PEMT Blocking Peptide (N-term)
€363.00
In stock
SKU
AC-BP1025a
Background:
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.
Other Names:
Phosphatidylethanolamine N-methyltransferase, PEAMT, PEMT, PEMT2, PEMT, PEMPT, PNMT
Target/Specificity:
The synthetic peptide sequence is selected from aa 3-17 of HUMAN PEMT
Gene Name: PEMT {ECO:0000255|HAMAP-Rule:MF_03216}
Gene ID: 10400
Primary Accession: Q9UBM1
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
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.
Other Names:
Phosphatidylethanolamine N-methyltransferase, PEAMT, PEMT, PEMT2, PEMT, PEMPT, PNMT
Target/Specificity:
The synthetic peptide sequence is selected from aa 3-17 of HUMAN PEMT
Gene Name: PEMT {ECO:0000255|HAMAP-Rule:MF_03216}
Gene ID: 10400
Primary Accession: Q9UBM1
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
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