Phosphatidylethanolamine N-Methyltransferase (PEMT) Peptide
PEMT
Reactivity: Human
Host: Synthetic
BP, WB
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- Target See all PEMT products
- PEMT (Phosphatidylethanolamine N-Methyltransferase (PEMT))
- Origin
- Human
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB)
- Characteristics
- This is a synthetic peptide designed for use in combination with anti-PEMT antibody (Catalog #: ARP43558_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
- Purification
- Purified
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- Application Notes
- Each Investigator should determine their own optimal working dilution for specific applications.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Concentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Handling Advice
- Avoid repeated freeze-thaw cycles.
- Storage
- -20 °C
- Storage Comment
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Target
- PEMT (Phosphatidylethanolamine N-Methyltransferase (PEMT))
- Synonyms
- zgc:55479 Peptide, DDBDRAFT_0204815 Peptide, DDBDRAFT_0267053 Peptide, DDB_0204815 Peptide, DDB_0267053 Peptide, DDBDRAFT_0219474 Peptide, DDBDRAFT_0267052 Peptide, DDB_0219474 Peptide, DDB_0267052 Peptide, PEAMT Peptide, PEMPT Peptide, PEMT2 Peptide, PNMT Peptide, AI255394 Peptide, Pempt Peptide, Pempt2 Peptide, PHOMETH Peptide, phosphatidylethanolamine N-methyltransferase Peptide, pemt Peptide, MCA3065 Peptide, pmtA Peptide, CNG04250 Peptide, pemtA Peptide, pemtB Peptide, PEMT Peptide, Pemt Peptide
- Background
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PEMT is 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 encodes PEMT protein is within the Smith-Magenis syndrome region on chromosome 17. 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.
Alias Symbols: MGC2483, PEAMT, PEMPT, PEMT2, PNMT
Protein Size: 236 - Molecular Weight
- 26 kDa
- Gene ID
- 10400
- NCBI Accession
- NM_148172, NP_680477
- UniProt
- Q9BW86
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