BECP1 Polyclonal Antibody, 50ul ROS/Nitric Oxide Detection Mutations in this gene are

Mutations in this gene are associated with hereditary hemorrhagic telangiectasia

disease:Defects in MT-ND4 are a cause of Leber hereditary optic neuropathy (LHON)

arterioles and vas deferens

but is not expressed in either B or T cells

The enzyme requires NAD(H) as a coenzyme| and is inhibited by inorganic phosphate

BECP1 Polyclonal Antibody, 50ul ROS/Nitric Oxide Detection Mutations in this gene areBECN2 (Beclin 2) is a Protein Coding gene. Among its related pathways are Autophagy Pathway and Kaposi's sarcoma associated herpesvirus infection. An important paralog of this gene is BECN1. Involved in 2 distinct lysosomal degradation pathways: acts as a regulator of autophagy and as a regulator of G protein coupled receptors turnover. Regulates degradation in lysosomes of a variety of G protein coupled receptors via its interaction with GPRASP1