CYFP1 Polyclonal Antibody, 50ul[BT-AP15151] Protein Post-translational Modification Mutations in this gene are

Mutations in this gene are associated with Keppen-Lubinsky Syndrome| a rare condition characterized by severe developmental delay| facial dysmorphism| and intellectual disability

an autosomal dominant disorder characterized by numerous small white flecks present in all layers of the corneal stroma

CTNNA1 encodes a member of the catenin family of proteins that play an important role in cell adhesion process by connecting cadherins located on the plasma membrane to the actin filaments inside the cell

characterized by a LIM motif and a domain of Src homology region 3

CYFP1 Polyclonal Antibody, 50ul[BT-AP15151] Protein Post-translational Modification Mutations in this gene areInvolved in formation of membrane ruffles and lamellipodia protrusions and in axon outgrowth. Binds to F actin but not to RNA.,Belongs to the CYFIP family.,subcellular location: Highly expressed in the perinuclear region. Enriched in synaptosomes, membrane ruffles and at the tips of lamellipodia.,subunit: Interacts with the active GTP bound form of RAC1. Interacts with FMR1 FMRP but does not bind to related proteins FXR1 or FXR2. Component of the