Fer Polyclonal Antibody, 50ul[BT-AP03193] sgRNA Oligos and renal and muscular defects

and renal and muscular defects

The protein encoded by this gene belongs to the Rab family

Defects in this gene are the cause of Werner syndrome| an autosomal recessive disorder characterized by premature aging

The encoded protein also associates with hepatocyte growth factor-regulated substrate to form the endosomal sorting complex required for transport-0 (ESCRT-0)

This protein is a retina-specific ABC transporter with N-retinylidene-PE as a substrate

Fer Polyclonal Antibody, 50ul[BT-AP03193] sgRNA Oligos and renal and muscular defectsTyrosine protein kinase Fer encoded by FER is a member of the FPS FES family of non transmembrane receptor tyrosine kinases. It regulates cell cell adhesion and mediates signaling from the cell surface to the cytoskeleton via growth factor receptors. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome X.