Third-Party Tested ≥98% HPLC Purity — USA Shipped

Weight Management Research Guide

MOTS-C: Dosage, Benefits & Research Guide

Also known as: Mitochondrial ORF of the 12S rRNA type-c, MOTSc

Key Facts

MOTS-C is a weight management research peptide (C101H152N28O22S2, MW 2174.64 g/mol). Mitochondrial-derived peptide for metabolic regulation and cellular energy research. It is supplied as a lyophilized powder for laboratory and in-vitro research use only — not for human consumption.

Classification Mitochondrial-derived peptide
Molecular Formula C101H152N28O22S2
Molecular Weight 2174.64 g/mol
CAS Number 1627580-64-6
Research Half-Life Short circulating half-life in preclinical models
Form Lyophilized powder
Research Category Weight Management

What is MOTS-C?

MOTS-c (Mitochondrial Open Reading Frame of the Twelve S rRNA type-c) is a 16-amino acid peptide encoded within the mitochondrial genome, specifically within the 12S rRNA gene. Its primary mechanism of action involves activation of the AMPK pathway, which regulates cellular energy homeostasis by promoting glucose uptake and fatty acid oxidation independent of insulin signaling. Research published by Lee et al. (Cell Metabolism, 2015) demonstrated that MOTS-c administration in diet-induced obese mice significantly improved glucose tolerance and reduced fat accumulation without altering food intake. Subsequent studies from the same USC laboratory showed that MOTS-c levels decline with age in human plasma, and that exercise increases circulating MOTS-c levels, suggesting it functions as a mitochondrial-derived exercise mimetic. Unlike traditional metabolic peptides that target specific membrane receptors, MOTS-c is unique in that it translocates to the nucleus under metabolic stress to regulate nuclear gene expression, particularly genes involved in the methionine-folate cycle and de novo purine biosynthesis. Compared to other mitochondrial-derived peptides like humanin, MOTS-c appears more specifically involved in metabolic regulation rather than cytoprotection. The lyophilized peptide should be stored at -20C and protected from light; reconstitute with bacteriostatic water and store reconstituted solutions at 2-8C for up to 21 days. MOTS-c is primarily researched by aging biology laboratories, exercise physiology departments, and mitochondrial medicine research centers investigating metabolic signaling peptides.

MOTS-C Research Applications

In published and preclinical research, MOTS-C has been studied across the following areas:

  • Glucose regulation and insulin sensitivity
  • Skeletal muscle energy and endurance
  • Fat oxidation and adipose tissue studies
  • Longevity and age-related health research

MOTS-C in Research: Reconstitution & Study Concentrations

MOTS-c is a 16-amino-acid mitochondrial-derived peptide studied for its role in metabolic homeostasis, insulin sensitivity and exercise-mimetic signaling via AMPK. Research concentrations are model-specific. The lyophilized peptide is reconstituted with bacteriostatic water for laboratory use only.

Worked example: a 10mg vial reconstituted with 2 mL of bacteriostatic water yields 5.00 mg/mL.

Open the reconstitution calculator

MOTS-C — Frequently Asked Questions

What is MOTS-C and how does it work?
MOTS-C is a mitochondrial-derived peptide (MDP) encoded by the 12S rRNA gene within mitochondrial DNA. It is a 16-amino acid peptide that has been observed to activate AMPK (AMP-activated protein kinase) signaling, which plays a central role in cellular energy homeostasis. In preclinical models, MOTS-C translocates to the nucleus under metabolic stress and regulates gene expression related to glucose metabolism and fatty acid oxidation.
What research has been done on MOTS-C?
Research published by Dr. Changhan David Lee's lab at USC (Cell Metabolism, 2015) first identified MOTS-C as a mitochondrial-encoded signaling peptide. Subsequent studies demonstrated that MOTS-C administration improved glucose regulation in diet-induced obesity mouse models. Additional published research has examined its role in skeletal muscle metabolism during exercise, age-related metabolic decline, and insulin sensitivity in high-fat diet models.
How does MOTS-C compare to Humanin?
Both MOTS-C and Humanin are mitochondrial-derived peptides (MDPs), but they have distinct mechanisms. Humanin primarily acts through cytoprotective and anti-apoptotic pathways via STAT3 signaling, while MOTS-C activates AMPK to regulate metabolic homeostasis. MOTS-C is a shorter peptide (16 amino acids vs. 24 for Humanin) and has been more extensively studied for its effects on glucose metabolism and exercise physiology.
What is the recommended reconstitution protocol for MOTS-C?
For this 10mg vial, add 2 mL of bacteriostatic water to yield a concentration of 5.0mg/mL. Draw 20 units on a 1mL insulin syringe for a 1 mg dose. Inject BAC water slowly along the inner vial wall — do not shake. Allow the powder to dissolve fully (2–5 minutes). Administer in the AM. Use 5 days on, 2 days off. Refrigerate reconstituted solution at 2–8°C and use within 30 days.
Is MOTS-C legal to buy for research?
MOTS-C is sold in the United States as a research chemical for laboratory and in-vitro use only. It is not approved by the FDA for human use and is not sold for human consumption. Researchers are responsible for compliance with all applicable federal, state, and institutional regulations.
How is MOTS-C reconstituted for research use?
MOTS-C ships as a lyophilized (freeze-dried) powder and is reconstituted with bacteriostatic or sterile water before use in research. The volume of solvent added determines the working concentration — use the Elyte reconstitution calculator to derive the exact concentration for a given vial size and solvent volume.
Does MOTS-C come with a Certificate of Analysis?
Yes. Every batch of MOTS-C from Elyte Peptides ships with a third-party Certificate of Analysis (COA) documenting identity and HPLC purity (≥98%), so research results can be traced to a verified lot.

Research References

  1. Lee C et al. The mitochondrial-derived peptide MOTS-c promotes metabolic homeostasis. Cell Metab 2015.