PE-22-28 – 10mg per vial

Clinical Test Expectation PE-22-28 - Human Subjects : Anti depressant. Stroke Recovery.TREK-1 inhibitor. Assists with mood, memory and learning. Aids muscle function Strength - 8MG per vial

Introduction This peptide has been found to be a natural and fast-acting therapeutic peptide that may treat depression better than other TREK-1 blockers. The optimal PE-22-28 dosage for depression is shown below. While its effectiveness has been proven, PE-22-28 is a new peptide that does not have a published study involving human subjects. Presently, experiential data suggests that PE-22-28 may possess almost no harmful side effects while being equally or more effective than current and classic antidepressants.

This peptide are natural peptides, which generally have higher levels of safety than most antidepressants. Additionally, unlike prescription antidepressants, natural peptides do not provoke withdrawal behavior when no longer used. Moreover, PE-22-28 is fast-acting. Currently, marketed antidepressant drugs often take several weeks to become effective. PE-22-28 only needs four days to exert their effects. Additionally, PE-22-28 is effective regardless of how it is administered.

While research and data collection continues, this peptides benefits look promising. And with the growing public awareness of the importance of mental health, PE-22-28 offers a potential new way to envision depression treatment without the harmful health risks.

Dosing Details You inject 2ml water into the vial of PE 22-28 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 (2.5 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 - 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.

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 HMG - Human Subjects : In women - Assist with conceiving, and fertility. In Men - Increase production of natural testosterone. Assist with testicular dystrophy. Increased libido. Post Cycle Therapy (PCT) for men and women Strength - 75iu per vial

Introduction HMG peptide vial is Human Menopausal Gonadotropin synthetic peptide. It is a hormonal medicine that helps treat fertility disorders in both men and women. A woman can be injected with this peptide and it will stimulate follicle-stimulating hormone (FSH) and luteinizing hormone (LH) that are responsible for maturation of female eggs and thus ovulation.

In men, it stimulates testosterone production which is responsible for the formation and maturation of sperm.HMG is a synthetic peptide for men or women with fertility problems, research has suggested it would enable them conceive.

Research has suggested this peptide stimulates the sex hormone follicle-stimulating hormone and luteinizing hormone. A woman who is undergoing reproduction fertility treatment this peptide begins to ovulate. It stimulates the production of the hormones and also increases FSH and LH in the body.

Laboratory research in mice suggests hmg human menopausal gonadotropin brings back fertility almost immediately the injection does vary from one person to the other. It brings some mild effects that will resolve after some time.

Research shows that when men are injected with HMG it works like human chorionic Gonadotropin. The peptide will stimulate the pituitary gland so that testosterone production is increased in the body. Research has suggested this is essential especially for a man that has undergone anabolic steroid therapy, as it aids the body to recover quickly.

Originally, the peptide known as HMG (Human Menopausal Gonadotropin) was developed to assist women in conceiving. It is a fertility medication that stimulates the production of lh and fsh hormones in a woman’s body, increasing her chances of ovulation. However, the compound’s use has evolved, and it is now used by men as well.

It has the ability to boost natural testosterone production in male patients. In addition, those who suffer from male health problems, such as testicular dystrophy, frequently report that their libidos are more potent and virile while on HMG treatment. After all, testosterone deficiency frequently contributes significantly to sexual dysfunction and impairs men in other ways, robbing them of vital energy, muscle mass, and youthful appearance, which is why a testosterone booster such as HMG has the potential to improve men’s lives significantly!

Female health: FSH and LH hormones are the components of this medication. It improves the likelihood of egg development in women who are having difficulty ovulating naturally (or in females who are ovulating sporadically). HMG is sold under various brand names, including Letrozale, Repronex, and Menopur, among others to help improve pregnancy chances. This medication may be used in conjunction with in vitro fertilization and intrauterine insemination.

Male health: The majority of men consider HMG therapy as an alternative to HCG therapy (Human Chorionic Gonadotropin). It is frequently used to boost the body’s natural testosterone levels. FSH and LH, the hormones contained in HMG, act on the testes through the pituitary gland. FSH is beneficial because it stimulates spermatogenic tissue in the testicles. In males, LH helps to stimulate intra-testicular synthesis.

Post Cycle Therapy: Typically, bodybuilders use this injectable medication to gain access to its combination of two female hormones. It is used in Post Cycle Therapy (PCT) to aid the body’s recovery following anabolic steroid therapy. It works by re-establishing normal bodily functions and improving sexual health following steroid use. Males who use anabolic steroids frequently experience testicular problems. For example, some men suffer testicular atrophy after using performance enhancers to gain muscle mass for an extended period, such as years. Males who wish to avoid these complications may begin HMG therapy following the cessation of anabolic steroid therapy. Men generally choose HMG because it includes hormones that stimulate the testes to produce testosterone without the drawbacks associated with HCG. HCG acts as a synthetic LH, whereas HMG is an amalgamation of actual hormones that will not cause an inability to respond to LH (which may happen with HCG).

Dosing Details You inject 2ml water into the vial of HMG 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 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 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.

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 Adipotide - Human Subjects : Faster muscle mass growth, superior fat-burning power Strength - 5MG per vial

Introduction Adipotide is a synthetic peptide that possesses anti-obesity properties. this peptide particularly targets and destroys specific proteins that constitute the surface of blood vessels that support white fat (adipose) tissue hence interfering with the supply of blood to the fat cells and resulting in their adoptosis (reabsorption and metabolization). Adipotide was initially referred to as Prohibitin-TP01 (Prohibitin-Targeting Peptide 1). It is a peptidomimetic that was synthesized by American scientists as a potential therapeutic drug for obesity and its amino acid sequence is CKGGRAKDC-GG-D(KLAKLAK)2. Adipotide has a molecular formula of C111H204N36O28S2. Peptidomimetics are tiny protein like chains that imitate peptides. It is an experimental drug for weight loss. It was developed in a way that enables it to bind to two receptors, prohibitin and ANXA2 which are found in blood vessels that support white adipose tissue. In rat and monkey based experiments, Adipotide has been shown to bring about rapid weight loss in both mice and rhesus monkeys. In general, Adipotide has been observed to bring about weight loss by reducing fat tissue especially in the abdominal region), rapid metabolic changes, and decreased food intake.

Dosing Details ADIPOTIDE – Week 1 : You inject 2ml water into the vial of Adipotide 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 15 (one and a half units) on the syringe each morning before breakfast and inject it into the tummy under the skin into the fatty skin layer. A vial should last 14 days. ADIPOTIDE – Week 2 to 4 :You inject 2ml water into the vial of Adipotide 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 morning before breakfast and inject it into the tummy under the skin into the fatty skin layer. A vial should last 7 days. Alternative Salon usage : You inject 4ml water into the vial of Adipotide 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 and inject 15 (one quarter of drawn amount) into each corner of the areas you want to be affected, for client. A vial should last 7 days.

How long will a vial last ? A vial should last 7 to 14 days