LRSM1 Polyclonal Antibody, 50ul Contamination Detection & Removal MyBP family

MyBP family

EMR4P is a member of the EGF-TM7 receptor gene family which is thought to play a role in leukocyte adhesion and migration

Mutations in CBL are also the cause of Noonan syndrome-like disorder

subunit:Homotrimer or homotetramer

May be the cardiac P2Y receptor involved in the regulation of cardiac muscle contraction through modulation of L-type calcium currents

LRSM1 Polyclonal Antibody, 50ul Contamination Detection & Removal MyBP familyThis gene encodes a ring finger protein involved in a variety of functions, including regulation of signaling pathways and cell adhesion, mediation of self ubiquitylation, and involvement in cargo sorting during receptor endocytosis. Mutations in this gene have been associated with Charcot Marie Tooth disease. Multiple transcript variants encoding different isoforms have been identified for this gene.