BECP1 Polyclonal Antibody, 50ul ROS/Nitric Oxide Detection Isoform 2 is expressed in

Isoform 2 is expressed in all examined tissues except in bone marrow

and autosomal recessive non-syndromic sensorineural type 53 deafness (DFNB53)

Mutations in this gene are associated with hereditary hemorrhagic telangiectasia

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

BECP1 Polyclonal Antibody, 50ul ROS/Nitric Oxide Detection Isoform 2 is expressed inBECN2 (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