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SS-31 (Elamipretide) is a cell-permeable tetrapeptide that selectively targets cardiolipin on the inner mitochondrial membrane, preventing cytochrome c peroxidase activity and restoring electron transport chain function. A primary tool for mitochondrial bioenergetics and anti-aging research.
SS-31 (Elamipretide) is a cell-permeable tetrapeptide that selectively targets cardiolipin on the inner mitochondrial membrane, preventing cytochrome c peroxidase activity and restoring electron transport chain function. A primary tool for mitochondrial bioenergetics and anti-aging research.
Sermorelin Acetate is a 29-amino acid GHRH fragment that selectively stimulates pituitary somatotroph cells to release natural, pulsatile growth hormone. Its brief 11-15 minute half-life enforces physiological GH rhythms without receptor downregulation, making this ideal for evaluating endogenous GH axis function.
Melatonin is a fundamental circadian hormone that activates MT1 and MT2 receptors in the suprachiasmatic nucleus to regulate sleep-wake cycles and phase-shift circadian rhythms. Additionally, it acts as a direct free radical scavenger without requiring enzymatic catalysis.
LL37 for research use.
GnRH stimulator for hypothalamic-pituitary-gonadal axis research. Study fertility and reproductive endocrinology.
Ipamorelin is a third-generation selective ghrelin receptor agonist pentapeptide that triggers consistent growth hormone release without activating ACTH, prolactin, or cortisol pathways. Its 2-hour half-life produces a clean physiological GH pulse ideal for recovery and body composition research.
HGH 191AA (Somatropin) is recombinant human growth hormone with the exact 191-amino acid sequence produced by the pituitary. It directly triggers lipolysis and indirectly drives systemic IGF-1 elevation for full-scale tissue regeneration, muscle growth, and metabolic optimization.
Hexarelin is the most potent synthetic GHRP hexapeptide, acting as a high-affinity GHS-R1a agonist that produces the largest GH spike among all secretagogues. Uniquely, it also binds the CD36 receptor for cardioprotective signaling, positioning it as a dual-purpose tool for GH release and myocardial repair research.
HCG (Human Chorionic Gonadotropin) is a highly glycosylated glycoprotein hormone that mimics luteinizing hormone, binding Leydig cell receptors to stimulate testosterone production. Its 24-36 hour half-life provides sustained endocrine activation, rendering it essential for gonadal axis restoration research.
Glutathione operates via complex enzymatic and non-enzymatic redox pathways.
GHRP-6 Acetate is a first-generation synthetic hexapeptide that mimics the hunger hormone ghrelin, potently activating the GHSR-1a receptor to stimulate growth hormone release. It induces a pronounced orexigenic response, rendering it a valuable tool for appetite stimulation and GH secretagogue research.
GHRP-2 Acetate (Pralmorelin) is a second-generation synthetic hexapeptide that acts as a potent ghrelin receptor agonist, triggering reliable growth hormone release from pituitary somatotrophs. With higher GHSR-1a affinity than GHRP-6 and minimal appetite stimulation, it is ideal for evaluating GH pulsatility.
Glow is a highly advanced, tri-part combined-action peptide matrix engineered for extensive tissue remodeling.
GDF-8 Myostatin Propeptide is the recombinant N-terminal prodomain that binds and neutralizes mature myostatin with high specificity, preventing ActRIIB engagement and releasing satellite cell-mediated muscle growth. Overexpression models demonstrate up to 200% increase in skeletal muscle mass.
FOXO4-DRI is a pioneering D-Retro-Inverso senolytic peptide that disrupts the FOXO4-p53 interaction in senescent cells, releasing p53 to trigger BAX/BAK-mediated apoptosis. This selective elimination of zombie cells reduces the senescence-associated secretory phenotype for geroscience research.
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