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Superior Peptide Ipamorelin

IPAMORELIN (Growth Hormone Releasing Penta Peptide) 5 mg x 1 vial – Superior Peptide

2,600.00
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TESAMORELIN + CJC-1295 + IPAMORELIN (Ripping Blend) 12 mg x 1 vial – Superior Peptide

3,700.00
Superior Peptide Ripping Blend

Description

Superior Peptide MOD GRF (1-29), also known as Modified Growth Hormone-Releasing Factor (1-29), is a synthetic analog of the natural growth hormone-releasing hormone (GHRH). It is designed to stimulate the pituitary gland to produce and release human growth hormone (HGH) in a more efficient manner than the natural hormone.

Mechanism of Action:

MOD GRF (1-29) works by binding to the GHRH receptors in the pituitary gland, leading to an increase in the secretion of HGH. This can potentially enhance growth, fat loss, and muscle gain, which is why it attracts interest within the bodybuilding community.

Benefits in Bodybuilding:

  1. Increased Muscle Mass: By stimulating HGH release, MOD GRF (1-29) may help increase lean muscle tissue.
  2. Fat Loss: Enhanced HGH levels can contribute to fat metabolism, promoting lean body composition.
  3. Recovery: Increased levels of GH can aid in recovery from workouts and may reduce muscle soreness.
  4. Improved Sleep: Some users report better sleep quality, which is crucial for recovery and performance.

Results:

The results can vary significantly among individuals based on several factors, including dosage, frequency of use, diet, exercise regimen, and overall lifestyle. Some users may report noticeable gains in muscle mass and decreased body fat within a few weeks, while others may see more gradual changes over a longer duration.

Doses:

  • Common dosages: MOD GRF (1-29) is typically used at doses ranging from 100 to 300 micrograms, administered subcutaneously or via injection.
  • Timing: Many users take it 20-30 minutes before workouts or just before bedtime to utilize its efficacy in boosting HGH release.

Cycle:

  • Bodybuilders often use MOD GRF (1-29) in cycles of 8 to 12 weeks, followed by a break to prevent desensitization of the GH receptors.

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