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Phospholipid translocation seems also to be implicated in vesicle formation and in uptake of lipid signaling molecules

Mutations in this gene have been associated with Specific Granule Deficiency

Peroxisomal multifunctional enzyme type 2 encoded by HSD17B4 is a bifunctional enzyme that is involved in the peroxisomal beta-oxidation pathway for fatty acids

and tropomyosin

DRP1 Polyclonal Antibody, 20ul Enzymes Elevate your lab work withDNM1L encodes a member of the dynamin superfamily of GTPases. Dynamin 1 like 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