BPC157 main information：
Protuct Name: BPC157
Alias: Booly Protection Compound 15, Pentadecapeptide, BPC 157
Sequence: Gly-Glu-Pro-Pro-Pro-Gly- Lys-Pro-Ala-Asp-Asp-Ala-Gly-Leu-Val
Specification: 1mg/vial 10vials/kit
Min order: 1kit
Appearance: White Lyophilized Powder
Grade Standard: Pharmacy Grade
Place of Origin: China (Mainland)
Method of Analysis: HPLC
Storage: Lyophilized peptides although stable at room temperature for 3 months, should be stored desiccated below -18° C. Upon reconstitution of the peptide it should be stored at 4° C between 2-21 days and for future use below -18° C.
The benifits of the BPC157
Studies showed TB-500 is a potent, naturally occurring wound repair factor with anti-inflammatory properties. Tß4 is different from other repair factors, such as growth factors, in that it promotes endothelial and keratinocyte migration. It also does not bind to the extracellular matrix and has a very low molecular weight meaning it can travel relatively long distances through tissues. One of TB-500 key mechanisms of action is its ability to regulate the cell-building protein, Actin, a vital component of cell structure and movement. Of the thousands of proteins present in cells, actin represents up to 10% of the total proteins which therefore plays a major role in the genetic makeup of the cell.
BPC157 has a strong antiinflammatory activity in both acute and chronic inflammation models. In fact, preliminary results in clinical trials suggest that BPC157 may become an important therapeutic tool for the treatment of inflammatory bowel disease. BPC157 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.
FITCphalloidin staining was able to demonstrate that BPC157 induces Factin 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 BPC157 increases the extent of phosphorylation of paxillin and FAK proteins without affecting the amounts produced.
CJC-1295 without DAC
CJC-1295 with DAC
HGH Fragment 176-191
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