REPS1 Polyclonal Antibody, 100ul Lentiviral Packaging Defects in this gene likely

Defects in this gene likely are a cause of non-syndromic autosomal dominant hearing loss

This member functions as a modulatory subunit

It is sensitive to brefeldin A

The encoded protein is associated with angiogenesis| with potential roles in endothelial tube formation and the migration of endothelial cells

Claudins are integral membrane proteins that are components of the epithelial cell tight junctions

REPS1 Polyclonal Antibody, 100ul Lentiviral Packaging Defects in this gene likelyREPS1 (RALBP1 associated Eps domain containing 1) encodes a signaling adaptor protein with two EH domains that interacts with proteins that participate in signaling, endocytosis and cytoskeletal changes. The encoded protein has been found in association with intersectin 1 and Src homology 3 domain growth factor receptor bound 2 like (endophilin) interacting protein 1 when intersectin 1 was isolated from clathrin coated pits. The encoded protein has