HRASLS5 Antibody (Center) Blocking peptide
Synthetic peptide
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Primary Accession | Q96KN8 |
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Clone Names | 91230015 |
Gene ID | 117245 |
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Other Names | Ca(2+)-independent N-acyltransferase, iNAT, 231-, H-rev107-like protein 5, HRAS-like suppressor 5, HRSL5, HRASLS5, HRLP5 |
Target/Specificity | The synthetic peptide sequence used to generate the antibody AP13881c was selected from the Center region of HRASLS5. A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay. |
Format | Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed. |
Storage | Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C. |
Precautions | This product is for research use only. Not for use in diagnostic or therapeutic procedures. |
Name | PLAAT5 (HGNC:24978) |
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Synonyms | HRASLS5, HRLP5 |
Function | Exhibits both phospholipase A1/2 and acyltransferase activities (PubMed:22825852, PubMed:26503625). Shows phospholipase A1 (PLA1) and A2 (PLA2) activity, catalyzing the calcium-independent release of fatty acids from the sn-1 or sn-2 position of glycerophospholipids (PubMed:22825852). Shows N-acyltransferase activity, catalyzing the calcium-independent transfer of a fatty acyl group at the sn-1 position of phosphatidylcholine (PC) and other glycerophospholipids to the primary amine of phosphatidylethanolamine (PE), forming N-acylphosphatidylethanolamine (NAPE), which serves as precursor for N-acylethanolamines (NAEs) (PubMed:19000777, PubMed:22825852). |
Cellular Location | Cytoplasm, cytosol {ECO:0000250|UniProtKB:Q4KLN5} |
Tissue Location | Highest expression level in testis and pancreas. |
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Provided below are standard protocols that you may find useful for product applications.
References
Jin, X.H., et al. Biochim. Biophys. Acta 1791(1):32-38(2009)Lamesch, P., et al. Genomics 89(3):307-315(2007)Jin, X.H., et al. J. Biol. Chem. 282(6):3614-3623(2007)
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