GHRP-6 (Growth Hormone Releasing Peptide – 6) – 10mg per vial

Clinical Test Expectation GHRP-6 - Human Subjects : Fat loss. Muscle gain when used with anabolic steroid. Improved skin. Healing of injuries. Improved sleep. Reduction in Inflammation Strength - 10MG per vial

Introduction Research studies have shown that GHRP-6 stimulation of Growth Hormone secretion has a host of beneficial effects associated with increased growth hormone levels such as decreased body fat, increased muscle, and increased strength and stamina.

This product is a peptide that has a wide range of potential benefits. It is commonly used by bodybuilders and athletes to help increase muscle mass and strength. Additionally, GHRP-6 has been shown to help promote healing and recovery from injuries. One of the most exciting potential applications of GHRP-6 is its ability to help increase GH production. GH is a hormone that is essential for growth and development. However, GH levels decline as we age, which can lead to a decrease in muscle mass and strength, as well as an increased risk of age-related diseases.

This peptide has been shown to stimulate GH production in both young and old individuals. In one study, GHRP-6 was shown to increase GH levels by up to 400% in healthy young men (1). In another study, GHRP-6 was shown to increase GH levels by up to 34% in healthy elderly men (2).

In addition to its ability to increase GH production, GHRP-6 has also been shown to have several other potential benefits. For example, GHRP-6 has been shown to improve wound healing), increase bone density, and protect against liver damage.

GHRP-6 is a promising peptide with a wide range of potential benefits. However, more research is needed to fully understand its safety and efficacy.

GHRP-6 is a peptide that has a wide range of potential benefits. Researchers are still working to unlock all of its potential, but some of the potential benefits that have been identified so far include the following:

One of the most promising potential benefits of GHRP-6 is its ability to increase muscle mass. In one study, researchers found that rats who were treated with GHRP-6 saw an increase in muscle mass of up to 10%. While more research is needed to confirm these results in humans, they suggest that GHRP-6 could be a helpful tool for people looking to build muscle mass.

This peptide has also been shown to improve sleep quality. In one study, rats who were treated with GHRP-6 slept more soundly and for longer periods of time than those who were not treated with the peptide. While more research is needed to confirm these results in humans, they suggest that GHRP-6 could be a helpful tool for people looking to improve their sleep quality.

GHRP-6 has also been shown to reduce inflammation. In one study, rats who were treated with GHRP-6 had reduced levels of inflammation markers in their blood. While more research is needed to confirm these results in humans, they suggest that GHRP-6 could be a helpful tool for people looking to reduce inflammation.

The use of this peptide has been shown by researchers to improve healing. It helps in muscle repair during periods of deep sleep.

Side Effects GHRP-6 is a peptide that has been shown to increase levels of growth hormone in the body. However, it is also associated with a number of side effects, including:

• Increased appetite
• Nausea
• Headaches
• Dizziness
• Joint pain
• Fatigue
• Insomnia
• Increased blood pressure
• Increased heart rate
• Anxiety
• Depression

If you experience any of these side effects while taking GHRP-6, it is important to consult with your doctor.

Dosing Details You inject 3ml water into the vial of GHRP 6 from the water vial. 1 full syringe is 1ml. You then wait for the vial powder content to dissolve ON ITS OWN. DO NOT SHAKE THE VIAL TO MIX POWDER. Once dissolved and clear in colour you draw out 10 (1 unit) on the syringe each morning before breakfast, 10 (1 unit) before lunch and 10 (1 unit) before bed and inject it into the tummy under the skin into the fatty skin layer. This is a total of 30 (3 units) on the syringe a day.

How long will a vial last ? A vial should last 10 days

Clinical Test Expectation MOTS-c - Human Subjects : Promotes fatty acid metabolism in the liver, metabolic flexibility and homeostasis. Regulate mitochondrial energy. Protects against age and diet dependent insulin resistance and obesity and helps with weight loss. Promotes resistance to metabolic stress. Improves exercise capacity. Helps prevent  Osteoporosis. Improves glucose regulation and promotes cell differentiation to form osteoblasts Strength - 10MG per vial

Introduction MOTS-c is a mitochondrial-derived peptide described as a bioactive 16 amino acid peptide. This peptide is detected in circulation, so it is classified as a mitochondrial or metabolic hormone. It primarily targets fat and skeletal muscle.MOTS-c is a peptide encoded by the short open reading frame of the mitochondrial 12S rRNA gene. It is significantly expressed in response to stress or exercise and translocated to the nucleus, where it regulates the expression of stress adaptation-related genes with antioxidant response elements (ARE). MOTS-c mainly acts through the Folate-AICAR-AMPK pathway, thereby influencing energy metabolism, insulin resistance, inflammatory response, exercise, aging and aging-related pathologies. Because of the potential role of MOTS-c in maintaining energy and stress homeostasis to promote healthy aging, especially in view of the increasing aging of the global population, it is highly pertinent to summarize the relevant studies. This review summarizes the retrograde signaling of MOTS-c toward the nucleus, the regulation of energy metabolism, stress homeostasis, and aging-related pathological processes, as well as the underlying molecular mechanisms.

Research done on this peptide has shown beneficial effects in reducing diabetes and obesity while also enhancing performance and longevity. Why does this happen? MOTS-c assists proper mitochondrial function, and the mitochondria are the energy center of every cell in the human body. Research has shown that MOTS-c is an exercise-mimetic peptide, meaning it makes the body think it is exercising even when it is not.

Benefits of MOTS-c

• Regulates mitochondrial energy
• Promotes the metabolism of fatty acid in the liver
• Promotes metabolic homeostasis
• Improves glucose regulation
• Aids in the resistance of metabolic stress
• Protects against insulin resistance
• Promotes weight loss
• Improves physical performance

Dosing Details You inject 1ml water into the vial of MOTS-c from the water vial. 1 full syringe is 1ml. You then wait for the vial powder content to dissolve ON ITS OWN. DO NOT SHAKE THE VIAL TO MIX POWDER. Once dissolved and clear in colour you draw out 50 (5 units) on the syringe and inject into stomach sub cutaneous 2 times a week evenly spaced in days.

How long will a vial last ? A vial should last 7 days.

Clinical Test Expectation - Human Subjects : Super fast joint, tendon, ligament healing. Heal wounds in internal organs, muscles, ligaments, tendons, skin, internal lacerations from surgery Strength - 5MG per vial

Introduction BPC 157, a pentadecapeptide derived from human gastric juice, has been demonstrated to promote the healing of different tissues, including skin, muscle, bone, ligament and tendon in many animal studies. Stable gastric pentadecapeptide BPC-157 is is a synthetic peptide chain. A peptide is simply a sequence of amino acids. BCP specifically is composed of 15 amino acids derived from a protective protein found in the stomach. BPC, short for 'body protective compound', is already found in human gastric juices in small amounts to heal the gut, but can be taken supplementally to benefit anywhere in the body. BPC-157 is a cytoprotective compound, meaning its actions include aiding the healing process including remodeling and protective effects. It can also protect against oxidative stress.

Dosing Details You inject 2ml water into the vial of BPC 157 from the water vial. 1 full syringe is 1ml. You then wait for the vial powder content to dissolve ON ITS OWN. DO NOT SHAKE THE VIAL TO MIX POWDER. Once dissolved and clear in colour you draw out 25 – 30 (two and a half to 3 units) on the syringe each morning before breakfast and inject it into the tummy under the skin into the fatty skin layer.

How long will a vial last ? A vial should last 7-8 days.

Clinical Test Expectation - Tirzepatide - Human Subjects : Aids type 2 diabetis. Assist with large scale weight loss. Strength - 2MG per vial

Introduction Historically, the treatment of obesity focused almost exclusively on lifestyle-based approaches. However, evidence that diet and exercise prompt physiological counterregulatory mechanisms that limit weight reduction and impede weight maintenance has led to the realization that obesity is a complex, multicomponent metabolic disease of energy homeostasis involving central and peripheral mechanisms. Once obesity is present, those mechanisms render a return to lower weight difficult. Accordingly, several clinical guidelines now recommend treatment with antiobesity medications for people with obesity or for those with overweight and weight-related complications. Recent studies with long-acting glucagon-like peptide-1 (GLP-1) receptor agonists demonstrated that greater efficacy with acceptable safety could be achieved by targeting the pathways of endogenous nutrient-stimulated hormones. Glucose-dependent insulinotropic polypeptide (GIP), another nutrient-stimulated hormone, regulates energy balance through cell-surface receptor signaling in the brain and adipose tissue. A molecule that combines both GIP and GLP receptor agonism theoretically may lead to greater efficacy in weight reduction.

Tirzepatide is a once-weekly subcutaneous injectable peptide (approved by the Food and Drug Administration [FDA] for type 2 diabetes) engineered from the native GIP sequence, with agonist activity at both the GIP and GLP-1 receptors. Preclinical data demonstrated that the affinity of tirzepatide for GIP receptors was equal to the affinity of native GIP for GIP receptors, whereas tirzepatide bound GLP-1 receptors with affinity approximately five times weaker than native GLP-1 bound GLP-1 receptors. GIP activation appeared to act synergistically with GLP-1 receptor activation to allow greater weight reduction in humans than that achieved with GLP-1 receptor monoagonism. In phase 2 studies in people with type 2 diabetes, tirzepatide induced clinically relevant weight reduction, warranting further investigation for the treatment of obesity. The present trial, SURMOUNT-1, evaluated the efficacy and safety of tirzepatide in adults with obesity or overweight who did not have diabetes with great success

Dosing Details You inject 1ml water into the vial of Tirzepatide from the water vial. 1 full syringe is 1ml. You then wait for the vial powder content to dissolve ON ITS OWN. DO NOT SHAKE THE VIAL TO MIX POWDER. Once dissolved and clear in colour you draw out the entire vial and inject it into the tummy under the skin into the fatty skin layer. A vial should last 1 usage once a week.

How long will a vial last ? A vial should last 7 days.

Clinical Test Expectation Ipamorelon - Human Subjects : Reduction in body fat around the midsection. Improved muscle strength and mass. Strengthened bones. Repaired joints and ligaments. Improved skin quality. Increased energy and vitality Strength - 2MG per vial

Introduction Ipamorelon assists with reduction of weight around the midsection and moderate lean clean muscle gains.

Once Ipamorelins injections are administered, a selective pulse is sent to the brain that stimulates the hypothalamus and anterior pituitary to release growth hormones. Once this pulse is sent, the cells go directly to the muscle to support development while staying clear of any possible bone or cartilage growth. When Ipamorelins peptides release growth hormones, the cells go straight to the muscle to support its larger development and seem to steer clear of any possible bone or cartilage distortions.

Ipamorelon injections will increase cell synthesis, elevate secretion levels of insulin from pancreatic tissue, and increase ghrelin in the stomach—which helps release GH and control hunger. All of these functions work to promote fat loss, shuttling of nutrients, and building clean muscle mass.

Ipamorelin has been gaining popularity amongst body builders as the most effective growth-hormone releasing peptide available. While more clinical research is still needed, some of the benefits of Ipamorelin include:

• Reduction in body fat
• Improved muscle strength and mass
• Strengthened bones
• Repaired joints and ligaments
• Improved skin quality
• Increased energy and vitality

It should be emphasized that Ipamorelin is not only the most efficient, but also the safest and selective GH stimulant. That’s because Ipamorelin stimulates growth hormones without having an effect on the blood levels of prolactin and cortisol. This feature makes Ipamorelin attractive for bodybuilders, and why it is arguably the best option from among all peptides stimulating the GH production.

Dosing Details You inject 2ml water into the vial of Ipamorelin from the water vial. 1 full syringe is 1ml. You then wait for the vial powder content to dissolve ON ITS OWN. DO NOT SHAKE THE VIAL TO MIX POWDER. Once dissolved and clear in colour you draw out 10 (1 unit) on the syringe each morning before breakfast, 10 (1 unit) each day before lunch, and 10 (1 unit) each day before bed. So a total of 30 (3 units) on the syringe a day, you inject it into the tummy under the skin into the fatty skin layer.  The doses respectively can be increased after a week from 10 (1 unit) to 15 (one and a half units) on syringe respectively ie. 45 (four and a half units / 450mcg) on syringe a day in total.

How long will a vial last ? A vial should last 5 days.

Clinical Test Expectation GHK-cu - Human Subjects : Wound healing and antiaging skin care ++. Antioxidant and Anti-Inflammatory Properties. Stimulates Blood Vessel Growth. Increases Neurotrophins. Gene Regulator. Reverse Gene Silencing Strength - 100MG per vial

Introduction The human peptide GHK-cu (glycyl-l-histidyl-l-lysine) has multiple biological actions, all of which, according to our current knowledge, appear to be health positive. It stimulates blood vessel and nerve outgrowth, increases collagen, elastin, and glycosaminoglycan synthesis, as well as supports the function of dermal fibroblasts. GHK’s ability to improve tissue repair has been demonstrated for skin, lung connective tissue, boney tissue, liver, and stomach lining. GHK has also been found to possess powerful cell protective actions, such as multiple anti-cancer activities and anti-inflammatory actions, lung protection and restoration of chronic obstructive pulmonary disease (COPD) fibroblasts, suppression of molecules thought to accelerate the diseases of aging such as NFκB, anti-anxiety, anti-pain and anti-aggression activities, DNA repair, and activation of cell cleansing via the proteasome system. Recent genetic data may explain such diverse protective and healing actions of one molecule, revealing multiple biochemical pathways regulated by GHK.

Dosing Details You inject 2ml water into the vial of GHK cu from the water vial. 1 full syringe is 1ml. You then wait for the vial powder content to dissolve ON ITS OWN. DO NOT SHAKE THE VIAL TO MIX POWDER. Once dissolved and clear blue in colour you draw out 20 (2 units) on the syringe each morning before breakfast and inject it into the tummy under the skin into the fatty skin layer.

How long will a vial last ? A vial should last 10 days.