REPS1 Polyclonal Antibody, 100ul Lentiviral Packaging Mutations in this gene are

Mutations in this gene are associated with prolonged electroretinal response suppression (PERRS)| also known as bradyopsia

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

two epsilon chains together with two alpha chains form the embryonic Hb Gower II

Ena-VASP family members contain an EHV1 N-terminal domain that binds proteins containing E/DFPPPPXD/E motifs and targets Ena-VASP proteins to focal adhesions

REPS1 Polyclonal Antibody, 100ul Lentiviral Packaging Mutations in this gene areREPS1 (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