FAM3B Polyclonal Antibody, 20ul Antibody Humanization G3BP2 has been shown to

G3BP2 has been shown to interact with IκBα

Defects in this gene are a cause of chromosome 9q subtelomeric deletion syndrome (9q-syndrome

Two key tumor suppressor genes are associated with chromosome 17

COMT is found in two forms in tissues

and different kinds of catalytic activities

FAM3B Polyclonal Antibody, 20ul Antibody Humanization G3BP2 has been shown toHas delayed effects on beta cell function, inhibiting basal insulin secretion from a beta cell line in a dose dependent manner.,miscellaneous: 2 N termini have been observed in the mature protein: the first at Glu 30, resulting from signal peptide cleavage, the second at Ser 46.,Belongs to the FAM3 family.,subcellular location: Localized in discrete vesicular and perinuclear structure.,tissue specificity: Highly expressed in the pancreas. Also found