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CYP2U1 encodes a member of the cytochrome P450 superfamily of enzymes. Additionally we are shipping Cytochrome P450, Family 2, Subfamily U, Polypeptide 1 Antibodies (26) and Cytochrome P450, Family 2, Subfamily U, Polypeptide 1 Proteins (3) and many more products for this protein.
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This is the first formal report of pigmentary degenerative maculopathy associated with a CYP2U1 homozygous mutation
we identified two novel mutations in CYP2U1 in two unrelated Hereditary spastic paraplegia patients by whole exome sequencing
This is the first report of CYP2E1 (show CYP2E1 ELISA Kits) and CYP2U1 protein expression in human Amygdala.
Data suggest that the 3D model could be useful to identify other substrates of cytochrome P450 2U1 (CYP2U1) and help in understanding its physiologic roles.
The CYP2U1 gene shows a low mutation frequency in a general population of complicated hereditary spastic paraparesis
human cytochrome P450 2U1 oxidizes endogenous N-arachidonoylserotonin
CYP1B1 (show CYP1B1 ELISA Kits) and CYP2U1 were the only quantifiable CYPs in in freshly isolated human brain microvessels.
Genetic polymorphism of CYP2U1, a cytochrome P450 (show CYP ELISA Kits) involved in fatty acids hydroxylation.
CYP2U1 plays an important physiological role in fatty acid signaling processes in both cerebellum and thymus
This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This enzyme is a hydroxylase that metabolizes arachidonic acid, docosahexaenoic acid, and other long chain fatty acids.
cytochrome P450 2U1
, cytochrome P450, family 2, subfamily U, polypeptide 1
, spastic paraplegia 49
, cytochrome P450, 2u1