic acid to galactose containing substrates. The protein, which is normally found in the Golgi but can be proteolytically processed to a soluble form, is involved in the generation of the cell surface carbohydrate determinants and differentiation antigens HB 6, CD75, and CD76. This gene