PSG8 Rabbit Polyclonal Antibody, 50ul Cell Transfection Mutations and deficiencies in this

Mutations and deficiencies in this protein have been observed in patients with hyperinsulinemic hypoglycemia of infancy| an autosomal recessive disorder of unregulated and high insulin secretion

which enhances the ubiquitination activity of SCF

the existence of such form has not been clearly demonstrated

SLC22A18 is imprinted

but the full-length nature of only three are known

PSG8 Rabbit Polyclonal Antibody, 50ul Cell Transfection Mutations and deficiencies in thisThe human pregnancy specific glycoproteins (PSGs) are a group of molecules that are mainly produced by the placental syncytiotrophoblasts during pregnancy. PSGs comprise a subgroup of the carcinoembryonic antigen (CEA) family which belongs to the immunoglobulin superfamily. For additional general information about the PSG gene family see PSG1 (MIM 176390).