PEG-MGF
Alias: PEG-Suc-YQPPSTNKNTKSQ(d)R(d)RKGSTFEEHK-NH2; PEG-Suc-Tyr-Gln-PRO-PRO-Ser-Thr-Asn-Thr-Lys-Ser-Gln-D-Arg-Lys-Gly-Ser-Thr-Phe-Glu-Glu-His-Lys-NH2
M.F.: C121H200N42O39
Purity (HPLC): 98.0%
Single Impurity(HPLC): ≤0.5%0.5%0.5%
Amino Acid Composition: ±10% of theoreticaloreticaloretical
Peptide Content(N%): ≥80.0%0.0%0.0%
Water Content(Karl Fischer): ≤8.0%;8.0%8.0%
Acetate Content(HPLC):≤10.0%0.0%0.0%
Specific Rotation: (20/D) -55.0~-65.0°(c=1 1%HAc)%HAc)%HAc)
MS(ESI): Consistent
Mass Balance: 95.0~105.0%
Bacterial Endotoxins: ≤5 EU/mgU/mgU/mg
Packing: 2mg/vial,10vials/kit
Appearance: White powder
Usage: Pharmaceutical intermediates.
Description:
PEG-MGF Useful for: Site-enhancement and systematic purposes through increased lean muscle and fat loss
PEG-MGF Possible Benefits: PEG-MGF stimulates muscle growth (hypertrophy); increases the rate of muscle growth from training; rapid repair of existing muscle cells; increases in the number of muscle cells (hyperplasia); reduces protein breakdown; increases the rate & extent of muscle repair after injurynjurynjury
Consumption Method 1: Localized injection directly into the muscle immediately post-workout
Consumption Method 2: Subcutaneous injection into layer of fat
Preparation for Injection: Add 1ml (100 IU) of sterile solution to the PEG-MGF vial. Every 200mcg is then equal to 0.1ml (10 IU).
PEG-MGF Dosage 1: 200mcg (10 IU) of PEG-MGF split bilaterally between muscles just trained i.e. 100mcg left side, 100mcg right side
PEG-MGF Dosage 2: 200mcg (10 IU) of PEG-MGF is to be injected into abdominal fat
PEG-MGF Doses per Vial: 10 x 200mcg doses (10 doses per vial)

Description
It was first discovered in the muscle by Goldspink, et al. In human muscle, a 49-base insert changes the reading frame in mechano factor (MGF) as compared to I-GF-1.
When mechanical overload is introduced to a muscle (as by weight training), the I-GF-1 gene released and is differentially spliced during the bodies response. Initially, it it is spliced to produce predominantly I-GF-1Ec (called the MGF splice variant of I-GF-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. After this initial splicing of I-GF-1 into MGF, production then switches towards producing a systemic release of I-GF-1Ea from the liver, which also upregulates protein synthesis as well. The expression of I-GF-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

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