| Content | 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. | Clinical Test Expectation - Human Subjects CJC-1295 DAC : Long Release - 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 DAC is often used to stimulate muscle development. This works by increasing the blood level of hormones associated with growth. It can increase muscle mass and strength, decrease body fat, improve injury recovery time, and even improve sleep quality and cognitive function.
CJC-1295 + DAC has shown some amazing results as a growth hormone releasing hormone (GHRH) analog. Not only has CJC-1295 shown the ability to increase growth hormone and IGF-I secretion and its benefits, but it has been able to do so in very large amounts. Recent research studies have shown that CJC - 1295 stimulates GH and IGF-1 Secretion, and will keep a steady increase of HGH and IGF-1 with no increase in prolactin, leading to intense fat loss, and increases protein synthesis.
CJC-1295 + DAC is a long acting Growth Hormone Releasing Hormone, which causes the anterior pituitary to release more growth hormone. GHRH is released in pulses in the body, which alternate with corresponding pulses of somatostatin (growth-hormone inhibiting-hormone). Clinical Research was first conducted for CJC-1295 during the mid-2000s. The objective of the peptide was to treat visceral fat deposits in obese AIDS patients, as increased levels of exogenous HGH are presumed to increase lipolysis (fat loss). The clinical research was ultimately successful for most research subjects. Ghrelin, released from the gut, which circulates and acts as a hunger hormone, has synergistic activity in the body with GHRH and also suppresses somatostatin to make way for the GHRH pulse. Studies shows that combining a GHRP-6 with CJC-1295 + DAC, significantly increase the release of GH and IGF-1 production without an increase in prolactin. An example of a GHRP (GH Releasing Peptide) is Hexarelin or GHRP-2. CJC-1295 + DAC is a exceptionally designed peptide and is known for being the finest of the hGH secretogues. The DAC (Drug Affinity Complex) portion increases the half-life by binding with serum albumin and protects the CJC-1295 DAC peptide from degradation. This was formed when a lysine link was bounded to DACs to a reactive chemical called maleimidoproprionic acid (MPA).
Dosing Details
You inject 2.5ml water into the vial of CJC1295 DAC 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 60 (6 units) on the syringe twice a week evenly spaced on the days each morning before breakfast and inject it into the tummy under the skin into the fatty skin layer. A vial should last 2 weeks.
How long will a vial last ?
A vial should last 14 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 | Clinical Test Expectation - Human Subjects : Reducing fibrosis in acute and chronic diseases like heart failure, lung inflammation, and the kidneys. Aids Sperm motility, testicular descent, joint health, preeclampsia, wound healing
Strength - 6MG per vial
Introduction
B7-33 exibits potent anti-fibrotic effects. It is under active research and investigation as a means of reducing fibrosis in acute and chronic diseases like heart failure, lung inflammation, kidney and more. In animal studies, B7-33 has reduced fibrosis by roughly 50%, leading to prolonged survival following injury and offering the first new means of treating heart failure in 20 years. It has been shown to reduce excessive scar formation following cardiac injury. It has also shown promise in the treatment of certain vascular disorders as well as preeclampsia of pregnancy.
Due to its unique structure, even though B7-33 binds to the RXFP1 receptor with greater affinity than the native H2-relaxin protein, B7-33 preferentially activates the pERK pathway over the cAMP pathway. The pERK pathway is known to play an important role in cell cycle arrest in the G1 phase and has been implicated in a number of diseases including protein-misfolding conditions like Alzheimer’s disease and Crutzfeld-Jacob disease. By arresting cell cycle progression in cells with RXFP1 receptors, B7-33 can produce a number of effects. It appears that its anti-fibrotic effects, however, are most likely mediated through the ability to stimulate RXFP1-angiotensin II type 2 receptor heterodimering, which activates pERK1/2 signaling and, eventually, leads to increased production of the collagen-degrading enzyme matrix metalloproteinase (MMP) -2. It is important that B7-33 promotes only pERK pathway activation as it is thought that cAMP activation may be responsible for some of the tumor-promoting effects seen with full-sequence H2-relaxin and not seen with B7-33
Dosing Details
You inject 2ml water into the vial of B7-33 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 0.25 – 0.3 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 GHRP-2 - Human Subjects : Stimulation of GH secretion. Appetite promotion. Fat mass decrease. Lowering of cholesterol level. Skin and bones state improvement. Defence of the liver and anti-inflammatory action. Aid flexibility and joint health. Promotes better recovery from injuries and training. Improve sleep. Enhanced Anti-aging benefits. Accelerates growth of muscle tissue and reduces body fat. Promotes significant increase in strength and endurance.
Strength - 10MG per vial
Introduction
Growth Hormone Releasing Peptide-2 (GHRP-2), also known as Pralmorelin, is a synthetically made growth hormone secretagogue, a peptide that stimulates the body to increase natural production of growth hormone. GHRP-2 is an agonist of ghrelin, a gut peptide and also known as “the hunger hormone”, which binds to the growth hormone secretagogue receptor. Ghrelin has been shown to stimulate growth hormone secretion and appetite initiation.
GHRP-2 is used to increase muscle mass, decrease body fat, and enhance flexibility and joint health. GHRP-2 also promotes better recovery from injuries and training. GHRP-2 is also functions to improve sleep, enhance anti-aging benefits, and improved overall health and wellness. Higher growth hormone levels also lead to greater production of IGF-1 in the body, which improves in lean body composition, accelerates growth of muscle tissue and reduces body fat. GHRP-2 promotes significant increase in strength and endurance, especially when used long term. Athletic performance, physical capacity, and aging-related decline all have the ability to improve drastically with the use of this peptide.
GHRP-2 is widely regarded as one of the most effective growth hormone releasing peptides for both athletic performance and anti-aging effects. It promotes substantial increases in the body’s output of growth hormone while minimizing the powerful hunger side effects associated with GHRP-6. This may lead to significant improvements in lean body composition.
GHRP-2 works to enhance natural growth hormone production in two ways. First, the GHRP-2 intensifies the natural growth hormone releasing signal, resulting in a substantial secretion of growth hormone. Second, it suppresses a hormone in the body called somatostatin, also known as growth hormone inhibiting hormone (GHIH). Somatostatin generates the body to decrease its natural growth hormone production. By restricting the activity of somatostatin, GHRP-2 can improve growth hormone creation, resulting in increased natural growth hormone levels. GHRP-2 also activates ghrelin, a peptide hormone produced in the gastrointestinal system, which has strong effects on growth hormone production and appetite.
As GHRP-2 stimulates the body to create growth hormone, there is no shutdown of natural growth hormone production as occurs with synthetic hGH administration. GHRP-2 causes growth hormone secretion in a manner that firmly resembles natural release patterns, instead of being continually raised. This method prevents many of the negative side effects of synthetic hGH administration, including the shutdown of natural growth hormone production.
Dosing Details
You inject 3ml water into the vial of GHRP 2 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 |
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