Date published: 2025-9-20

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V1RC16 Activators

Chemical activators of V1RC16 can have various mechanisms of action to promote the protein's activation. Zinc Chloride introduces zinc ions that can bind to V1RC16's allosteric sites, causing conformational changes that activate the protein. Similarly, Copper(II) Sulfate supplies copper ions, which may serve as cofactors for kinases that phosphorylate V1RC16, leading to its activation. Magnesium Sulfate plays a crucial role by providing magnesium ions essential for ATP binding and kinase function, leading to phosphorylation and activation of V1RC16.

Calcium Chloride contributes calcium ions that activate V1RC16 through calcium-dependent signaling pathways, inducing changes that activate the protein. Sodium Bicarbonate can alter the intracellular pH, which in turn activates V1RC16, as it responds to pH changes that affect its conformation and activity. Ammonium Chloride can cause intracellular acidification, leading to activation of V1RC16 through conformational changes. Lithium Chloride influences second messenger systems, which can lead to the activation of V1RC16 by downstream signaling events. Additionally, Cobalt(II) Chloride provides cobalt ions that can enhance kinase activity, phosphorylating and activating V1RC16. Silver Nitrate supplies silver ions that interact with V1RC16, causing alterations in the protein's structural domains and leading to its activation. Iron(III) Chloride contributes iron ions that participate in redox reactions, activating V1RC16 through oxidative modifications. Potassium Chloride affects the membrane potential, which activates V1RC16 as changes in the potential can trigger activation-associated conformational changes. Finally, Sodium Chloride influences ionic strength and electrochemical gradients, which activate V1RC16 by causing shifts in conformation necessary for its activity.

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