Date published: 2025-9-12

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JIK Activators

JIK, also known as TAOK3, is a serine/threonine protein kinase that plays a crucial role in various cellular processes. This kinase is part of the larger TAOK family, which are known to be involved in the regulation of the MAP kinase signaling pathways. JIK specifically interacts with the p38/MAPK14 and MAPK8/JNK signaling cascades, acting as an activator for the former and an inhibitor for the latter. Such dual functionality underscores the protein's intricate role in cellular homeostasis and the stress response. The expression of JIK is ubiquitous, with notable levels detected in the brain and prostate, indicating its fundamental role across diverse tissue types. The regulation of JIK's expression is a finely tuned process, as it is a pivotal component of the cell's response to environmental stresses. This kinase's activity can be regulated at multiple levels, including transcriptional, post-transcriptional, and post-translational modifications, reflecting the complex nature of cellular signaling networks.

The expression of JIK is susceptible to induction by a variety of chemical compounds, which can stimulate its activity through different molecular mechanisms. Compounds such as resveratrol and curcumin have been observed to initiate transcriptional changes that could lead to increased JIK expression. For instance, resveratrol, a polyphenol found in grapes, can activate sirtuin pathways, potentially resulting in the enhanced expression of kinases akin to JIK. Similarly, curcumin, a component of turmeric, is known to initiate a cascade of transcriptional events via the activation of transcription factors that could ultimately lead to an upsurge in JIK levels. Other molecules, like epigallocatechin gallate (EGCG) found in green tea, and sulforaphane, a sulfur-rich compound in cruciferous vegetables, have also been associated with the activation of antioxidant defense mechanisms, which might stimulate the expression of JIK. Such compounds interact with cellular signaling pathways, potentially leading to the upregulation of JIK expression as part of the cell's adaptive response to oxidative stress. These interactions highlight the intricate web of cellular signaling and the potential for various exogenous molecules to influence the expression of key regulatory proteins like JIK.

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