Yan SF, Fujita T, Lu J, Okada K, Shan Zou Y, Mackman N, et al
Use with caution in patients with Lebers disease (hereditary optic nerve atrophy)
doi:10.1111/j.1572-0241.2006.00650.x Butt I, Kasmin F
Purity & Documentation Data Sheet (276 KB) SDS (393 KB) English - EN (393 KB) Franais - FR (393 KB) Deutsch - DE (393 KB) Norwegian - NO (393 KB) Espaol - ES (393 KB) Swedish - SV (393 KB) Italian - IT (393 KB) Korean - KR (393 KB) Portuguese - PT (393 KB) Handling Instructions (2659 KB) References [1]
Metabolic imbalance associated with methylation dysregulation and oxidative damage in children with autism
Unlike native IGF-1, which is rapidly bound and regulated by IGFBPs in circulation, IGF-1 LR3 was engineered to remain active longer, making it a useful tool for researchers studying sustained IGF-1 receptor signaling rather than the brief signaling windows native IGF-1 typically produces