NAD+ 500 mg (β-Nicotinamide adenine dinucleotide; Nadide) from Peptide Tech is a premium, lyophilized research-use-only (RUO) reagent supplied at ≥99% purity (HPLC & MS verified). The oxidized dinucleotide cofactor is widely used in in-vitro redox biochemistry, enzyme kinetics, ADP-ribosylation workflows, and LC–MS metabolomics where identity, stability, and batch traceability are critical.
Specifications
| Property | Details |
|---|---|
| CAS Number | 53-84-9 |
| Chemical Name | β-Nicotinamide adenine dinucleotide (oxidized form); NAD+; Nadide |
| PubChem CID | 5892 |
| Molecular Formula | C21H27N7O14P2 |
| Molecular Weight | ≈ 663.43 g/mol |
| Physical Appearance | White to off-white lyophilized powder |
| Form | Oxidized dinucleotide cofactor (anhydrous) |
| Container | Glass vial (500 mg net content) |
| Purity | ≥99% verified by HPLC & MS (batch COA via on-vial QR) |
| Solubility | Readily soluble in sterile water and compatible neutral buffers; prepare fresh, protect from light, avoid alkaline pH. |
| Intended Use | Laboratory research only (RUO). Not for human or animal use. |
Molecular Structure
Key Features of Peptide Tech
- Same-Day Shipping (Mon–Fri, on in-stock items)
- GMP-Aligned lyophilized reagents
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- Batch Tracking with QR Code Verification
- 3rd-Party U.S. Lab Testing — purity, quantity, endotoxin
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Potential Applications in Research
Strictly in-vitro, cell-free, or cell-based workflows. No health claims or clinical/veterinary use.
- Oxidoreductase enzyme kinetics (e.g., LDH, MDH, ADH) monitoring NADH formation at 340 nm or via fluorescence to determine Vmax/Km and inhibitor effects.
- Sirtuin deacetylase assays that consume NAD+ to generate OAADPr and nicotinamide, quantified by LC–MS or homogeneous fluorescence kits.
- PARP/ARTD ADP-ribosylation workflows (auto- and trans-modification) with immuno or LC–MS readouts to map poly/mono-(ADP-ribose) formation.
- NAD+-dependent DNA ligase assays (LigA) for nick-sealing efficiency, cofactor dependence, and inhibitor screening.
- Metabolomics method development (LC–MS/MS) for redox-pair profiling of NAD+/NADH and NADP(H) in buffered matrices.
- Assay calibration & stability studies (RP-HPLC/LC–MS) establishing retention, ionization, and recovery of dinucleotides.
Quality, Storage & Handling
Each lot is confirmed by HPLC (purity) and MS (identity); COA and batch data are accessible via QR. Independent U.S. labs verify purity, quantity, and endotoxin.
- Storage (lyophilized): −20 °C long-term or 2–8 °C short-term; keep desiccated and protected from light.
- After reconstitution: Use neutral, oxygen-poor buffer when possible; aliquot and store at ≤−20 °C; avoid repeated freeze–thaw.
- Working solutions: Prepare fresh; minimize exposure to light and high pH to reduce degradation.
Shipping & Fulfillment
Ships with validated cold-chain packaging. In-stock orders placed before the daily cutoff ship the same day. 2-Day FedEx/UPS is standard, with overnight options available. Automated text/email updates included; international shipping available where permitted.
Compliance & RUO Disclaimer
For laboratory research only. Not a drug, cosmetic, food, or household chemical. Not for human or animal use, ingestion, diagnostic, or therapeutic applications. Buyers warrant they are qualified to handle RUO materials under applicable laws and institutional guidelines.
FAQs
- Is this the oxidized form?
- Yes. This product is NAD+ (oxidized). For reduced NADH or NADP(H), see our catalog.
- What purity is provided?
- Each 500 mg vial is ≥99% by HPLC with MS identity confirmation; third-party testing is performed on every lot (COA via QR).
- How should I reconstitute it?
- Use sterile water or a neutral, compatible buffer; gently invert to dissolve. Prepare fresh working solutions, aliquot, and avoid alkaline pH and repeated freeze–thaw.
- Which in-vitro assays is NAD+ commonly used in?
- Typical RUO uses include dehydrogenase kinetics (340 nm), sirtuin and PARP assays, NAD+-dependent ligase reactions, and LC–MS method development for dinucleotides.
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