CD58 Polyclonal Antibody, 100ul[BT-AP02394] Lysosome Defects in EIF2B4 are a

Defects in EIF2B4 are a cause of leukoencephalopathy with vanishing white matter (VWM) and ovarioleukodystrophy

The protein encoded by this gene belongs to the SECY/SEC61- alpha family

including C-terminal

resulting in phosphorylation of type I receptors by type II receptors

Binds to cyclins A and E

CD58 Polyclonal Antibody, 100ul[BT-AP02394] Lysosome Defects in EIF2B4 are aThis gene, CYP2A6, 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 protein localizes to the endoplasmic reticulum and its expression is induced by phenobarbital. The enzyme is known to hydroxylate coumarin, and also metabolizes nicotine, aflatoxin B1, nitrosamines, and