Date published: 2025-9-25

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Nup62-il4i1 Activators

Chemical activators of Nup62-il4i1 can engage with the protein through various biochemical pathways to enhance its functional activity. Zinc Chloride and Magnesium Chloride can act as cofactors, essential for the structural integrity and enzymatic functions of Nup62-il4i1, ensuring it maintains the correct conformation for activation and can be efficiently phosphorylated by kinases. Sodium Fluoride can act as an allosteric effector, enhancing the phosphorylation state of Nup62-il4i1, a modification that is often critical for the activation of proteins. In a similar vein, Forskolin raises the levels of intracellular cAMP, which in turn activates protein kinase A (PKA). PKA can directly phosphorylate Nup62-il4i1, leading to its activation. Phorbol 12-myristate 13-acetate (PMA) activates protein kinase C (PKC), another kinase that can phosphorylate and thereby activate Nup62-il4i1.

Ionomycin works by increasing intracellular calcium levels, which activates calcium-dependent kinases capable of phosphorylating Nup62-il4i1. Hydrogen Peroxide serves as a signaling molecule that can activate kinases, which are involved in the phosphorylation and subsequent activation of Nup62-il4i1. Okadaic Acid prolongs the phosphorylation state of Nup62-il4i1 by inhibiting the action of protein phosphatases that would otherwise dephosphorylate and deactivate the protein. 4-Phenylbutyric Acid ensures proper folding and intracellular localization of Nup62-il4i1, which is a prerequisite for its activation. Chloroquine also influences the trafficking and folding of Nup62-il4i1, thus promoting its activation. Nicotine, by acting on nicotinic acetylcholine receptors, leads to an influx of calcium, which activates kinases that can phosphorylate Nup62-il4i1. Finally, Lithium Chloride can influence the GSK-3β signaling pathways, affecting proteins that are associated with Nup62-il4i1 and may lead to its activation through phosphorylation events. Together, these chemicals engage with and activate Nup62-il4i1 through a synergy of stabilization, trafficking, and post-translational modifications such as phosphorylation.

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