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NAD+

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  • 1.Aging & Longevity:
  •  NAD+ levels decline with age in multiple tissues.
  • Supplementation with precursors (e.g., NR, NMN) restores NAD-and has been shown in preclinical models to improve mitochondrialfunction,enhance DNA repair, and extend lifespan in lower organisms.
  • 2. Neurodegeneration
  • Depletion of NAD+ is linked to neurodegenerative diseases (e.g., Alzheimer's, Parkinson's).
  • NAD- boosting strategies have shown neuroprotective effects in animal models, reducing neuroinflammation and improving cognitiveperformance. 
  • 3.Metabolic Disorders 
  • NAD+ plays a crucial role in insulin sensitivity, lipid metabolism, and mitochondrial biogenesis.
  • Restoring NAD- levels improves metabolic health in models of obesity, diabetes, and fatty liver disease.
  • 4.DNA Repair & Cancer 
  • PARP-mediated DNA repair consumes NAD+.
  •  Cancer cells often upregulate NAD+ biosynthesis to sustain growth.
  • Therapeutic strategies include PARP inhibitors and NAMPT inhibitors for targeting cancer metabolism. 
  • 5.Immune Function & Inflammation 
  •  CD38, an NAD+-consuming enzyme, is upregulated in aging and chronic inflammation.
  •  Modulating NAD+ metabolism influences immune cell activation and cytokine production. 
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  • NAD+
  • NAD+
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  • NAD+
  • Description
NAD+ (nicotinamide adenine dinucleotide)is a critical coenzymenaturally present in all living cells and has been the subject ofextensive biochemical and molecular research for decades. It plays anessential role in fundamental cellular processes, particularly thoserelated to energy metabolism, redox signaling, genomic maintenance,and cellular homeostasis. Due to its central role in cellular function,NAD+ is widely studied in academic, clinical, and laboratory researchenvironments focused on metabolic regulation, cellular agingmechanisms, and stress-response pathways.
At the molecular level, NAD+ functions as an electron carrier, cyclingbetween its oxidized form (NAD+) and its reduced form (NADH). Thisreversible conversion enables NAD+ to participate in redox reactionsthat are foundational to metabolic balance within experimental systems.These reactions support core biochemical pathways investigated inresearch models, including glycolysis, the tricarboxylic acid (TCA)cycle, and oxidative phosphorylation.
NAD+ is recognized in research literature as a cornerstone moleculedue to its involvement in hundreds of enzymatic reactions acrossnearly every major metabolic pathway studied in biological systems.Experimental data consistently demonstrate that reduced intracellularNAD+ availability in research models is associated with impairedenergy transfer, altered signaling cascades, and diminished capacityfor maintaining cellular and genomic integrity.
In laboratory settings, NAD+ is also studied for its role as a substratefor enzymes such as sirtuins, PARPs, and CD38, all of which are centralto research into DNA repair mechanisms,epigenetic regulation, andcellular stress responses. These investigations are conducted usingcontrolled in vitro and in vivo research models to better understandmolecular behavior, pathway interactions, and biochemical regulation.
For experimental consistency and analytical accuracy, research-gradeNAD+ materials are typically characterized by high purity,manufactured under controlled conditions, and verified as LPS-freepeptide, endotoxin-free peptide, and research peptides endotoxintested,ensuring minimal interference with sensitive cellular andbiochemical assays. These quality parameters are essential formaintaining reproducibility and validity in advanced laboratoryresearch.
This material is intended strictly for research purposes only. Not forhuman or animal use.
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