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Research reference · 40 mg vial

MOTS-C dosage & reconstitution (40 mg vial)

MOTS-C dosage: calculations for a 40 mg vial use the same amounts described in the literature. Adding 2 mL of bacteriostatic water produces 20 mg/mL, so each U-100 unit contains 200 mcg.

Vial strength 10mg 40mg
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MOTS-C Quick Reference (40 mg vial)

Vial contents40 mg MOTS-C
Final volume2 mL
Concentration20 mg/mL
One U-100 unit200 mcg in 0.01 mL
MOTS-C 40mg

Research context: mechanisms, human and preclinical evidence, limitations and precautions are in How this works and References. The calculator (Spanish) converts any other volume.

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MOTS-C Dosage Chart (40 mg vial)

Dosing & Reconstitution Guide

Educational guide for reconstitution and daily dosing

Standard / Gradual Approach (2 mL = ~20 mg/mL)

Week / phaseDaily doseUnits per injection (mL)
Weeks 1–2200 mcg1 units (0.01 mL)
Weeks 3–4400 mcg2 units (0.02 mL)
Weeks 5–6600 mcg3 units (0.03 mL)
Weeks 7–8800 mcg4 units (0.04 mL)
Weeks 9–10+1 mg (1000 mcg)5 units (0.05 mL)

Frequency: Once daily, subcutaneously, at a consistent time.

Note: For 10-unit or smaller volumes (≤0.10 mL), a 30- or 50-unit syringe reads more accurately.

Reconstitution Steps

  1. Draw 2 mL of bacteriostatic water with a sterile syringe.1
  2. Inject slowly down the vial wall; avoid shaking to prevent foaming.2
  3. Gently swirl or roll until fully dissolved (clear solution).3
  4. Label with the reconstitution date and refrigerate at 2–8 °C, protected from light; use within 4 weeks.4

The per-phase amounts are identical across the MOTS-C family. The 40 mg vial only changes the concentration, U-100 units, volume and supplies.

Important: this guide is for educational purposes only and is not medical advice. For research use only. Not for human consumption.

U-100 Conversion Table (2 mL = 20 mg/mL)

U-100 unitsVolumeContainsYield per vial
20.02 mL400 mcg100 injections
50.05 mL1 mg (1000 mcg)40 injections
100.10 mL2 mg (2000 mcg)20 injections
200.20 mL4 mg (4000 mcg)10 injections
300.30 mL6 mg (6000 mcg)6 injections
500.50 mL10 mg (10000 mcg)4 injections
1001.00 mL20 mg (20000 mcg)2 injections
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Supplies Needed

Straightforward 12- and 24-week planning for a 40 mg vial at 20 mg/mL.

MOTS-C vials (40 mg each)

  • Standard / Gradual Approach, 12 weeks: Minimum 2 vials (56 mg required).
  • Standard / Gradual Approach, 24 weeks: Minimum 4 vials (140 mg required).

U-100 syringes (1 mL)

  • Standard / Gradual Approach, 12 weeks: 84 new syringes for 84 injections.
  • Standard / Gradual Approach, 24 weeks: 168 new syringes for 168 injections.

Bacteriostatic water

  • Standard / Gradual Approach, 12 weeks: 4 mL total (2 mL per vial) → 2 × 3 mL vials.
  • Standard / Gradual Approach, 24 weeks: 8 mL total (2 mL per vial) → 3 × 3 mL vials.

Alcohol swabs

  • Standard / Gradual Approach, 12 weeks: 168 minimum; one box of 100 does not cover the calculation.
  • Standard / Gradual Approach, 24 weeks: 336 minimum; one box of 100 does not cover the calculation.

Sharps container: one appropriately sized. Stability planning: totals are minimum arithmetic quantities; follow the product documentation for sterility, storage, handling loss and discard timing.

MOTS-C 40mgView in store
U-100 syringes (1 mL)1 mL, fine needle
Bacteriostatic water 3 mLView in store
Alcohol swabs70 % isopropyl

Store links may earn a commission. A supplier page is not scientific evidence or proof of suitability for human use.

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MOTS-C Vial and Research Context

  • Reconstitute: add 2 mL of bacteriostatic water to produce 20 mg/mL.
  • Frequency in the source: once daily, subcutaneously.
  • Described range: schedules run from 200 mcg to 1 mg (1000 mcg) per injection.
  • Easy measuring: 1 U-100 unit = 0.01 mL = 200 mcg.
  • Vial size: the 40 mg label is total nominal content, not a per-injection amount.
  • Vial coverage: at 200 mcg per injection one vial supplies 200 injections; at 1 mg (1000 mcg) it supplies 40. These are mass calculations, not storage periods.
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Protocol Overview

Quick reference for the schedules shared by the cited literature.

  • Frequency: once daily.
  • Concentration: 40 mg in 2 mL = 20 mg/mL.
  • Unit conversion: 1 U-100 unit = 200 mcg.
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Dosing Schedule

The tables keep each approach separate.

  • Standard / Gradual Approach: 200 mcg, 400 mcg, 600 mcg, 800 mcg, 1 mg (1000 mcg), in phases (once daily).
  • Measurement: use the units and mL shown beside each amount.
  • Consistency: vial size does not change the schedule.
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Storage Instructions

  • Lyophilized (unopened): −20 °C for long-term storage; 2–8 °C if used within weeks. Protected from light.
  • Reconstituted: 2–8 °C, do not freeze. Use within the documented period (typically up to 4 weeks with bacteriostatic water).
  • Handling: do not shake; avoid temperature cycling; label with date and concentration.
  • Discard: cloudy solutions, particulates or expired preparations are discarded.

More detail in the storage guide (Spanish).

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Important Notes

  • Research only: the referenced compounds are sold for laboratory research. Nothing here is medical advice or an administration schedule.
  • Above 100 units: a 1 mL U-100 syringe cannot hold them; split across syringes or reconstitute with less volume.
  • Accuracy: concentration depends on the actual volume added; measure the diluent with a syringe, not by eye.
  • Verification: confirm vial contents against the batch certificate of analysis before calculating.
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How This Works

MOTS-C exerts its effects through multiple metabolic signaling pathways:

AMPK Activation:

The peptide directly activates AMPK (AMP-activated protein kinase), the cell's master energy sensor. AMPK activation triggers cascades that favor fatty acid oxidation, improve insulin-independent glucose uptake, and increase mitochondrial biogenesis.

Folate pathway regulation:

Modulates folate metabolism and the methionine cycle, impacting DNA methylation and epigenetic regulation associated with cellular aging.

Nuclear translocation under stress:

Under metabolic stress conditions (fasting, exercise, caloric restriction), MOTS-C translocates from the mitochondria to the nucleus, where it modulates the expression of adaptive genes as an integrated stress response.

Improvement of mitochondrial function:

Increases electron transport chain activity, improves coupling between oxidative phosphorylation and ATP production, and reduces mitochondrial reactive oxygen species (ROS) generation.

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Research Applications

Active research lines with MOTS-C documented in the scientific literature:

  • Resistencia a la insulina: studies in murine models describe a 30 to 50% improvement in insulin sensitivity with chronic treatment
  • Obesidad inducida por dieta: protection against weight gain in high-fat diet models
  • Capacidad aeróbica y ejercicio: increased muscle oxidative capacity in preclinical models, a phenomenon described as “exercise in an injection” in the literature
  • Envejecimiento metabólico: endogenous levels decline with age, which correlates with metabolic decline in the studies
  • Fatty liver disease Reduced hepatic lipid content in NAFLD models
  • Cardioprotección: effects on myocardial ischaemia-reperfusion in models
  • Neuroprotection investigaciones preliminares sobre Parkinson y enfermedad de Alzheimer
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Precautions Described in the Literature

MOTS-C is an endogenous peptide, and the preclinical literature and first published trials describe a notably clean tolerability profile. In the experimental context, the literature mainly documents:

  • Reacciones locales leves y transitorias descritas en los estudios
  • Cefalea ocasional reportada en fases tempranas
  • Mild hypoglycaemia described in models with advanced insulin resistance

Given its mechanism of improving insulin sensitivity, the literature notes potential interactions with antidiabetic agents (sulfonylureas, insulin, metformin) as a variable to control for in experimental design. Always handle under appropriate laboratory practice.

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Injection Technique in Research

  • Route in the studies: subcutaneous, in abdominal or thigh adipose tissue, rotating the site.
  • Syringe: 1 mL U-100 (100 units); read in units, not mL.
  • Asepsis: alcohol swab on the stopper and the site; a new syringe per injection.
  • Drawing: purge air, draw the units from the chart and verify before withdrawing the needle from the vial.

Full guide: U-100 syringes and reading units (Spanish).

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Research Note

All content on this page is technical and educational. It describes how a vial is reconstituted, how a syringe is read and which amounts the cited sources describe. It does not replace the supervision of a qualified researcher or the judgment of a health professional, and it is not intended to diagnose, treat, cure or prevent any disease.

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References

  1. Lee C, Zeng J, Drew BG, et al. The mitochondrial-derived peptide MOTS-c promotes metabolic homeostasis and reduces obesity and insulin resistance. Cell Metab. 2015;21(3):443-454.
  2. Reynolds JC, Lai RW, Woodhead JST, et al. MOTS-c is an exercise-induced mitochondrial-encoded regulator of age-dependent physical decline and muscle homeostasis. Nat Commun. 2021;12:470.
  3. Kim KH, Son JM, Benayoun BA, Lee C. The mitochondrial-encoded peptide MOTS-c translocates to the nucleus to regulate nuclear gene expression. Cell Metab. 2018;28(3):516-524.
  4. Yang Y, Gao H, Zhou H, et al. The role of mitochondrial-derived peptide MOTS-c in metabolic homeostasis. Pharmacol Res. 2019;143:166-171.
  5. Merry TL, Chan A, Woodhead JST, et al. Mitochondrial-derived peptides in energy metabolism. Am J Physiol Endocrinol Metab. 2020;319(4):E659-E666.
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Related Protocols

Research material only. Technical and educational content. Not medical advice, an administration schedule or a recommendation for use, and not intended to diagnose, treat, cure or prevent any disease. The referenced compounds are sold for laboratory research.

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