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

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

It is known to complex with integrins

It is sensitive to brefeldin A

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

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