C11orf10/1810006K21Rik Activators encompass a diverse array of chemical compounds that serve to indirectly enhance the activity of C11orf10/1810006K21Rik through distinct signaling mechanisms. This enhancement is initiated by molecules such as Forskolin and Isoproterenol, which increase intracellular cAMP levels, subsequently activating PKA that can phosphorylate C11orf10/1810006K21Rik, thereby augmenting its activity. Similarly, the cAMP analog 8-Bromo-cAMP bypasses upstream adenylyl cyclase activation to directly activate PKA, leading to enhanced C11orf10/1810006K21Rik function. On another front, PMA activates PKC, which sets off a phosphorylation cascade likely to impinge upon C11orf10/1810006K21Rik, modifying its interactions and enhancing its activity, while Ionomycin elevates intracellular calcium, activating calcium-dependent kinases that may directly or indirectly phosphorylate and activate C11orf10/1810006K21Rik.
Continuing the theme of indirect activation, Genistein and EGCG, by inhibiting tyrosine and other kinases, respectively, may reduce inhibitory phosphorylation or competition, allowing for enhanced activation of C11orf10/1810006K21Rik by facilitating kinase access.
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