MDR3 Polyclonal Antibody, 100ul Reagent Reservoirs identified in the human major

identified in the human major histocompatibility complex class I region

galactoside binding soluble 3 is characterized by an N-terminal proline-rich tandem repeat domain and a single C-terminal carbohydrate recognition domain

neuronal growth cone collapse and cell migration

Defects in this gene are the cause of Werner syndrome| an autosomal recessive disorder characterized by premature aging

MDR3 Polyclonal Antibody, 100ul Reagent Reservoirs identified in the human majorThe membrane associated protein encoded by this gene is a member of the superfamily of ATP binding cassette (ABC) transporters. ABC proteins transport various molecules across extra and intra cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR TAP subfamily. Members of the MDR TAP subfamily are involved in multidrug resistance as well as antigen