| Content | Clinical Test Expectation - Human Subjects : Increased growth hormone secretion and IGF-1 Levels with no increase in prolactin. Increased body weight and length through increased protein synthesis. Increased muscle growth and bone density. Improved immune function, cognition and memory. Increased collagen production, fat loss and cellular repair and regeneration.
Strength - 2MG per vial
Introduction
CJC-1295 is a synthetic GHRH (growth hormone releasing hormone) analogue made up of 30 amino acids. It has been found to be highly effective with regards to the increase of growth hormone secretion and IGF-1 without negatively affecting the pulsatility of GH secretion.
CJC-1295 is often combined with Ipamorelin due to its enhanced specificity as a GHRH. This peptide generates similar increases in growth hormone secretion, but without the appetite stimulation and increase in cortisol, acetylcholine, prolactin, and aldosterone seen with other peptides in its class. This peptide has been found to be very well-tolerated and perfect when combined with Ipamorelin.
CJC 1295 offers many benefits to the body, including:
- Increased growth hormone secretion and IGF-1 Levels with no increase in prolactin
- Increased Body Weight and Length through increased protein synthesis
- Increased Muscle Growth
- Increased Bone Density
- Improved Immune Function
- Improved Cognition and Memory
- Increased Collagen Production
- Increased Fat Loss
- Increased Cellular Repair and Regeneration
CJC-1295 also promotes slow wave deep sleep, which is responsible for the highest level of muscle growth and memory retention and rejuvenation.
Dosing Details
You inject 2ml water into the vial of CJC1295 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 (one unit) on the syringe each morning before breakfast, at lunch time and before bed, and inject it into the tummy under the skin into the fatty skin layer. It’s a total of 30 (3 units) on the syringe per day taken in three lots, before breakfast, lunch time and before bed.
How long will a vial last ?
A vial should last 7 days. | Clinical Test Expectation ACE-031 - Human Subjects : Massive increases in muscle mass and strength
Strength - 1MG per vial
Introduction
ACE-031 is a soluble form of activin receptor type IIB (ActRIIB). ACE-031 promotes muscle growth by binding to myostatin and other negative regulators of muscle mass.
The scientists are still figuring out what properties the peptide has , but we already know a number of beneficial effects of its use, including:
- acceleration of muscle gain process by blocking myostatin hormone;
- fat-burning effect. ACE-031 reduces the amount of leptin and thus increases the adiponectin level;
- improves the density of bones, thus making them more durable and less prone to fractures and other injuries;
- no side effects. The peptide is absolutely safe, when administered at dosages that do not exceed the norm, ACE-031 does not have any side effects. Very rarely there may be headaches and discomfort at the injection site.
Dosing Details
You inject 1.1ml water into the vial of ACE031 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 5 (half a unit) on the syringe each day in the morning and inject it into the muscle (Intra Muscular) at site of growth bilaterally (that is 2.5 into each side totaling 5) directly into muscle.
Alternative for easier use :You inject 2.1ml water into the vial of ACE031 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 day in the morning and inject it into the muscle (Intra Muscular) at site of growth bilaterally (that is 5 into each side totaling 10) Directly into muscle.
How long will a vial last ?
A vial should last 10 days. | Clinical Test Expectation Melanotan II - Human Subjects : Tanning the skin. Producing erections in men with ED (erectile dysfunction), when given as a shot under the skin
Strength - 10MG per vial
Introduction
Melanotan-II is a lab-made chemical that is similar to a hormone found in people. Be careful not to confuse melanotan-II with melatonin. Melanotan-II is given as a shot to produce erections in men with ED (erectile dysfunction), tan the skin, and prevent skin cancers caused by sun exposure.
This peptide is similar to a substance in our bodies, called “melanocyte-stimulating hormone,” which increases the production of skin-darkening pigments. Melanotan-II might also work in the brain to stimulate erections of the penis.
- Tanning of the skin, when given as a shot under the skin
- Producing erections in men with ED (erectile dysfunction), when given as a shot under the skin.
Melanotan-II is possibly safe when used under medical supervision for treating ED (erectile dysfunction). It may cause nausea, stomach cramps, decreased appetite, flushing, tiredness, yawning, darkened skin, spontaneous erections of the penis, and other side effects. This is why we suggest use in the evenings.
Dosing Details
you inject 2ml water into the vial of MT2 from the water vial. 1 full syringe is 1ml. you then wait for the vial powder content to dissolve and once dissolved and clear you draw out 10 (1 unit) on the syringe each night before bed and inject it into the tummy under the skin into the fatty skin layer - subcutaneously. The product would require you to spend at least 30 minutes in the direct sunlight for the first 3 days to activate the product. Thereafter you can use sunbed etc. for tanning.
How long will a vial last ?
A vial should last 15-20 days | 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 - Human Subjects : Reduces body fat. Stimulates lipolysis. Triggers fat release from obese fat cells
Strength - 2MG per vial
Introduction
AOD 9604 is a modified form of Growth Hormone, which is a 191 amino acid peptide. The last 15 amino acids (176-191) of the Growth Hormone polypeptide have been reproduced as a specific peptide and is called GH Frag 176-191 or AOD 9604.
This peptide is used for burning fat and medically assisted weight loss, and it has other benefits as well. Gland stimulated is the Pituitary Gland.
While it's best known as a fat-burning peptide, there are plenty of other benefits to using AOD-9604. Here are some to note:
- Reduces body fat
- Triggers fat release from obese fat cells predominantly more than lean ones
- Mimics the way natural growth hormone regulates fat metabolism
- No adverse effects on blood sugar or growth
- Stimulates lipolysis
- Inhibits lipogenesis (the transformation of non-fatty foods into body fat)
- Favorable cartilage repair and regenerative properties, especially when paired with peptide BPC 157
AOD-9604, also known as Tyr-hGH Frag 176-191, has been proven to have a strong fat-burning capacity without creating a desire to overeat. It doesn't affect blood sugar or tissue growth. (Heffernan 2001 Heffernan 2001, Ng 2000).
AOD-9604 activates degradation and fat burning (oxidation) by a method that doesn't use the hGH receptor; it has its own mechanism of action independent of hGH. Laboratory studies on rodents, pigs, dogs & humans have identified the AOD-9604 mechanism which triggers fat release from the obese fat cells predominantly and works to reduce the accumulation of new fat in fat cells as well as increase fat burning. What is extraordinary about the AOD-9604 is its ability to reduce abdominal fat stores.
The second most potent fat loss peptide is CJC-1295 since it leads to an increase in overall GH levels in the body (the opposite of what happens typically as individuals age).
This explains one of the reasons people have tended to gain fat as they get older. If your only goal is fat loss, it's usually best to avoid using products GHRP (GHRP-6, GHRP-2 or GHRH’s) because they may give you the side effects of increased hunger and raised cortisol. AOD-9604 does not increase hunger or raise cortisol.
Dosing Details
You inject 2ml water into the vial of AOD 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 30 (3 units) on the syringe each night before bed 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 days. | Clinical Test Expectation Gonadorelin - Human Subjects : In males - Delayed puberty. Infertility in males caused by pituitary or hypothalamus problems. In females - cause ovulation (release of an egg from the ovary) in women who do not have regular ovulation and menstrual periods
Strength - 5MG per vial
Introduction
Gonadorelin is another name for gonadotropin-releasing hormone (GnRH). It is a synthetic decapeptide prepared using solid phase peptide synthesis. GnRH is responsible for the release of follicle stimulating hormone and leutinizing hormone from the anterior pituitary.
Gonadorelin is responsible for the release of follicle stimulating hormone and leutinizing hormone from the anterior pitutitary. In the pituitary GnRH stimulates synthesis and release of FSH and LH, a process that is controlled by the frequency and amplitude of GnRH pulses, as well as the feedback of androgens and estrogens. The pulsatility of GnRH secretion has been seen in all vertebrates, and it is necessary to ensure a correct reproductive function. Thus a single hormone, GnRH, controls a complex process of follicular growth, ovulation, and corpus luteum maintenance in the female, and spermatogenesis in the male. Its short half life requires infusion pumps for its clinical use
The mechanism of action is systemic - Like naturally occurring gonadotropin-releasing hormone (GnRH), gonadorelin primarily stimulates the synthesis and release of luteinizing hormone (LH) from the anterior pituitary gland. Follicle-stimulating hormone (FSH) production and release is also increased by gonadorelin, but to a lesser degree. In prepubertal females and some gonadal function disorders, the FSH response may be greater than the LH response. For the treatment of amenorrhea, delayed puberty, and infertility the administration of gonadorelin is used to simulate the physiologic release of GnRH from the hypothalamus in treatment of delayed puberty, treatment of infertility caused by hypogonadotropic hypogonadism, and induction of ovulation in those women with hypothalamic amenorrhea. This results in increased levels of pituitary gonadotropins LH and FSH, which subsequently stimulate the gonads to produce reproductive steroids.
Dosing Details :
You inject 2ml water into the vial of Gonadorelin 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 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 7 days |
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