FAM3B Polyclonal Antibody, 20ul Antibody Humanization Defects in this gene are

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

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

Two key tumor suppressor genes are associated with chromosome 17

which is one of the three key genes associated with the development of Alzheimer's disease (AD)

FAM3B Polyclonal Antibody, 20ul Antibody Humanization Defects in this gene areHas 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