Tesamorelin – 2MG per vial

Clinical Test Expectation Tesamorelin - Human Subjects : Reduce Belly Fat. Also used to assist with HIV induced belly fat. Strength - 2MG per vial

Introduction Tesamorelin is a stabilized synthetic peptide analogue of the hypothalamic peptide, Growth Hormone Releasing Hormone (GHRH) indicated for the reduction of excess abdominal fat in HIV-infected patients with lipodystrophy. Lipodystrophy is a metabolic condition characterized by insulin resistance, fat redistribution, and hyperlipidemia associated with antiretroviral therapy for HIV infection.

Tesamorelin is made with growth hormone-releasing factor (GRF). Tesamorelin is used to reduce excess fat around the stomach that is caused by taking certain HIV medications. This condition is also called lipodystrophy (LYE-poe-DIS-troe-fee).

Dosing Details You inject 2ml water into the vial of Tesamorelin 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 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

How long will a vial last ? A vial should last 10 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 Epithalon - Human Subjects : Anti-aging by way of increased telomerase production, which also allows replication of DNA so the body can rejuvenate old cells and grow new cells. Strength - 10MG per vial

Introduction Epitalon's primary role is to increase the natural production of telomerase, a natural enzyme that helps cells reproduce telomeres, which are the protective parts of our DNA. This allows the replication of our DNA so the body can grow new cells and rejuvenate old ones.

Epitalon is a synthetic peptide, telomerase activator, and putative anti-aging drug, which was identified as the putative active component of a bovine pineal gland extract known as epithalamin. Most studies on epitalon and epithalamin have been conducted by the St. Petersburg Institute of Bioregulation and Gerontology, primarily overseen by Vladimir Khavinson, in Russia.

Epitalon (also spelled Epithalon or Epithalone) is a synthetic variation of Epithalamin; a peptide secreted in the pineal gland of the brain. The pineal gland is a small pea-shaped gland sometimes referred to as ‘the third eye.’ It is more famous for secreting melatonin, the hormone associated with regulating our sleep/wake cycles.

Epitalon, often touted as ‘the fountain of youth,’ is a peptide made of four amino acids. These are alanine, glutamic acid, glycine, and aspartic acid. Peptides are short-chain amino acids that comprise two to fifty chains, which differentiate them from proteins (proteins have more than fifty chains). This peptide increases the natural production of telomerase, an enzyme that aids cells in producing telomeres, the productive parts of our DNA. The production of telomeres helps the body to produce new cells and rejuvenate the old ones.

Unfortunately, as we age, our bodies produce less and less telomerase. This affects cell replication resulting in aging. Epitalon is designed to reverse this process. Vladimir Khavinson, who studied it and conducted human and animal trials for over 35 years. These trials proved that this peptide is quite effective in fighting aging.

Epitalon is part of the new age ‘peptide therapies,’ an emerging science that uses peptides to signal different cells in the body to trigger different chemical reactions. These reactions have far-reaching effects on wound healing, muscle building, weight loss, and anti-aging.

Dosing Details You inject 2ml water into the vial of Epithalon 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 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

Clinical Test Expectation IGF-1 LR3 - Human Subjects : Stimulates mass muscle growth. Benefits the heart (a muscle). Absorption of Chondroitin Sulfate and Glucosamine Sulfate (also found in Velvet Antler) that protects cartilage and joints. Regenerates nerve tissue. Helps burn fat. Increases protein transport into cells. Reduces protein breakdown. Improves the production of white blood cells. Strengthens the immune system. Decreases LDL cholesterol. Strength - 1MG per vial

Introduction Long LR3 IGF1 is mainly secreted by the liver as a result of stimulation by Human Growth Hormone (HGH). Almost every cell in the human body is affected by IGF1, especially cells in muscle, cartilage, bone, liver, kidney, nerves, skin, and lungs. In addition to the insulin-like effects, IGF1 can also regulate cell growth and development, especially in nerve cells, as well as cellular DNA synthesis. It is also considered to be the next big break through in theultimate fountain of youth.

IGF1-LR3 BENEFITS:

• Stimulates muscle growth and has been shown to benefit the heart (a muscle).
• Encourages the absorption of Chondroitin Sulfate and Glucosamine Sulfate (also found in Velvet Antler) that protects cartilage and joints.
• Regenerates nerve tissue.
• Helps burn fat, increases protein transport into cells, and reduce protein breakdown.
• Improves the production of white blood cells that strengthens the immune system.
• Decreases LDL cholesterol.

IGF1 LR3 is a hormone just like HGH, but IGF1 is the most important factor that the body produces. IGF1 is much more powerful than HGH.

IGF1 LR3 has been shown to increase the rate and extent of muscle repair after injury and increase the rate of muscle growth from training. Not only are existing muscle fibers repaired quicker, IGF1 LR3 is responsible for hyperplasia, an increase in the amount of muscle cells. Studies have shown that these gains are not lost after time.

Hyperplasia is the Holy Grail of performance enhancing benefits, and occurs when muscle fibers actually split, therefore creating more muscle fibers. Hypertrophy is simply an increase in the size of the existing muscle cell, and occurs from weight training. Hyperplasia plus hypertrophy equals a new breed of amazing athletes.

IGF-1 LR3 provides almost permanent muscle-creating, muscle-repairing, and anti-aging benefits and is totally undetectable. Do you think athletes are chomping at the bit to get their hands on this stuff?

The legitimate scientific world is following the proper protocols with regards to IGF-1, but the underground world is not bound by the same rules. Legitimate science – rightly so – is nowhere near ready to allow “us” to start using this stuff. But this isn’t the point.

The point is that there is a substance out there that scientists are cautiously touting as an instant muscle builder and a fountain of youth, and for some people this is all that they need to hear. These people aren’t going to wait – haven’t waited – for legit science to bless the use of IGF-1 LR3 for human consumption before they go out and inject themselves with it.

In 2004 the leading experts on the subject admitted that this gene therapy could already be in use, and that the technology and knowledge is such that the process to deliver it isn’t complicated. Two and a half years later this circle of knowledge, and use, is that much larger

Knowing how HGH was purloined by people who were too impatient to wait for legit science to do it’s thing, bodybuilders and real athletes did what they had to do to get it and use it, danger be damned. There’s no reason to think that the same situation isn’t occurring right now.

Dosing Details You inject 2ml water into the vial of IGF1-LR3 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 inject 10 (1 unit / 100mcg) on syringe into the muscle bilaterally. So this means directly into the muscle and bilaterally meaning you split the 10 (1 unit / 100mcg) on syringe into 5 (half a unit / 50mcg) on syringe 5 (half a unit / 50mcg) and 5 (half a unit / 50mcg) on syringe and inject into the corresponding body part on the alternative side of the body. Eg. Inject into the bicep on right arm 5 (half a unit / 50mcg) on syringe and then 5 (half a unit / 50mcg) on syringe into the left bicep  as an example.

How long will a vial last ? A vial should last 18 to 20 days.