53-84-9
Most orderedNAD+
The oxidised pyridine dinucleotide cofactor, supplied lyophilised for redox, sirtuin and PARP work. Released at ≥ 98.0% by HPLC.
From
£42.00
In stock
Mitochondrial ORF of the 12S rRNA type-c · MOTSc · MOTS-c peptide
A 16-residue mitochondrial-derived peptide encoded in mtDNA. Supplied lyophilised, released at ≥ 99.0% by RP-HPLC.
Total, ex VAT
£86.00
For laboratory research use only. Not for human or veterinary use, and not a medicine, food or cosmetic. Sold to qualified researchers and institutions who accept responsibility for safe handling and lawful use.
Compound data
Indicative values for this line. The certificate issued with your batch is the authoritative record and reports the measured figures for the material you receive.
Targets and pathways
Overview
MOTS-c is a 16-residue peptide encoded not in the nuclear genome but within the mitochondrial 12S ribosomal RNA gene — one of a small set of mitochondrial-derived peptides that upended the assumption that mtDNA encodes only respiratory-chain subunits and RNA machinery. Its identification in 2015 gave the field a concrete molecule for studying how mitochondria signal outward to the rest of the cell.
Mechanistically it is studied as a regulator of the folate-methionine one-carbon cycle. Interference with that cycle causes AICAR to accumulate, and AICAR is an endogenous AMPK activator — which places MOTS-c upstream of a metabolic sensor rather than acting directly on it. Under metabolic stress the peptide has also been shown to translocate to the nucleus and associate with stress-responsive transcription factors, making it a working example of retrograde mitonuclear communication.
Two methionine residues sit in the sequence, and both are oxidation-prone. Methionine sulfoxide formation is the single most common reason a MOTS-c preparation drifts off specification, and it appears on RP-HPLC as a new peak eluting slightly ahead of the parent. Ryzen holds material under inert atmosphere and releases against a ≥ 99.0% area-percent specification with the oxidised species reported separately where detected.
In short
Where it is used
MOTS-c is the standard tool for studying retrograde communication — how mitochondrial state is reported to nuclear transcription — because it is a discrete, synthesisable molecule rather than a diffuse metabolic signal.
Work on the folate–methionine cycle uses MOTS-c to perturb purine biosynthesis and observe the downstream AICAR accumulation that follows, linking a mitochondrial peptide to a nuclear-encoded metabolic sensor.
Endogenous MOTS-c rises with exercise in several models, and the peptide is used in studies of substrate utilisation, glucose uptake and physical performance in muscle preparations.
The peptide is used in diet-induced insulin resistance models to characterise the relationship between mitochondrial signalling and peripheral glucose handling.
Circulating MOTS-c declines with age in several species, and the peptide appears frequently in work on mitochondrial contributions to cellular ageing.
Handling
Add diluent slowly against the vial wall and allow the powder to go into solution unaided. MOTS-c dissolves quickly and does not need warming. Minimise headspace and time-in-air once open: the methionine residues oxidise on exposure, and each opening of a working vial costs measurable purity.
Lyophilised and stored at −20 °C, desiccated and dark, material is stable for at least 24 months. In solution at 2–8 °C, use within 14 days — shorter than most peptides in the catalogue, because of the oxidation risk. Aliquot at first reconstitution rather than drawing repeatedly from one vial.
Laboratory reference
Enter the fill weight on the vial and the diluent volume you intend to add. The calculator returns the resulting solution concentration and the volume that contains a given mass.
Figures are mass-to-volume arithmetic for laboratory preparation of MOTS-c and take no account of net peptide content, which is stated on the batch certificate and should be applied to the fill weight before calculating. Nothing here constitutes dosing, administration or clinical guidance of any kind.
Published work
Summaries of published findings, provided as research reference. These describe work done by others in preclinical and clinical settings; they are not claims about this material or outcomes for any reader.
The founding paper identified MOTS-c as a peptide encoded in the mitochondrial 12S rRNA region, showed it regulates the folate–methionine cycle with downstream AICAR accumulation and AMPK activation, and reported improved insulin sensitivity in diet-induced obese mice.
Lee et al., Cell Metabolism, 2015
Metabolic stress was shown to drive MOTS-c into the nucleus, where it associates with stress-responsive transcription factors and regulates a set of nuclear genes with antioxidant response elements — direct evidence of mitonuclear retrograde signalling.
Kim et al., Cell Metabolism, 2018
Treatment in mice was associated with improved physical performance across young, middle-aged and old cohorts, and with changes in skeletal muscle gene expression consistent with an exercise-associated programme.
Reynolds et al., Nature Communications, 2021
Several groups have reported that circulating MOTS-c falls with age and varies with metabolic status, which underpins its use as a candidate biomarker as well as a research tool.
Multiple cohorts, reviewed in Kim & Lee, Trends in Endocrinology & Metabolism
Questions
Something not covered here? Ask us directly — technical questions reach someone who runs the assays.
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Important
MOTS-c is supplied strictly for laboratory research and analytical use. It is not a medicine, food, cosmetic or veterinary product; it is not for human or animal consumption; and it is not intended to diagnose, treat, cure or prevent any condition. It is not manufactured, tested or released to any standard that would support administration to humans or animals. Information on this page is compiled for research reference and is not medical advice. No dosing, administration or therapeutic guidance is given or implied. By ordering you confirm you are a qualified researcher or institution and accept responsibility for safe handling and lawful use.