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Approximately 100 ng of the DNA fragment was incubated with the purified protein in a reaction mixture containing 1X binding buffer (15 mM HEPES, pH 7.5, 35 mM KCl, 1 mM MgCl2, 1 mM EDTA, pH 8.0, 2% glycerol, and 1 mM DTT) in a total volume of 20 l

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Quality & Verification 99% purity confirmed via LC-MS/MS Endotoxin-tested for laboratory suitability Independently verified Certificate of Analysis Tested in the USA Scientific Literature & Research ContextResearch involving NNMT inhibition highlights its role in metabolic regulation, NAD metabolism, and epigenetic signaling pathways: Kraus, D

doi: 10.1080/09546634.2017.1392476 [DOI] [PubMed] [Google Scholar] 85.Tehranchinia Z, Saghi B, Rahimi H

Diabetes 58, 23032315