MID-35 for Muscle Growth - Quick Reference Sheet

MID-35 for Muscle Growth

Created on 09/13/2026 – Quick Reference based on Evidence Review created using AI4L / Opus 5 Audit

MID-35 is a laboratory-made protein fragment built to block the body's own brake on muscle growth. One injection kept mouse muscle larger for months. Every finding comes from mice, from the laboratory that invented the compound. No person has ever received it, no approved source exists, and no human dose is known. (Full Review)

Protocol

No human protocol exists
Laboratory regimens only
No clinic, practitioner or guideline uses MID-35, and no conversion to a human dose has been attempted.
Direct intramuscular regimen
30 nmol once, in mice
One injection into the shin muscle of young mice; 2 nmol sufficed in adult mice.
Transdermal iontophoresis regimen
Needle-free alternative
Weak electrical current drives the peptide through skin into the underlying muscle.
Time to effect
Peak muscle gain
~28 days
In mice, muscle weight gain peaked around 28 days.
Persistence of effect
12 weeks
In mice, the gain from a single dose persisted 12 weeks.
First measurable gain
14 days
In mice, gene-level changes appeared within 3 days but measurable muscle weight gain took 14 days.

Benefits

Contraindications
  • Anyone outside a formal research setting
  • Active or recently treated malignancy (within 5 years)
  • Pregnancy and lactation
  • Bleeding disorders, or anticoagulation with an international normalized ratio above 3.0
  • Hereditary hemorrhagic telangiectasia or any known vascular malformation syndrome
  • Severe kidney impairment (estimated glomerular filtration rate below 30 mL/min/1.73 m²)
  • Known tendon pathology, or recent tendon rupture or repair (within 12 months)
Key Interactions
  • Anticoagulants and antiplatelets (warfarin, apixaban, rivaroxaban, clopidogrel): caution
  • NSAIDs (non-steroidal anti-inflammatory drugs; ibuprofen, naproxen, high-dose aspirin): caution
  • Glucocorticoids (prednisone, dexamethasone): monitor
  • GLP-1 receptor agonists (semaglutide, tirzepatide): monitor
  • Androgens and selective androgen receptor modulators (testosterone, enobosarm): caution
  • Supplements with additive or overlapping action (creatine monohydrate, HMB, leucine-rich essential amino acids, epicatechin, follistatin-containing egg-yolk extracts): caution
  • Other interventions (resistance training, blood-flow-restriction training): caution

Risk & Side Effects

  • High:
  • Medium:
  • Low:
  • Speculative: Local muscle injury and injection-site reaction; off-target blockade of related signaling proteins; nosebleeds and dilated skin vessels reported with broader pathway blockade; tendon and connective tissue lagging muscle gain; muscle quality falling as mass rises; immune response to a synthetic mirror-image peptide; worse outcomes if an undetected cancer is present; exposure to impure or misidentified material

Monitoring

Marker Target Why
Appendicular lean mass index (DEXA) Men ≥ 7.5 kg/m²; women ≥ 6.0 kg/m² The primary success measure — regional muscle mass
Creatine kinase (CK) 40–200 U/L Detects muscle fiber damage from injection trauma
High-sensitivity C-reactive protein (hs-CRP) < 0.5 mg/L Flags local or systemic inflammatory response to repeated injection
Serum myostatin (GDF-8) No established target; track change from the individual's own baseline The only direct read on whether the signal is actually being blocked
Estimated glomerular filtration rate (eGFR) > 90 mL/min/1.73 m² Peptide clearance depends on kidney function
Alanine aminotransferase (ALT) Men 10–30 U/L; women 8–25 U/L Baseline liver status before exposure to an unstudied compound
Complete blood count with platelets (CBC) Platelets 175–250 ×10⁹/L; hemoglobin 13.5–15.0 g/dL (men), 12.5–14.5 (women) Bleeding margin for intramuscular injection, and a check on the class bleeding signal
Glycated hemoglobin (HbA1c) 4.8–5.3% Myostatin-pathway blockade shifts glucose handling in human trials

Cadence: Baseline set before any exposure; safety subset repeated at 2 weeks and 4 weeks after first exposure, then every 3 months while use continues; body composition reassessed at 3 and 6 months; full panel annually thereafter.

Qualitative Assessment

  • Injection-site soreness, swelling, warmth or persistent lump, and how quickly each resolves
  • Girth of the treated limb measured at a fixed landmark, weekly
  • Performance in a fixed loaded movement — repetitions at a set weight, held constant
  • Tendon or joint discomfort during or after loading, the earliest sign that muscle is outpacing its attachment
  • Unexplained bruising, nosebleeds or new small red marks on the skin
  • Energy, sleep quality and recovery between training sessions