MDR3 Polyclonal Antibody, 100ul Reagent Reservoirs or amplified in a series

or amplified in a series of tumours including anaplastic large cell lymphomas

and thus induce the nuclear production of NF-kappaB

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

GO annotations related to this gene include oxidoreductase activity

Mutations in this gene cause Alexander disease

MDR3 Polyclonal Antibody, 100ul Reagent Reservoirs or amplified in a seriesThe 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