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Specimen Atlas of Research Peptides85 plates · MIT
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78Plate 78Reviewed 2026-04-27

Testagen

Bioregulator Peptide

also known as Lys-Glu-Asp-Gly, KEDG

Short tetrapeptide (Lys-Glu-Asp-Gly) from the Khavinson bioregulator tradition, proposed as a testicular tissue-specific regulator. Animal models suggest support for testicular function and spermatogenesis; evidence remains limited to mechanistic and animal studies, with no human clinical trials or regulatory approval. In vitro, the peptide penetrates cell nuclei and shows sequence-specific interaction with deoxyribooligonucleotides and DNA. [fedoreyeva-2011]

Quick facts
Class
Bioregulator Peptide
Evidence level
Mechanistic animal evidence
Regulatory status
Not FDA-approved (US) — research use only
§ I

At a glance

Sequence
Lys-Glu-Asp-Gly
Localization
Nuclear
Tissue target
Testicular
Route

SQ · Abdomen · Cyclical

§ II

Mechanism

Edit ↗

Primary target — Testicular tissue; proposed nuclear DNA interaction.

Pathway — Nuclear penetration → DNA/oligonucleotide binding → gene expression modulation (bioregulator hypothesis) [fedoreyeva-2011].

Downstream effect — Proposed support for spermatogenesis and testicular function; mechanistic data limited to nuclear localization and DNA interaction [fedoreyeva-2011].

Origin — Khavinson bioregulator school — isolated from testicular tissue peptide fractions.

Feedback intact — Unknown — no HPG axis data.

§ III

Dosage

Protocols described in the cited literature; not medical advice.

Edit ↗
ParameterValue
Typical protocol (anecdotal)100–200 mcg / dayNo published human dosing studies; derived from Russian bioregulator practice.
FrequencyOnce daily or alternate days
Cycle length10–20 days on, 10–14 days offBioregulator tradition uses pulsed cycles; no controlled data.
Evidence basisAnimal mechanistic / in vitro only [fedoreyeva-2011]
RouteSubcutaneous
ReconstitutionSterile water or bacteriostatic saline
Half-lifeUnknown — likely minutes (short peptide)
§ III · b

Reconstitution

A pure mass-to-volume utility. Enter what you have in the vial; the atlas computes the volume per dose. No prescription information.

Inputs
mg
mL
mcg
The calculator does pure mass-to-volume math. It does not recommend a dose. Refer to Testagen's cited literature for protocol specifics.
Volumetric outputFig. C — reconstitution math
Volume per dose
0.100mL
10.0 units on a U-100 insulin syringe
Concentration
2500
mcg per mL
Doses per vial
20
at this dose

Evidence base: Russian-language clinical literature, primarily from the St. Petersburg Institute of Bioregulation and Gerontology (Khavinson school), 1985 onward. Not extensively peer-reviewed in Western journals.

§ V

Adverse events

Severities follow the FDA / CTCAE convention.

Edit ↗
Injection site reactionsmild
Erythema, mild irritation (potential)
Systemic effects
Unknown — no human safety data
Hormonal impact
No published data on testosterone, LH, FSH effects
Long-term safety
Unknown — no long-term studies
Absolute contraindications
  • Active testicular malignancy
Relative contraindications
  • Hormone-sensitive cancers (no data; theoretical caution)
  • Pregnant or breastfeeding (no data)
§ VI

Administration

Edit ↗
  1. 01
    Reconstitution

    Add 1–2 mL sterile or bacteriostatic water to lyophilised vial. Swirl gently; do not shake. Solution should be clear.

  2. 02
    Injection site

    Subcutaneous — abdomen or thigh. Rotate sites daily. Use standard insulin syringe (27–31G).

  3. 03
    Timing

    Morning or evening; no established optimal timing. Anecdotal preference: evening to align with circadian testosterone patterns.

  4. 04
    Storage

    Lyophilised: room temp, dark. Reconstituted: refrigerate 2–8 °C, use within 14–21 days if bacteriostatic water used.

  5. 05
    Cycle protocol

    10–20 days on, 10–14 days off. Bioregulator tradition uses pulsed exposure; rationale: prevent receptor/pathway desensitisation.

Reference Q&A

Frequently asked

Is Testagen FDA-approved?

Testagen is not FDA-approved in the United States and is handled as a research compound (research use only). Regulatory status may differ in other jurisdictions.

Appendix

Sources

27%

of 41 rendered claims carry a resolvable citation.

  1. [fedoreyeva-2011]
    Fedoreyeva 2011Penetration of short fluorescence-labeled peptides into the nucleus in HeLa cells and in vitro specific interaction of the peptides with deoxyribooligonucleotides and DNA.
    journal, 2011
Related plates
Plate composed 2026-04-27 · maturity human-reviewed · schema v1 · Contributors: peptidesdb-core · 30 fields uncited — open contributions