Research use only.  Educational reference. Not medical advice. Not for human consumption.
⚙️ Mitochondrial-Derived Peptide

MOTS-c Dosage Protocols: All Vial Sizes

MOTS-c is a 16-amino-acid peptide encoded within the mitochondrial 12S rRNA gene. It functions as an exercise mimetic and metabolic regulator; circulating levels decline with aging and obesity. Choose your vial size below; each size has its own exact dosing table.

Choose Your Vial Size

VialFinal volumeConcentrationOne U-100 unit
10 mg3 mL3.33 mg/mL33.33 mcg in 0.01 mLOpen protocol →
40 mg3 mL13.33 mg/mL133.33 mcg in 0.01 mLOpen protocol →
motsc-40mg-4ml4 mL10 mg/mL100 mcg in 0.01 mLOpen protocol →

Doses are the same research amounts across sizes; the vial size changes the concentration, so syringe units differ. Always use the table for your exact vial.

Storage Instructions

StateTemperatureDuration
Lyophilized−20°C (−4°F)Up to 24 months, dry & dark
Reconstituted2–8°C (35–46°F)Up to 7 days, protect from light

Important Notes

⚠ Research Use Only: MOTS-c is investigational. Most evidence from rodent studies; human clinical trials are early-stage.

How This Works

MOTS-c is encoded within the mitochondrial 12S rRNA gene — one of the few human peptides with mitochondrial DNA origin. Under metabolic stress it translocates from mitochondria to the nucleus, regulating gene expression alongside AMPK signaling.

Effects include AMPK activation, upregulation of fatty-acid oxidation, mitochondrial biogenesis, and improved insulin-stimulated glucose uptake. In animal models it produces exercise-mimetic effects: improved running endurance, glucose disposal, and reduced adiposity on high-fat diet.

Potential Benefits & Side Effects

Potential Benefits

Side Effect Profile

Lifestyle Factors

Injection Technique

References

1
Lee C et al. 'MOTS-c promotes metabolic homeostasis' — Cell Metab, 2015 View source ↗
2
Reynolds JC et al. 'MOTS-c regulator of age-dependent decline' — Nat Commun, 2021 View source ↗
3
Kim KH et al. 'MOTS-c regulates nuclear gene expression' — Cell Metab, 2018 View source ↗