The Peptide Reference
The Peptide Reference
References
Illustrative label for Erythropoietin (EPO)
Reference/Glycoprotein hormone

Erythropoietin (EPO)

EPO · Red Blood Cell Stimulating Hormone

Indexed only
research use only

Glycoprotein hormone, essential, that drives red blood cell production. The kidneys make it in response to low oxygen; the recombinant human form carries FDA approval for anemia in chronic kidney disease and in chemotherapy patients. Binding at receptors on bone marrow cells promotes survival and maturation of red blood cell precursors, which raises oxygen-carrying capacity. Competitive sports ban it for its performance-enhancing effects.

Stimulates red blood cell productionIncreases oxygen-carrying capacityFDA-approved for anemia treatmentImproves endurance capacity
01

Overview

Glycoprotein hormone, essential, that drives red blood cell production. The kidneys make it in response to low oxygen; the recombinant human form carries FDA approval for anemia in chronic kidney disease and in chemotherapy patients. Binding at receptors on bone marrow cells promotes survival and maturation of red blood cell precursors, which raises oxygen-carrying capacity. Competitive sports ban it for its performance-enhancing effects.

Erythropoietin receptors (EPOR) on erythroid progenitor cells in bone marrow are the binding target, and occupancy switches on three interconnected signaling pathways: JAK2/STAT5, PI3K/AKT, and RAS/MAPK. Red blood cell precursors are then shielded from apoptosis and survive on that protection, erythroid proliferation and differentiation run faster, and hemoglobin production rises. Hypoxic stress can drive endogenous EPO production as much as 1000-fold higher, which is the oxygen-sensing regulatory system on display.

Evidence profileno typed references yet · R authored
Preclinical depthanimal and in-vitro literature0/3
Human evidencetrials and human observation0/3
Regulatory standingalways authored, never derived3/3
Three independent axes, never averaged. The status pill above reads only the human axis; the preclinical profile stands beside it.
02

Research indications

What the compound has been studied for, grouped by body system. Effect size is the reported magnitude where it was measured — not a recommendation.

Medical Indications (FDA-Approved)3
CKD-Related Anemia

Anemia arising from chronic kidney disease is the primary FDA-approved indication.

ungraded · Large
Chemotherapy-Induced Anemia

Carries FDA approval for anemia in cancer patients on chemotherapy.

ungraded · Large
Surgical Blood Loss

Applied in certain surgical settings to lower the need for blood transfusions.

ungraded · Moderate
Performance (Banned in Sports)2
Endurance Enhancement

Oxygen delivery to muscle rises and endurance capacity improves with it. WADA prohibits it.

ungraded · Large
Altitude Acclimatization

Adaptation to high altitude may come faster as red blood cell mass rises.

ungraded · Moderate
Illustrative label for Erythropoietin (EPO)
Quick factsreference only
Class
Glycoprotein hormone
Research status
Extensively studied
Chain length
165 residues
Molecular weight
30400 Da
Half-life
~25 h
Typical dose
50–300 IU/kg based on medical indication
Frequency
1–3 times weekly depending on response
Cycle length
Variable; ongoing medical therapy adjusted based on hemoglobin levels
Storage
2-8°C refrigerated; do not freeze; do not shake vials or syringes
03

Molecular data

Type
Glycoprotein hormone
Molecular weight
30400 Da
Chain length
165 residues
Half-life
1500 min
Targets
EPO receptor
Pathways
erythropoiesisinsulin signallingMAPK/ERKPI3K/Akt
Accumulation · t½ ≈ 25 h · 7 days
0.01.12.30d1d2d3d4d5d6d7
steady-state peak 2.06×90% reached 3.5 dOpen full plotter ↗

Levels in single-dose multiples. A shape, not a pharmacokinetic prediction.

04

Dosing reference

Doses reported in the literature and by suppliers. These are a record of what has been used in research — reference, never instruction.

ContextRouteAmountFrequency
CKD Anemia (medical)SubQ or IV50-100 IU/kg3x weekly
Chemotherapy Anemia (medical)SubQ150-300 IU/kg3x weekly
Maintenance (medical)SubQIndividualized1-3x weekly
05

Interactions

Iron supplementation

Hemoglobin production requires iron, which is often given alongside EPO therapy.

synergistic
TB-500

Mechanisms differ; no interactions known.

compatible
BPC-157

The mechanisms differ, and no interactions are known.

compatible
06

What to expect

Days 1-3Stimulation of bone marrow starts
Week 1-2Reticulocyte count rises
Week 2-4Hemoglobin starts to climb
Week 4-12With correct dosing, target hemoglobin is reached
07

Safety

raises blood pressurecarcinogenic risk

Mechanistic flags — properties of the pathway, not observed adverse events.

Commonly reported5
  • Injection site reactions
  • Headache
  • Hypertension
  • Joint pain
  • Flu-like symptoms
Stop and seek advice4
  • Pain in the chest, or shortness of breath
  • Blood clot signs — swelling in a leg, pain
  • Response to EPO abruptly lost
  • Severe headache, or a change in vision
Contraindications4
  • Uncontrolled hypertension
  • Prior pure red cell aplasia
  • Hemoglobin over 12 g/dL — cardiovascular risk rises
  • Malignancy that is active; a relative contraindication
08

Quality checklist

What to confirm before trusting a batch of research material. A verification aid — not an endorsement of any supplier.

Pre-sourcing self-audit0 / 7 confirmed
  • Third-party Certificate of AnalysisIndependent lab · dated · lot-matched.
  • HPLC purity ≥ 98%Reverse-phase trace included.
  • Mass-spec confirms 30400 g/molMALDI-TOF or ESI-MS.
  • Counterion stated (acetate ≫ TFA)TFA salts can confound bioassays.
  • Endotoxin / sterility statementRelevant once reconstituted.
  • Lyophilised · cold-chain shippedStored −20 °C, shipped on ice.
  • Labelled “research use only”No therapeutic or dosing claims.
Recorded signals for this compound · 9
Expected
  • ✓Clear, colorless solution
  • ✓Pharmaceutical grade product
  • ✓Seals and packaging intact
  • ✓Cold chain properly maintained
Caution
  • !Potency may be affected by temperature excursions
  • !Quality assurance is absent from research-grade products
Reject
  • ×Held at room temperature
  • ×Visible particulates
  • ×Solution cloudy or discolored
09

FAQ

Why does sport ban EPO when it holds FDA approval as a medicine?

FDA approval covers anemia in kidney disease and in chemotherapy patients, and nothing wider — the indications are narrow. The ban in sport follows from oxygen delivery being pushed far past medical therapeutic levels, which hands over an unfair endurance advantage. Doses taken by athletes produce performance effects vastly beyond anything used medically.

Which hemoglobin level makes EPO dangerous?

Guidelines hold hemoglobin under 11–12 g/dL during EPO therapy, since anything higher raises cardiovascular risk significantly — blood clots, stroke, heart attack. The ceiling is there because oxygen-carrying capacity turns harmful in excess, driving blood viscosity to dangerous levels.

Does the endurance gain from EPO come free of side effects?

Endurance capacity does improve, on greater red blood cell production and oxygen delivery. Water retention, joint pain, headaches, and hypertension are common alongside it. Of greater concern are thromboembolic events (blood clots) and a theoretical risk of tumor progression at the higher doses used for performance enhancement.

How long do the benefits last once EPO is stopped?

Effects start to fade as soon as injections stop, red blood cells having a natural 120-day lifespan. Within 2–3 weeks of discontinuation hemoglobin heads back toward baseline. Most of the performance benefit goes quickly, so sustained effect requires continued use, which is why athletes in endurance sport met testing challenges.

For research use only. Nothing on this page is medical advice, and no number here is a recommendation to dose.