This gene encodes an enzyme which converts phosphatidylethanolamine to phosphatidylcholine by sequential methylation in the liver. The protein localizes to the endoplasmic reticulum and mitochondria-associated membranes. The gene is within the Smith-Magenis syndrome region on chromosome 17. Alternate splicing of this gene results in three transcript variants encoding two different isoforms.
PEAMT; PEMT; PEMT2; Phosphatidylethanolamine N-methyltransferase; Phosphatidylethanolamine N-methyltransferase MGC2483 PEAMT PEMPT PEMT2 PNMT; phosphatidylethanolamine N-methyltransferase-like protein; Phospholipid methyltransferase; PLMT
Cat # 15595422
100 µL
Cat # 16145012
50 µg
Cat # 15717811
100 µL
Cat # 16550872
100 µg
Cat # 16044357
400 uL
Cat # 15784586
100 ul
Cat # 16162446
100 µg
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