NAT6 Antibody (Center) Blocking Peptide
Synthetic peptide
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Primary Accession | Q93015 |
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Clone Names | 100603269 |
Gene ID | 24142 |
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Other Names | N-acetyltransferase 6, 231-, Protein fusion-2, Protein fus-2, NAT6, FUS2 |
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 | NAA80 {ECO:0000303|PubMed:29581253, ECO:0000312|HGNC:HGNC:30252} |
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Function | N-alpha-acetyltransferase that specifically mediates the acetylation of the acidic amino terminus of processed forms of beta- and gamma-actin (ACTB and ACTG, respectively) (PubMed:30028079, PubMed:29581253). N-terminal acetylation of processed beta- and gamma- actin regulates actin filament depolymerization and elongation (PubMed:29581253). In vivo, preferentially displays N-terminal acetyltransferase activity towards acid N-terminal sequences starting with Asp-Asp-Asp and Glu-Glu-Glu (PubMed:30028079, PubMed:29581253). In vitro, shows high activity towards Met-Asp-Glu-Leu and Met-Asp-Asp-Asp (PubMed:10644992, PubMed:29581307). May act as a tumor suppressor (PubMed:10644992). |
Cellular Location | Cytoplasm, cytosol |
Tissue Location | Strongly expressed in heart and skeletal muscle, followed by brain and pancreas, with weak expression in kidney, liver, and lung and no expression in placenta. |
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Provided below are standard protocols that you may find useful for product applications.
Background
NAT6 seems to be involved in N-acetylation. Acts on peptides with a N-terminal Met followed by Asp/Glu/Asn. May act as a tumor suppressor.
References
Young, R.P., et al. Postgrad Med J 85(1008):515-524(2009)Muzny, D.M., et al. Nature 440(7088):1194-1198(2006)Duh, F.M., et al. Mol. Cell. Probes 18(1):39-44(2004)Shuttleworth, T.L., et al. J. Biol. Chem. 277(25):23008-23018(2002)Lerman, M.I., et al. Cancer Res. 60(21):6116-6133(2000)
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