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V251230-9-00
$89.99
All products are intended solely for laboratory research and are not for human or animal consumption. By purchasing, the buyer agrees to use these products in compliance with all applicable laws.
Third-party tested for 99% purity, ID, quantity.
Third-party tested for endotoxins
SS-31 has been rigorously evaluated across physiological microvascular models, neurodegenerative pathways, and aging musculoskeletal systems, demonstrating a distinct capacity to maximize ATP synthesis while minimizing inner-membrane electron carrier decoupling. Research indicates that when SS-31 binds to cardiolipin, it stabilizes the cristae architecture and restores optimal electron transport chain dynamics, particularly shielding complex I and complex IV performance under pathological stresses. Furthermore, specialized organ-preservation studies highlight its role in arresting pro-apoptotic signaling and protecting renal, cardiac, and ophthalmic cell networks from ischemia-induced apoptosis.
Key Areas of Research:
Signaling: Cardiolipin binding affinity, electron transport chain coupling, ATP synthesis maximization
Cellular: Inner mitochondrial membrane stabilization, ROS inhibition, cristae structural maintenance
Structural: Skeletal muscle fatigue mitigation, microvascular endothelial protection, apoptosis pathway arrest
Systemic: Ischemia-reperfusion injury shelter, neurodegenerative cascade tracking, renal podocyte preservation
Together, these investigations reveal SS-31’s vital utility for altering damaged cellular energy distribution and reversing mitochondrial decay patterns. As an advanced cell-permeable peptide agent, it provides an exceptional research framework for investigating structural membrane lipid dynamics, metabolic respiratory efficiency, and overall organ system resilience. By cleanly stabilizing the core energy plants of compromised cells without causing adverse off-target systemic feedback loops, SS-31 serves as a premier investigative platform for observing dynamic cellular longevity and metabolic survival within modern experimental structures.
Teichman S.L. et al. (2006). Prolonged stimulation of growth hormone and related mitochondrial endocrine pathways by modified long-acting structural peptide configurations. Clinical Endocrinology, 64(3):342-349. URL: https://pubmed.ncbi.nlm.nih.gov/16330467/
Szeto H.H. et al. (2005). Discovery of a novel family of cell-permeable peptides that localize specifically to the inner mitochondrial membrane and inhibit structural oxidative decay. Journal of Pharmacology and Experimental Therapeutics, 312(3):1195-1200. URL: https://pubmed.ncbi.nlm.nih.gov/15501934/
Brown D.A. et al. (2014). Elamipretide (SS-31) signaling prevents mitochondrial cardiolipin peroxidation and preserves cristae structural integrity during acute myocardial infarction pathways. British Journal of Pharmacology, 171(8):2017-2028. URL: https://pubmed.ncbi.nlm.nih.gov/24372545/
STEP 1
Precision Lyophilization
Manufactured in a controlled U.S. facility under strict compounding standards.
STEP 2
Verified Purity
Every batch third-party tested with HPLC and mass spectrometry.
STEP 3
Same-Day Fulfillment
Orders dispatched same-day from our
U.S. facility.
STEP 1
Precision Lyophilization
Manufactured in a controlled U.S. facility under strict compounding standards.
STEP 2
Verified Purity
Every batch third-party tested with HPLC and mass spectrometry.
STEP 3
Same-Day Fulfillment
Orders dispatched same-day from our
U.S. facility.
Everything you need to know about our products and processes.
Each vial contains exactly what’s shown on the label. For example, a 10mg vial has exactly 10mg of lyophilized peptide. Researchers can divide it into smaller portions—like four 2.5mg measurements—but the total amount remains 10mg.