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Sema 10mg — GLP-1 analogue peptide RUO — lyophilized powder — Research Use Only.

Original price was: $149.99.Current price is: $74.99.

Semaglutide is a synthetic peptide analogue of human GLP-1 supplied as a lyophilized powder for laboratory investigations in peptide chemistry and receptor-signaling research. Each vial contains 10 mg research-grade material with HPLC verification (see COA for lot-specific data). For laboratory research use only; not for human or veterinary use.

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SKU: SemaGlutide10mg Category: Tags: , , , Brand:

Description

Semaglutide 10 mg (GLP-1 analogue) for laboratory research. Lyophilized powder, HPLC-verified. RUO—Not for human or veterinary use.

RUO Disclaimer: This material is supplied exclusively for laboratory research by qualified professionals. It is not a drug, supplement, diagnostic, or cosmetic, and is not intended to diagnose, treat, cure, or prevent any disease. No dosing, safety, or efficacy claims are made.

Semaglutide Peptide 10mg

Peptides Semaglutide

What is Semaglutide?

Semaglutide is a glucagon-like peptide-1 (GLP-1) receptor agonist that has been investigated for its effects on body weight and cardiometabolic parameters in controlled research settings. In multiple studies utilizing once-weekly subcutaneous administration at a 2.4 mg dose, semaglutide consistently induced substantial reductions in body weight under experimental conditions. For example, in the STEP 5 investigation, which spanned 104 weeks, semaglutide treated subjects exhibited a mean body weight reduction of 15.2%, compared to 2.6% in control groups (Garvey et al., 2022). Similar effects were observed in the STEP 1 and STEP 3 trials, where mean body weight reductions of 14.9% and 16.0%, respectively, were reported after 68 weeks of semaglutide administration (Bergmann et al., 2023).

Semaglutide has also been associated with changes in cardiovascular endpoints in long duration studies. In a research protocol spanning a mean of 39.8 months and involving subjects with preexisting cardiovascular conditions and elevated body mass, semaglutide 2.4 mg administered weekly was associated with a reduced incidence of composite cardiovascular outcomes, including death from cardiovascular causes, nonfatal myocardial infarction, and nonfatal stroke (Lincoff et al., 2023). An earlier trial using 0.5 mg and 1.0 mg doses similarly reported a statistically significant reduction in the rate of first occurrence of cardiovascular death, nonfatal myocardial infarction, or nonfatal stroke in subjects with type 2 diabetes treated with semaglutide relative to placebo (Marso et al., 2016).

References

Bergmann, N. C., Davies, M. J., Lingvay, I., & Knop, F. K. (2023). Semaglutide for the treatment of overweight and obesity: A review. Diabetes, Obesity and Metabolism, 25(1), 18–35. https://doi.org/10.1111/dom.14863

Garvey, W. T., Batterham, R. L., Bhatta, M., Buscemi, S., Christensen, L. N., Frias, J. P., … & Wharton, S. (2022). Two-year effects of semaglutide in adults with overweight or obesity: the STEP 5 trial. Nature Medicine, 28, 2083–2091. https://doi.org/10.1038/s41591-022-02026-4

Lincoff, A. M., Brown-Frandsen, K., Colhoun, H. M., Deanfield, J., Emerson, S. S., Esbjerg, S., … & Ryan, D. H. (2023). Semaglutide and cardiovascular outcomes in obesity without diabetes. New England Journal of Medicine, 389(24), 2221–2232.
https://doi.org/10.1056/NEJMoa2307563

Wilding, J. P. H., Batterham, R. L., Calanna, S., Davies, M., Van Gaal, L. F., Lingvay, I., … & Kushner, R. F. (2021). Once-weekly semaglutide in adults with overweight or obesity. New
England Journal of Medicine, 384(11), 989–1002.
https://doi.org/10.1056/NEJMoa2032183

Marso, S. P., Bain, S. C., Consoli, A., Eliaschewitz, F. G., Jódar, E., Leiter, L. A., … & Vilsbøll, T. (2016). Semaglutide and cardiovascular outcomes in patients with type 2 diabetes. New England Journal of Medicine, 375(19), 1834–1844.
https://doi.org/10.1056/NEJMoa1607141

 

 

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