Recombinant DRP1 Monoclonal Antibody

This gene encodes a member of the dynamin superfamily of GTPases. The encoded protein mediates mitochondrial and peroxisomal division, and is involved in developmentally regulated apoptosis and programmed necrosis. Dysfunction of this gene is implicated in several neurological disorders, including Alzheimer's disease. Mutations in this gene are associated with the autosomal dominant disorder, encephalopathy, lethal, due to defective mitochondrial and peroxisomal fission (EMPF) . Alternative splicing results in multiple transcript variants encoding different isoforms.

DRP; DLP; DNM1L; DLP1; DRP1; DVLP; DYMPLE; EMPF; EMPF1; HDYNIV; Dnm1p/Vps1p-like protein (DVLP) ; dynamin 1 like; Dynamin family member proline-rich carboxyl-terminal domain less (Dymple) ; Dynamin-1-like protein; Dynamin-like protein; DLP1; DRP1; DVLP; DYMPLE; dynamin 1 like; EMPF; EMPF1; HDYNIV; Dnm1p/Vps1p-like protein; dnml1; Dynamin family member proline-rich carboxyl-terminal domain less; Dynamin like protein; Dynamin related protein 1; Dynamin-like protein 4; Dynamin-like protein IV; Dynamin-related protein 1; DYNIV 11; FLJ41912; VPS1