Forskolin acts as a catalyst to adenylate cyclase, thereby amplifying cAMP levels, which in turn can activate proteins responsive to this messenger. PMA activates protein kinase C, an enzyme with a broad range of protein substrates, potentially impacting phosphorylation-dependent regulation mechanisms. Calcium ionophores like Ionomycin offer a route to increase intracellular calcium, a pivotal ion in numerous signaling cascades, possibly impacting calcium-binding proteins.
Rapamycin, a well-known mTOR inhibitor, prompts autophagic processes which might affect proteins that are degraded or recycled in this pathway. Inhibitors such as SB203580, LY294002, U0126, and SP600125 selectively target key kinases within MAPK, PI3K/Akt, MEK, and JNK signaling pathways, respectively, thereby altering the phosphorylation status and consequent activity of proteins intricately linked to these pathways. Epigenetic modulators wield their influence on gene expression; Trichostatin A inhibits histone deacetylases, while 5-Azacytidine targets DNA methyltransferases, each potentially leading to altered transcription and upregulation of various proteins. Resveratrol and Curcumin engage sirtuin and NF-κB pathways, which are central to cellular stress responses and inflammation, thereby modulating related protein activities.
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