🇬🇧 UK Manufactured & TestedCertificate of Analysis IncludedFor Research Use Only
Mercia Research
NAD+ — Mercia Research peptide

Lot 24-8501

NAD+ · 1000mg

≥99.0%

Research applications

  • Sirtuin pathway research
  • Mitochondrial electron transport
  • Longevity / cellular bioenergetics
For laboratory research use only. Not intended for human or animal consumption. Mercia Research supplies these compounds for in vitro research and analytical work by qualified personnel.

Sequence

C₂₁H₂₇N₇O₁₄P₂

Molecular weight

663.43 g/mol

Purity

≥99.0%

Abbreviation

NAD

Storage

Lyophilized: −20 °C, protected from light. Reconstituted: 2–8 °C, 7 days.

Reconstitution

Add 5 mL BAC water to a 1000 mg vial → 200 mg/mL.

⚠ For laboratory research use only — not for human or animal consumption

NAD+

Nicotinamide adenine dinucleotide.

4.7 (281)

A central cellular cofactor for redox reactions and sirtuin/PARP activity. Researched in cellular bioenergetics, sirtuin signalling, and longevity models.

Configure

£72.00

Vial size

Lot 24-8501 · lot-matched COA included · cold-chain shipping

Qty

1
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Research Overview

NAD+ (Nicotinamide Adenine Dinucleotide) is a central coenzyme found in all living cells. It plays a fundamental role in cellular energy metabolism and serves as a substrate for several classes of regulatory enzymes. Its decline with age has made it a major focus of longevity and metabolic research.

Sirtuin Pathway Research

NAD+ is an obligatory substrate for the sirtuin family of NAD+-dependent deacylases (SIRT1–7). Research has examined NAD+'s role in regulating sirtuin enzymatic activity, sirtuin-mediated histone deacetylation and gene expression changes, and the relationship between cellular NAD+ levels and sirtuin-dependent metabolic regulation.

PARP Activity and DNA Repair

Poly(ADP-ribose) polymerases (PARPs) consume NAD+ during DNA damage repair. Research has investigated the competition between PARP activity and sirtuin function for cellular NAD+ pools, NAD+ depletion as a consequence of DNA damage-induced PARP hyperactivation, and strategies to maintain NAD+ availability in models of genotoxic stress.

Mitochondrial Electron Transport

NAD+ and its reduced form NADH are central to mitochondrial oxidative phosphorylation. Research has examined NAD+/NADH ratio dynamics in mitochondrial function, the role of complex I in NADH oxidation and ATP generation, and mitochondrial NAD+ pools as distinct from cytosolic pools in cellular energy models.

Longevity and Cellular Bioenergetics

The decline of cellular NAD+ with age has positioned it as a key subject in longevity research, including studies of NAD+ precursor supplementation effects, the relationship between NAD+ levels and age-related metabolic dysfunction, and interactions with other longevity-associated pathways including AMPK and mTOR.

For laboratory research use only. Not intended for human or animal consumption.