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Overview
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DRP1 is a protein encoded by the DNM1L gene which is approximately 81, 8 kDa. DRP1 is localised to the cytoplasm and Golgi apparatus. It is involved in toll-like receptor signalling pathways, the TNF signalling pathway, cytoskeletal signalling and apoptotic cleavage of cellular proteins. This protein falls under the dynamin superfamily of GTPases. It mediates mitochondrial and peroxisomal division, and is involved in developmentally regulated apoptosis and programmed necrosis. DRP1 is expressed ubiquitously with the highest levels found in skeletal muscles, heart, kidney and brain. Mutations in the DNM1L gene may result in encephalopathy. STJ92779 was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen. This polyclonal antibody detects endogenous levels of DRP1 protein.
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Overview