Date published: 2025-10-13

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GAGE12F Activators

Chemical activators of GAGE12F can initiate a diverse array of biochemical signaling cascades resulting in its activation. Phorbol 12-myristate 13-acetate (PMA) is a potent activator of protein kinase C (PKC), and upon activation, PKC can phosphorylate a suite of proteins, including GAGE12F, which can lead to its functional activation. Forskolin, by elevating cyclic AMP (cAMP) levels, activates protein kinase A (PKA), a kinase that can phosphorylate target proteins such as GAGE12F, thereby facilitating its activation. Ionomycin, through its ability to increase intracellular calcium levels, can activate calcium-dependent kinases which, in turn, are capable of phosphorylating and activating GAGE12F. Similarly, A-23187 (Calcimycin) acts as a calcium ionophore and has a comparable effect on intracellular calcium, leading to the activation of kinases that can phosphorylate GAGE12F.

Okadaic acid and Calyculin A, both inhibitors of protein phosphatases 1 and 2A, can indirectly contribute to the activation of GAGE12F by preventing dephosphorylation, thus maintaining GAGE12F in an activated state. Sodium fluoride, another inhibitor of serine/threonine phosphatases, can also maintain the phosphorylation and consequent activation of GAGE12F. Anisomycin activates stress-activated protein kinases, which can lead to the phosphorylation of GAGE12F as part of the cellular stress response, while hydrogen peroxide activates redox-sensitive kinases that could phosphorylate and activate GAGE12F in response to oxidative stress. Epidermal Growth Factor (EGF) stimulates its receptor to initiate a phosphorylation cascade that can include kinases targeting GAGE12F for activation. 4β-Phorbol, like PMA, is a direct activator of PKC which can lead to the phosphorylation and subsequent activation of GAGE12F. Lastly, Dibutyryl-cAMP (db-cAMP) mimics cAMP action and activates PKA, which can target GAGE12F for phosphorylation and activation, thereby integrating GAGE12F into broader cellular signaling pathways.

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