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

and contiguous with the luteinizing hormone beta subunit gene

COMT is found in two forms in tissues

The lack of RFX binding activity in complementation group C results from mutations in the RFX5 gene encoding the 75-kD subunit of RFX (Steimle et al

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