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results suggest that the metabolism of CYP4F11 substrates may be reduced in individuals carrying the CYP4F11 D315N genetic variant and individuals carrying the common D446N CYP4F11 variant likely exhibit comparable 20-HETE synthesis as individuals expressing wild-type CYP4F11.
Microsomal menaquinone-4 omega-hydroxylation activities correlated with the CYP4F2 (show CYP4F2 Antibodies) V433M genotype but not the CYP4F11 D446N genotype
The CYP4F11 gene is positively regulated by multiple signaling pathways in HaCaT keratinocytes, including retinoid X receptor (show RXRB Antibodies) and JNK (show MAPK8 Antibodies) signaling pathways.
3-hydroxystearate and 3-hydroxypalmitate are converted to omega-hydroxylated 3-OHDCA precursors in liver; CYP4F11 and, to a lesser extent, CYP4F2 (show CYP4F2 Antibodies) catalyzed omega-hydroxylation of 3-hydroxystearate; CYP4F3b, CYP4F12 (show CYP4F12 Antibodies), and CYP4A11 (show CYP4A11 Antibodies) had negligible activity.
This gene, CYP4F11, 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 gene is part of a cluster of cytochrome P450 genes on chromosome 19. Another member of this family, CYP4F2, is approximately 16 kb away. Alternatively spliced transcript variants encoding the same protein have been found for this gene.
cytochrome P450 4F11
, cytochrome P450, subfamily IVF, polypeptide 11