Raw Peptide Powder Triptorelin Acetate

Product Name: Triptorelin Acetate
Alias: GnRH,Decapeptyl,Triptorelin
CAS: 57773-63-4
MF: C64H82N18O13
MW: 1311.45
Purity: 99%
Grade: Pharmaceutical Grade
Appearance: White Powder
Specification: 2mg/vial

Storage: Lyophilized peptides although stable at room temperature for 3 months, should be stored desiccated below -18 dec. Upon reconstitution of the peptide it should be stored at 4 dec. between 2-21 days and for future use below -18 dec.

Triptorelin, a decapeptide,is a gonadotropin-releasing hormone agonist (GnRH agonist) used as the acetate or pamoate salts. By causing constant stimulation of the pituitary, it decreases pituitary secretion of gonadotropins luteinizing hormone (LH) and follicle stimulating hormone (FSH). Like other GnRH agonists, triptorelin may be used in the treatment of hormone-responsive cancers such as prostate cancer or breast cancer, precocious puberty, estrogen-dependent conditions (such as endometriosis or uterine fibroids), and in assisted reproduction. It is also used as therapy in cases of gender dysphoria. Triptorelin is marketed under the brand names Decapeptyl (Ipsen) and Diphereline and Gonapeptyl (Ferring Pharmaceuticals). In the United States, it is sold by Watson Pharmaceuticals as Trelstar. In Iran Triptorelin is marketed under the brand name Variopeptyl.

Raw Peptide Powder Tesamorelin

Product Name: Tesamorelin
Alias: Egrifta
CAS: 218949-48-5
MF: C221H366N72O67S
MW: 5135.9
Grade: Pharmaceutical Grade
Appearance: White Powder

Tesamorelin (INN) (trade name Egrifta) is a synthetic form of growth-hormone-releasing hormone (GHRH) which is used in the treatment of HIV-associated lipodystrophy. It is produced and developed by Theratechnologies, Inc. of Canada.

Tesamorelin is a synthetic peptide consisting of all 44 amino acids of human GHRH with the addition of a trans-3-hexenoic acid group.

Tesamorelin is used for Reducing excess stomach fat in certain HIV-infected patients.

Tesamorelin is a human growth hormone-releasing factor (GRF) analog. It works by stimulating the pituitary gland to release growth hormone (GH). This causes the breakdown of excess stomach fat.

Do Not Use Tesamorelin If:

you are allergic to any ingredient in tesamorelin or to mannitol
you are pregnant
you have cancer, an underactive pituitary gland, or a pituitary gland tumor
you have had your pituitary gland removed, pituitary gland surgery, radiation treatment of the head, or a head injury
Contact your doctor or health care provider right away if any of these apply to you.

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Before using tesamorelin:

Some medical conditions may interact with tesamorelin. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are planning to become pregnant or are breast-feeding
if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement
if you have allergies to medicines, foods, or other substances
if you have a history of cancer, noncancerous growths, or diabetes
if you have severe breathing problems (eg, respiratory failure); a serious illness caused by complications from surgery, injury, or trauma; or kidney or liver problems

Some MEDICINES MAY INTERACT with tesamorelin. Tell your health care provider if you are taking any other medicines, especially any of the following:

Anticonvulsants (eg, phenytoin), corticosteroids (eg, prednisone), cyclosporine, or sex hormones (eg, estradiol, testosterone) because the risk of their side effects may be increased by tesamorelin.

This may not be a complete list of all interactions that may occur. Ask your health care provider if tesamorelin may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How To Use Tesamorelin

Use tesamorelin as directed by your doctor. Check the label on the medicine for exact dosing instructions.

An extra patient leaflet is available with tesamorelin. Talk to your pharmacist if you have questions about this information.

Tesamorelin is usually given as an injection at your doctor's office, hospital, or clinic. If you will be using tesamorelin at home, a health care provider will teach you how to use it. Be sure you understand how to use tesamorelin. Follow the procedures you are taught when you use a dose. Contact your health care provider if you have any questions.

Do not use tesamorelin if it contains particles, is cloudy or discolored, or if the vial is cracked or damaged.

Use the proper technique taught to you by your doctor. Inject deep under the skin, NOT into a vein or muscle.

Be sure to rotate your injection site on the stomach area with each dose as directed. Do not inject tesamorelin into scar tissue, bruises, or the belly button.

Tesamorelin needs to be mixed before use. Follow how to mix as you were told by the doctor.

Do not prepare tesamorelin until you are ready to use it. After mixing, use tesamorelin right away and throw away any unused medicine. Do not store prepared doses for later use.

Keep this product, as well as syringes and needles, out of the reach of children and away from pets. Do not reuse needles, syringes, or other materials. Ask your health care provider how to dispose of these materials after use. Follow all local rules for disposal.

If you miss a dose of tesamorelin, use it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not use 2 doses at once.

Ask your health care provider any questions you may have about how to use tesamorelin.

Important safety information:

The safety of long-term use of tesamorelin is not known. Contact your doctor if your condition does not improve while you use tesamorelin.
Tesamorelin is not intended to manage weight loss.

Tesamorelin may raise your blood sugar. High blood sugar may make you feel confused, drowsy, or thirsty. It can also make you flush, breathe faster, or have a fruit-like breath odor. If these symptoms occur, tell your doctor right away.

Diabetes patients - Tesamorelin may affect your blood sugar. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.

LAB TESTS, including IGF-I and blood sugar levels, may be performed while you use tesamorelin. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Tesamorelin should not be used in CHILDREN; safety and effectiveness in children have not been confirmed.

PREGNANCY and BREAST-FEEDING: Do not use tesamorelin if you are pregnant. It may cause harm to the fetus. Avoid becoming pregnant while you are taking it. If you become pregnant, stop taking tesamorelin and contact your doctor right away. It is not known if this medicine is found in breast milk. Mothers infected with HIV should not breast-feed. There is a risk of passing the HIV infection or tesamorelin to the baby.

Possible Side Effects Of Tesamorelin

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Nausea; night sweats; stomach upset; trouble sleeping; vomiting.

Seek medical attention right away if any of these SEVERE side effects occur:
Severe allergic reactions (rash; flushing; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, throat, or tongue); arm, joint, leg, or muscle pain; burning, numbness, or tingling of the skin; decreased sense of touch; fainting or faintness; fast or irregular heartbeat; mental or mood changes (eg, depression); muscle or joint soreness or stiffness; numbness, pain, or weakness in your wrist, hand, or fingers; redness, swelling, itching, pain, irritation, rash, bleeding, or bruising at the injection site; shortness of breath or trouble breathing; swelling of the hands, ankles, or feet; symptoms of high blood sugar (eg, increased thirst, hunger, or urination; confusion; drowsiness; flushing; rapid breathing; fruit-like breath odor).

Raw Peptide Powder TB500

Product Name: TB500
Alias: Thymosin Beta 4 Acetate
CAS: 77591-33-4
MF: C212H350N56O78S
MW: 4963.50
Grade: Pharmaceutical Grade
Appearance: White Powder
Specification: 2mg/vial

TB500 Is Part Of Thymosin Beta 4 Acetate

TB-500 is a synthetic fraction of the protein thymosin beta-4, which is present in virtually all human and animal cells. Thymosin beta-4 is a very large molecule. In fact, it is so large that it cannot fit entirely into the receptor. Different sections of the molecule have different activities. TB-500 is the part of thymosin beta-4 hormone which promotes the most useful effects (overall healing, repair, new blood and muscle cells). For medical applications it is more practical to use the TB-500 instead of the entire Thymosin Beta-4 protein.

Promote Healing

The main purpose of TB500 is to promote healing. It also promotes creation of new blood and muscle cells. The healing effects of TB-500 have been observed in tendons, ligaments, muscle, skin, heart, and the eyes. Thymosin beta-4 is naturally produced in higher concentration where tissue has been damaged.

TB-500 is specifically designed to help deal with injured athletes and bodybuilders,it is an injectable peptide drug which can be used to promote healing, enhance range of motion in cases of injury, or reduce pain in case of injury by reducing inflammation.This peptide is also a very potent anti-inflamatory agent.

TB500 is a synthetic peptide that has been directly linked to recovery as it is plays a vital role in building new blood vessels, new small muscle tissue fibers, cell migration and blood cell reproduction. If you are an injured athlete, all of these properties are something that becomes very desirable when looking to speed up the recovery process.

Dosage And Usage

TB500 is distributed as a lyophilized powder that should be kept out of the light and in a cool dry place.  Reconstitution is done with bacteriostatic water or sodium chloride meant for injection.  Doses range from 2-2.5mg twice weekly for 4-6 weeks (some user have reported success in dosing higher up to 8mg a week but how much more effective this is yet to be seen) .  Beyond that, one to two monthly injections of 2-2.5mg of TB500 can be further utilized to maintain rapid recovery and flexibility in strained areas.

For optimal recovery, a combination of TB500 with MK-2866 (Ostarine) should be used.  This combination allows the healing benefits of SARMS and peptides to delivery maximum results.

Side Effects

The positive attributes of TB500 include blood vessel and cell differentiation, growth of new blood cells from pre-existing vessels in dermal tissue, decreased inflammation and increase in flexibility.  The flu like symptoms or lethargy/head rush associated with most peptides does not seem to be widely reported with TB500.  Everybody is different, so always follow the suggested dosing protocols and practice sterile injection techniques.  This will cut down on environmental side effects associated with injections.

Raw Peptide Powder Sermorelin

Product Name: Sermorelin
Alias: Somatoliberin,Sermorelinum,Sermorelina,Sermoreline,GRF 1-29
CAS: 86168-78-7
MF: C149H246N44O42S
MW: 3357.96
Purity: 98.0%min
Grade: Pharmaceutical Grade
Appearance: White Powder
Specification: 2mg/vial

GRF 1-29

Sermorelin is actually known to us by the name GRF (1-29).  The original GFR (1-29) is, in fact, the root of the HGH molecule and that remaining peptide containing the first 29 amino acids is actually what is responsible for stimulating pituitary response.  The name Sermorelin is the prescription drug name and this alone is why it is so widely prescribed by hormone replacement therapy clinics (HRT).

In fact, anti-aging and hormone replacement clinics have been prescribing GRF 1-29 for years because it works as a clean GHRH.  The problem for the bodybuilder or athlete is that it has a very short half-life of about ten minutes.  This becomes an unattractive feature when compared to the half-life of MOD GRF (1-29) (CJC 1295 without DAC), which comes in around 30 minutes.  Despite its short window, it does bind quite effectively to the pituitary receptors.  The other main down side associated with its very short half life is that it is quickly broken down by blood enzymes within minutes.  This is why a GHRH peptide with a half life of 30 minutes or longer is desirable, since it will survive the blood enzyme death and allow it to circulate the body looking for hormone receptors to bind to.

HRT Function

So, why would bodybuilders or athletes want to utilize Sermorelin over other peptides that have longer half lives like MOD GRF (1-29) or CJC 1295 with DAC?  To put it simply, you could easily work this into a multi-dosing protocol along with you other long acting GHRH's and GHRP's. Let's look at Sermorelin's known positive effects like: increased lean body mass, reduced fat, increased strength, improved recovery, better sleep, strengthenining of the heart, enhancing of the immune system and increases IGF-1 production.  Yes, while the ability of Sermorelin to act is short, it still promotes all of these factors stated above. Not to mention it also has the ability to increase protein synthesis, promote growth of all internal organs with the exception of the brain and promote and increase in liver glucogenesis. Despite its tiny half life, Sermorelin's ability to increase IGF-1 in the blood stream will only further increase the function of the metabolism and the growth of new cells in muscles, bones and organs. Sermorelin is heavily pushed by HRT clinics and is often referred to as the anti-aging peptide since it is very good at reversing some of the effects of aging in adults.  The fact that doctors can legally prescribe this peptide helps HRT clinics further their legitimacy and also offer a viable and more cost effective solution to prescribing exogenous HGH.

Dosage And Usage

Sermorelin, along with the other peptides you will use, comes as a delicate lyophilized powder that should be kept out of the light and in a cool dry place.  Reconstitution is done with bacteriostatic water (BC water) or sodium chloride meant for injection.  Injections can be administered one hour before workout at a dose of 200mcg-300mcg.  Normally, Sermorelin injections are taken before bed at around 300mcgs. Of course, as with any GHRH, you will want to use this peptide alongside a GHRP like GHRP-2 or Ipamorelin for maximum release of growth hormone stores.  Ideally, though user could still benefit from using a GHRH like CJC 1295 with DAC and a GHRP like Ipamorelin throughout the day and then utilize Sermorelin as a pre-bed timed dose.  Do not discount Sermorelin as simply an anti-aging peptide.  It can still help promote the growth of lean body mass and increase the availability of IGF-1 in the blood stream.

Side Effects

Sermorelin is pretty mild in terms of side effects, but, like most peptides, it has the ability to bring on head rush, flush feeling, some swelling at injection site, dizziness, and nausea.  I could not find any cases where prolactin or cortisol levels were elevated by the use of Sermorelin. As always, listen to your body and follow a dosing protocol that is in tune with you goals.

Raw Peptide Powder Selank

Product Name: Selank
Synonyms: Selanc
Molar Mass: 751.8
Purity: 98.71%
Grade: Pharmaceutical Grade
Appearance: White Powder
Specification: 5mg/vial

Selank or selanc is a synthetic heptapeptide analog of the endogenous tetrapeptide tuftsin, with the sequence Thr-Lys-Pro-Arg-Pro-Gly-Pro. This synthetic variant of immunomodulatory tetrapeptide tuftsin possesses anxiolytic properties because of its mimic nature. Among this peptide's positive characteristics, are its ability to induce serotonin's metabolic processes and affect the concentration of specific monoamine neurotransmitters. Some scientists believe that Selank possesses such modulatory feature as influencing expression of brain-derived neurotropic factor.

Neuropeptide Selank is a synthetic derivative of the human body's naturally produced tetrapeptide Tuftsin. It is a hexapeptide whith a wide range of uses. Selank is used as an anxiolytic in the therapy of anxiety and phobic disorders, including generalized anxiety. Its action is similar to that of mild benzodiazepins but without the sedative effects. As a selective anxiolytic with a nootropic component, Selank can be used as treatment of depression, fear and general anxiety. It also reduces phsychic tension. This neuropeptide has passed all phases of clinical trials and is now being prepared for registration and mass production.

Selank is closely related to Semax, a hexapeptide previously invented by the same institute. Some consider Selank to be a more efficient alternative to Semax.

Selank As A Nootropic

Recreationally Selank is used to improve one's ability to focus and concentrate, reduce mental fatigue, increase mental sharpness and increase memory and learning capacity. The first noticeable effect is usually stabilization of mood and general feeling of well-being.

Selank As An Antiviral Agent

Selank neuropeptide also expresses immunomodulatory effects. In 2009 a study by F. Ershov et all. has evaluated antiviral properties of Selank both in vitro and in vivo against the influenza virus strain A/Aichi 2/68 (H3N2). The pronounced antiviral effect of Selank was detected in both systems. The highest efficiency - completely supressed viral reproduction was shown when Selank was added to the cell culture 24 hours before inoculation.

Selank Effects

Improvement of learning and memory processes (reference, reference)
Increased sensory attention
Increased curiosity
Increased mental clarity
Restoration of balance of serotonergic and noradrenergic brain system activity (reference)
Anti-anxiety - inhibition of anxiety (reference)
Antiviral activity with no negative effects (reference)
Psychostimulant, anti-asthenic - increased mental energy (reference)
Stabilization of mood and overall feeling of wellbeing
Reversal of anhedonia (restoring the feeling of pleasure)
Potential restoration of catecholaminergic system functions after damage due to drug abuse reference

Raw Peptide Powder PT141

Product Name: PT141
Alias: Bremelanotide,Brmelanotice,BreMelanotide Acetate
CAS: 189691-06-3
MF: C50H69N15O10
MW: 1040.17736
Purity: 99%
Grade: Pharmceutical Grade
Appearance: White Powder

Developed From Melanotan II

Bremelanotide or PT-141, a research chemical and peptide, belongs to the classification known as melanocyte stimulating hormones (MSH).  It is a hexapeptide analog of alpha-MSH, and was originally developed from the MSH Melanotan II, a peptide agent that was reviewed in trials for sunless tanning but, unexpectedly, resulted in sexual arousal and sexual spontaneous erections in nine of ten test subjects.

Bremelanotide is a compound under drug as a treatment for female and male sexual dysfunction, hemorrhagic shock and reperfusion injury. 

Treatment Of Sexual Dysfunction

Bremelanotide or PT-141 is the generic term for a new research peptide for use in helping improve sexual dysfunction in men (erectile dysfunction or impotence) as well as helping improve sexual dysfunction in women (sexual arousal disorder).

PT-141 is a potential remedy for the treatment of sexual dysfunction; specifically, male erectile dysfunction.Bremelanotide, PT-141 does not act on the vascular system like the former compounds but it is known and has been shown to help increase sexual activity in both male and female mammals. Bremelanotide PT-141 allegedly works by activating melanocortin receptors in the brain, therefore helping increase ones sexual stimulation.

Bremelanotide is a novel treatment that could potentially change the face of treating sexual disorders, not only because of its effectiveness due to a unique mode of action, but also due to its safety and the fact it works synergistically with other ED/SAD treatments.

Bremelanotide is effective in its potential to treat sexual desire disorders as well as disorders that affect physical arousal. Bremelanotide induces lordosis in animal subjects, a sign of physical preparation for copulation. In males, it does not stimulate the vascular aspect of the penis, but instead acts to stimulate the central nervous system primarily via dopamine receptor activity to increase sexual desire and also demonstrates functionality in treating purely physical manifestations of ED/SAD, likely through improved signalling.

Co-Administration Pf PT-141 And Sildenafil

Bremelanotide also offers potential as a low-dose concurrent treatment with low-dose sildenafil.

The erectile response induced by co-administration of PT-141 and sildenafil was significantly greater than the response elicited by administration of sildenafil alone. Co-administration of PT-141 and sildenafil was safe and well-tolerated and did not result in new adverse events or adverse events that were increased in frequency or severity compared with monotherapy. Co-administration of intranasal PT-141 and a phosphodiesterase type 5 inhibitor may constitute a treatment alternative for patients in whom higher doses of a single therapy are not effective or well tolerated.

Raw Peptide Powder Pentadecapeptide BPC 157

Product Name: Pentadecapeptide BPC 157
Alias: Booly Protection Compound 15
CAS: 137525-51-0
MF: C62H98N16O22
MW: 1419.53552
Purity: 99%
Grade: Pharmaceutical Grade
Appearance: White Powder
Specification: 2mg/vial

Pentadecapeptide BPC 157, composed of 15 amino acids, is a partial sequence of body protection compound (BPC) that is discovered in and isolated from human gastric juice. Experimentally it has been demonstrated to accelerate the healing of many different wounds, including transected rat Achilles tendon. This study was designed to investigate the potential mechanism of BPC 157 to enhance healing of injured tendon. The outgrowth of tendon fibroblasts from tendon explants cultured with or without BPC 157 was examined. Results showed that BPC 157 significantly accelerated the outgrowth of tendon explants. Cell proliferation of cultured tendon fibroblasts derived from rat Achilles tendon was not directly affected by BPC 157 as evaluated by MTT assay. However, the survival of BPC 157-treated cells was significantly increased under the H(2)O(2) stress. BPC 157 markedly increased the in vitro migration of tendon fibroblasts in a dose-dependent manner as revealed by transwell filter migration assay. BPC 157 also dose dependently accelerated the spreading of tendon fibroblasts on culture dishes. The F-actin formation as detected by FITC-phalloidin staining was induced in BPC 157-treated fibroblasts. The protein expression and activation of FAK and paxillin were determined by Western blot analysis, and the phosphorylation levels of both FAK and paxillin were dose dependently increased by BPC 157 while the total amounts of protein was unaltered. In conclusion, BPC 157 promotes the ex vivo outgrowth of tendon fibroblasts from tendon explants, cell survival under stress, and the in vitro migration of tendon fibroblasts, which is likely mediated by the activation of the FAK-paxillin pathway.

BPC 157 has a strong anti-inflammatory activity in both acute and chronic inflammation models. In fact, preliminary results in clinical trials suggest that BPC 157 may become an important therapeutic tool for the treatment of inflammatory bowel disease. BPC 157 was shown to accelerate wound healing and to have a marked angiogenic effect. In addition, it significantly facilitates the healing of bone fracture in rats. This peptide also exhibits an osteogenic effect significantly improving the healing of segmental bone defect. BPC 157 accelerates the healing of transected rat Achilles tendon and transected rat quadriceps muscle.

Raw Peptide Powder PEG-MGF

Product Name: Pegylated Mechano Growth Factor,PEG MGF
Molecular Formula: C121H200N42O39
Purity (HPLC): 98.0%
Packing: 2mg/vial
Grade: Pharmarceutical Grade
Appearance: White powder

Longer half life of MGF

PEGylation is the act of attaching a Polyethylene glycol (PEG) structure to another larger molecule (in this case, MGF). The PEG acts as a protective coating and the theory here is that this will allow the MGF to be carried through the blood stream without being broken down.

MGF that's pegylated, which means it has the addition of Polyethylene glycol - a non toxic additive that increased the half life of MGF from minutes to hours.  This means its uses and versatility make it a tremendous addition to a bodybuilders arsenal.  I have found it most effective, as its effects are systematic, that means they have a whole body effect wherever muscle has been damaged or is diseased.

PEG MGF Benefits

When your muscle is damaged, your body releases a pulse of an MGF splice variant as I outlined above, followed by a less anabolic longer acting version from the liver.  Therefore, it seems a waste to inject MGF at this time as you will just blunt your body's own release, your not enhancing it.  So using PEG MGF on non workout days is actually the best route.  Since the muscle has been damaged, there are plenty of receptors for MGF, and the effects are systematic.  All muscles will be aided in recovery through increased nitrogen retention, protein turnover, and satellite cell activation.  Recovery is just going to sky rocket.  Doing this means you're increasing the length of your body's own mechanism for muscle repair and growth, and you're opening up the anabolic window.

When you are working out, you are breaking muscles down and the real growth happens when the muscle heals and cells are able to grow and increase in size.  This is where PEG MGF can be utilized as an incredible recovery tool.  PEG MGF can be ran as a standalone peptide post workout, but it's especially useful on recovery days.  By injecting 200mcg bilaterally (subcutaneously or intramuscularly) PEG MGF will bind to receptors and actually help recover damaged muscle tissue better than IGF-1. PEG MGF has also shown to signal satellite cells close to the damaged muscle tissue to grow just as if they were a part of the damaged tissue cells.  This means that damaged cells are going to grow larger and faster, but also it is going to grow cells near the damaged tissue.  In simple terms, this means you're creating new muscle tissue while recovering the already-existing muscles.  This is extremely helpful, considering that as you get older the ability to proliferate satellite cell regeneration decreases drastically.  This leads to age related muscle loss, as you aren't able to create new muscle cells.  This is where MGF comes in!  Mechano growth factor directly increases the availability of muscle cell production; therefore, recovery times from damaged muscle tissue are going to decrease and muscle size is, in turn, increased.

Doses and Usage

Using PEG MGF on cycle or off cycle, you are going to experience recovery that is far superior to any generic peptide available.  Just like normal peptides, remember that PEG MGF comes in the form of a white delicate powder that needs to be reconstituted with bacteriostatic water and kept in the refrigerator.

PEG MGF does not need to be systematically administered because of its long half-life (several days).  It will circulate your body binding to the receptors where muscle tissue damage has taken place.  Administration should be timed post workout or on recovery days when you plan on resting.  Since mechano growth factor is a variant of IGF-1, you do not want to use MGF pre-workout because it will have to fight for position with IGF-1 as they both try to bind to the same receptor.  IGF-1 has a much stronger affinity to bind then MGF.

Rest days are the best way to get the most use out of PEG MGF, as you will have lower level of IGF-1 and the long lasting PEG MGF will have the ability to run the course of the body while you focus on recovery. I have personally ran PEG MGF and administered into the quad regions after very long sessions where my quads were ripped to shreds.  The recovery time and muscle growth in those areas was noticed after one week of use.  Duly noted was the recovery time after a 100+ mile ride. On the recovery day, I administered 200mcg of PEG MGF and rested.  The following day muscles felt recovered and soreness was not present for the next training ride.

An insulin syringe needs to be used to inject subcutaneously or intramuscularly with a dose around 200-400mcg.  Bilateral dosing can be used, but a single site administration will work just as well.

Raw Peptide Powder Oxytocin

Product Name: Oxytocin
Alias: Atonin,,Orasthin,Oxytocinum,Partocon,Pitocin,Piton,Pitupartin,Utedrin
CAS: 50-56-6
EINECS: 200-048-4
MF: C43H66N12O12S2
MW: 1007.19
Purity: 98.0%min
Grade: Pharmaceutical Grade
Appearance: White Powder

Usage: For induction of labor, postpartum oxytocin, and abortion due to uterine atony or retraction caused by the bad uterus bleeding; understand the placental function reserve (oxytocin challenge test); nasal drops can promote milk ejection.

Oxytocin (Oxt) is a mammalian neurohypophysial hormone. Produced by the hypothalamus and stored and secreted by the posterior pituitary gland, oxytocin acts primarily as a neuromodulator in the brain.
Oxytocin plays an important role in the neuroanatomy of intimacy, specifically in sexual reproduction of both sexes, in particular during and after childbirth; its name, meaning "swift childbirth", comes from Greek, oksys "swift" and , tokos "birth". It is released in large amounts after distension of the cervix and uterus during labor, facilitating birth, maternal bonding, and, after stimulation of the nipples, lactation. Both childbirth and milk ejection result from positive feedback mechanisms.

Application

Injected oxytocin analogues are used for labor induction and to support labor in case of difficult parturition. It has largely replaced ergometrine as the principal agent to increase uterine tone in acute postpartum hemorrhage. Oxytocin is also used in veterinary medicine to facilitate birth and to stimulate milk release. The tocolyticagent atosiban (Tractocile) acts as an antagonist of oxytocin receptors; this drug is registered in many countries to suppress premature labor between 24 and 33 weeks of gestation. It has fewer side effects than drugs previously used for this purpose (ritodrine, salbutamol, and terbutaline).

Usage And Dosage

Odinopoeia or oxytocin intravenous drip, once the 2.5 - 5 units, with Sodium Chloride Injection diluted to each 1ml contains 0.01 units. Intravenous drip of the beginning of every minute of not more than 0.001 to 0.002 units, each 15 - 30 minutes increased 0.001 to 0.002 units, to achieve the contractions and normal childbirth is similar, the fastest per minute of not more than 0.02 units, usually 0.002 to 0.005 units per minute.

Control postpartum hemorrhage per minute intravenous drip of 0.02 - 0.04 units, expulsion of the placenta after intramuscular injection of 5 to 10 units.
Lactogenic just before a 2 - 3 minutes, with nasal drops a 3 drop, drop into one side or both sides of the nostril.

Preparation and specification : oxytocin injection (1) 0.5ml:2.5 units (2) 1ml:5 (3) 1ml units 10 units;

Oxytocin nasal drops 1ml:40 units. The induction of labor or prenatal uterine atony: in 2.5-5 units in 500ml 5% glucose for intravenous drip slowly (10-30 drops / minute), maximum time 20 units. (2). Prevention of postpartum hemorrhage: intramuscular injection of 5-10 on each unit, or 5% glucose solution for intravenous drip.

The main contraindication, heart disease, a caesarean history and more than three fetal maternal disable.

Raw Peptide Powder MGF

Product Name: MGF
Alias: Mechano Growth Factor
MF: C121H200N42O39
MW: 2888.16
Purity: 99%
Grade: Pharmarceutical Grade
Appearance: White Powder
Specification: 2mg/vial

2 Kinds Of MGF Splice Variants Of IGF

Mechano Growth Factor (MGF) also known as IGF-1Ec is a growth factor/repair factor that is derived from exercised or damaged muscle tissue.  It's called MGF as IGF-IEa is a bit of a mouthful and harder to identify amongst the other IGF variants.

IGF-1Ec: This is the first phase release igf splice variant and it appears to stimulate satellite cells into activation, This is the closest variant to synthetic MGF.When mechanical overload is introduced to a muscle (as by weight training), the IGF-1 gene released and is differentially spliced during the bodies response. Initially, it it is spliced to produce predominantly IGF-1Ec (called the MGF splice variant of IGF-1). This early splicing stimulates satellite cells into activation. Which in turn allows the activation of extra undamaged nuclei to grow new muscle fiber and tissue. The appearance of MGF also initiates the upregulation of new protein synthesis.

IGF-1Ea: After this initial splicing of IGF-1 into MGF, production then switches towards producing a systemic release of IGF-1Ea from the liver, which also upregulates protein synthesis as well. It is the secondary release of igf from the liver, and its far less anabolic and shorter acting.

The expression of IGF-1 splice variants, over the course of the healing and regrowth phase of muscle repair is thought to be the primary anabolic mechanism by which the body produces new muscle. MGF is available as an injectable peptide, and it has been anecdotally shown that injecting it will cause a response in the area resulting in localized muscle growth.

MGF Benefits

MGF is a splice variant of the IGF gene which increases stem cell count in the muscle and allows for muscle fibers to fuse and mature. This is a process required for growth of adult muscle. Natural MGF is made locally and does not travel into the bloodstream. Synthetic MGF is water based and when administered intramuscularly, travels into the bloodstream. MGF is only stable in the blood stream for only a few minutes.

In bodybuilding this drug is used to accelerate muscle growth. Other effects of the drug include decrease of fat mass of the body, endurance increase, improvement of immune defenceand skin, bone strengthening, lowering of cholesterol level, accelerated recovery. Those who administered MGF declared that they experienced no side effects, which frequently occur with the use of other drugs for gaining body mass.

Muscle Repair Factor

When you train, what happens to your muscles is they break down, the cells are damaged, muscle tissue needs to be repaired and your body produces 2 forms of MGF splice variant. The first initial release of the above mentioned number 1 variant from the liver helps muscle cell recovery, if there is no MGF then muscle cells die.

As muscle is a post-mitotic tissue and as such cell replacement is not a means of tissue repair, if the cells are not repaired they die and your muscles get smaller and weaker.  In muscle tissue, the pool of these stem cells is apparently replenished by the action of MGF, which is produced as a pulse following damage.

Now, with synthetic injections of MGF you can increase the pulse and so speed up recovery, and increase the muscle tissue cells by stimulating satellite cells into full maturity. In terms of dosages, 200mcg bi-laterally is the very best choice of dosing in muscles trained.