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BPC 157 - 10mg Magnus

1 vial/10mg

Product name: BPC 157 - 10mg

Substance: Peptide

Manufacturer: Magnus Pharmaceuticals

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Read The Spec Sheet Below Before You Buy BPC - 157:

Unit Size

10 mg/vial

Unit Quantity

1 Vial

CAS NO.

137525-51-0

Synonyms

Body Protection Compound-157 L-Valine, glycyl-L-alpha-glutamyl-L-prolyl-L-prolyl-L-prolylglycyl-L-lysylL-prolyl-L-alanyl-L-alpha-aspartyl-L-alpha-aspartyl-L-alanylglycyl-Lleucyl-

Molecular Formula

C62H98N16O22

Molecular Weight

1419.53552 g/mol

Sequence

Appearance

White Powder

Purity

98.46%

Identity (ESI-MS)

1420.50

Source

Chemical Synthesis

Storage

Lyophilized PT-141 is stable at room temperature for 90 days,however it should be stored in a freezer below -8C for any extended period of time. After reconstituting PT-141 should be refrigerated at temperatures not to exceed 36 F.

BPC-157

BPC-157 (Body Protection Compound-157) is a pentadecapeptide made up of 15 amino acids. The amino acids sequence in BPC-157 is similar to a portion of the human BPC amino acid sequence. Human BPC is found in the gastric juice. Experiments have shown that BPC-157 enhances the healing of wounds, including tendons wounds such as transected Achilles tendons of rats. The aim of this study was to investigate the probable mechanism that BPC-157 utilizes to accelerate the healing process in an injured tendon. The study used two group of tendon explants of which one group was cultured in a BPC-157 containing medium while the other group was cultured in a medium lacking BPC-157. These cultures were thereafter examined for tendon fibroblasts outgrowths. Such outgrowths indicated tendon regeneration.The results revealed that the explants’ outgrowth was significantly accelerated in the culture containing BPC-157 as compared to the culture lacking BPC-157. Also, a MTT assay did show that BPC-157 does not directly affect cellular proliferation in a culture of rat-derived Achilles tendon. However, results also showed that BPC-157 significantly increased the survival of cells under oxidative stress. Furthermore, the Transwell filter migration assay showed that BPC-157 significantly increased in-vitro fibroblast migration in a dose-dependent fashion. Moreover, BPC-157 accelerated the dispersal of the fibroblasts in culture dishes in a dose-dependent manner.

Additionally, FITC-phalloidin staining was able to demonstrate that BPC-157 induces F-actin formation in fibroblasts. Likewise, Western blot analysis was able to detect the production and activation of paxillin and FAK proteins. The western blot analysis also showed that BPC-157 increases the extent of phosphorylation of paxillin and FAK proteins without affecting the amounts produced.

Thus, it can be concluded that BPC-157 enhances the ex-vivo growth and in-vitro cellular migration of fibroblasts derived from rat tendon explants. Moreover, BPC-157 also increases the probability of a cell surviving under oxidative stress. These actions of BPC-157 are probably mediated by the activation (through phosphoryl) of the proteinic FAK-paxillin pathway.

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