PEMT antibody (C-Term)
Quick Overview for PEMT antibody (C-Term) (ABIN2781316)
Target
See all PEMT AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- C-Term
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Purpose
- PEMT Antibody - C-terminal region
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Sequence
- GWAIMHASPT GLLLTVLVAL TYIVALLYEE PFTAEIYRQK ASGSHKRS
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Predicted Reactivity
- Cow: 93%, Dog: 86%, Guinea Pig: 83%, Horse: 100%, Human: 100%, Mouse: 100%, Pig: 86%, Rabbit: 100%, Rat: 100%, Yeast: 100%, Zebrafish: 82%
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Characteristics
- This is a rabbit polyclonal antibody against PEMT. It was validated on Western Blot using a cell lysate as a positive control.
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Purification
- Affinity Purified
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Immunogen
- The immunogen is a synthetic peptide directed towards the C terminal region of human PEMT
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Application Notes
- Optimal working dilution should be determined by the investigator.
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Comment
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We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP43558-100UG
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 0.5 mg/mL
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Buffer
- Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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Preservative
- Sodium azide
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Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Handling Advice
- prevent freeze-thaw cycles
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Storage
- 4 °C,-20 °C
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Storage Comment
- For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.
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- PEMT (Phosphatidylethanolamine N-Methyltransferase (PEMT))
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Alternative Name
- PEMT
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Background
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Background Information: 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.
Gene Name: Phosphatidylethanolamine N-methyltransferase
Alternative Symbols: PLMT, PNMT, PEAMT, PEMPT, PEMT2
Protein Name: Phosphatidylethanolamine N-methyltransferase
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Molecular Weight
- 22 kDa
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Gene ID
- 10400
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NCBI Accession
- NP_680477
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UniProt
- Q9BW86
Target
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