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GH Peptide

Follistatin-315

315-amino-acid isoform of follistatin glycoprotein (~38 kDa). Extended circulating half-life (~10 days) due to lower heparan sulfate proteoglycan binding compared to FS-288 isoform. Subcutaneous administration.

Emerging Evidence
~10 days
Half-Life
70%
Bioavailability
100–300 mcg/day
Typical Dose
SubQ
Routes

Overview

Follistatin-315 is a growth hormone-related peptide. 315-amino-acid isoform of follistatin glycoprotein (~38 kDa).

With a half-life of ~10 days (240 hours), Follistatin-315 supports less frequent dosing schedules. Administered via SubQ injection, it has a bioavailability of approximately 70% via its primary route.

Extended circulating half-life (~10 days) due to lower heparan sulfate proteoglycan binding compared to FS-288 isoform. Subcutaneous administration. One-compartment model.

Mechanism of Action

Follistatin-315's pharmacological activity involves the following key pathways:

GH Axis Modulation

Follistatin-315 interacts with the growth hormone axis to influence GH-related signaling pathways.

Pharmacokinetics

Parameter Value
Half-Life ~10 days (240 hours)
Bioavailability ~70%
Time to Peak ~12 hours
Duration of Activity ~21 days
Routes Subcutaneous

Dosing Protocols

The following protocols represent commonly observed dosing patterns. These are observational summaries, not recommendations.

Standard Protocol
Dose 100 mcg/day
Route Subcutaneous
Frequency Once weekly
Duration 4-12 weeks
Higher-Dose Protocol
Dose 300 mcg/day
Route Subcutaneous
Frequency Once weekly
Duration 4-12 weeks

Reconstitution Steps

Follistatin-315 is supplied as a lyophilized (freeze-dried) powder and requires reconstitution before use. Common vial sizes: 1 mg, 5 mg.

  1. 1
    Gather Supplies

    Collect the Follistatin-315 vial, bacteriostatic water, alcohol swabs, a mixing syringe, and insulin syringes for dosing. Ensure all items are stored properly and unexpired.

  2. 2
    Swab Vial Tops

    Wipe the rubber stopper of both the Follistatin-315 vial and bacteriostatic water vial with alcohol swabs. Allow to air dry for 10 seconds before proceeding.

  3. 3
    Add Bacteriostatic Water

    Draw 1 mL of bacteriostatic water and inject it slowly down the inside wall of the Follistatin-315 vial. Follistatin is a delicate protein — never spray directly onto the lyophilized powder.

  4. 4
    Dissolve Gently

    Allow the water to dissolve the powder naturally over 2–3 minutes. Gently roll the vial between your palms if needed. Do not shake or agitate, as follistatin can denature easily.

  5. 5
    Verify Solution Clarity

    The reconstituted solution should be clear and colorless. If particles or cloudiness persist after gentle swirling, the peptide may have degraded and the vial should not be used.

  6. 6
    Store and Draw Doses

    Store the reconstituted vial upright in the refrigerator at 2–8°C. For a 1 mg vial reconstituted with 1 mL, each 10 units on a 100-unit insulin syringe equals 100 mcg.

Quick Reconstitution Math

1 mg vial + 1 mL bac water = 1,000 mcg/mL. For a 100 mcg dose, draw 10 units on a 100-unit insulin syringe. Use the Milligram reconstitution calculator for custom vial sizes.

Reconstituted Follistatin-315 is stable for up to 14 days refrigerated at 2–8°C. Follistatin is a larger protein and more fragile than smaller peptides — avoid repeated freeze-thaw cycles and excessive agitation.

Frequently Asked Questions

What is Follistatin-315 and how does it work?
Follistatin-315 is the circulating isoform of the follistatin glycoprotein, functioning as a potent antagonist of myostatin and activin. It binds to these proteins with high affinity, forming complexes that prevent them from reaching their cell surface receptors, effectively removing the brake on skeletal muscle growth. FS-315 is the serum-based isoform generated when the precursor FS-344 undergoes proteolytic cleavage after injection.
What is the half-life of Follistatin-315?
Follistatin-315 has a circulating half-life of approximately 3 hours, which is longer than the FS-288 isoform due to its reduced heparin-binding affinity. This relatively short half-life means daily subcutaneous injections are commonly used to maintain effective circulating levels. Pharmacokinetic steady state is reached within approximately 1 day of consistent dosing.
How long does Follistatin-315 take to show results?
Grip strength improvements have been observed as early as 7 days in research settings. Measurable changes in lean mass and body composition are typically reported over 4–8 weeks of consistent administration. The most commonly reported protocol duration is 10–30 days per cycle, with results continuing to develop in the weeks following completion.
What is the difference between Follistatin-315 and Follistatin-344?
FS-344 is the precursor form commonly used in gene therapy, while FS-315 is the active circulating isoform generated after FS-344 undergoes post-translational cleavage. FS-315 has a 10-fold lower affinity for cell surface heparin sulfate proteoglycans compared to FS-288, which means it circulates more freely in serum and preferentially targets skeletal muscle tissue rather than the pituitary–gonadal axis.
Does Follistatin-315 affect reproductive hormones?
The FS-315 isoform is considered to have a more favorable profile regarding reproductive function compared to FS-288. Because FS-315 has reduced affinity for heparin and cell surfaces, the gonadal–pituitary axis is much less likely to be affected. This tissue selectivity is one of the primary reasons FS-315 is the preferred isoform in research and clinical applications.
How is Follistatin-315 typically dosed and cycled?
The most commonly observed protocol involves 50–100 mcg per day administered subcutaneously for 10–30 consecutive days, followed by 3–4 weeks off. Cycling is considered important due to the potent nature of myostatin inhibition. Human injectable data remains limited, with most published evidence coming from animal models and gene therapy clinical trials.

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