This gene is a member of the lipoma HMGIC fusion partnern(LHFP) gene family, which is a subset of the superfamily ofntetraspan transmembrane protein encoding genes. Mutations in thisngene result in deafness in humans, and a mutation in a similar genenin mice results in deafness and vestibular dysfunction with severendegeneration of the organ of Corti. It is proposed to function innhair bundle morphogenesis.
应用类型
WB
免疫原
This LHFPL5 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 186-214 amino acids from the C-terminal region of human LHFPL5.
