Date published: 2025-10-28

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ZNF302 Activators

ZNF302 can influence its activity through various biochemical pathways. Forskolin is known to activate adenylate cyclase, which catalyzes the conversion of ATP to cAMP, a secondary messenger with wide-ranging cellular effects. The increase in cAMP levels can then activate protein kinase A (PKA), which is known to phosphorylate various transcription factors. This phosphorylation can lead to changes in the conformation and function of these transcription factors, such as ZNF302, which may enhance their DNA-binding activity and increase transcriptional activity. Similarly, PMA activates protein kinase C (PKC), which phosphorylates serine and threonine residues on many substrates, including transcription factors. The activation of PKC can result in the phosphorylation of ZNF302, modifying its activity as a transcription factor.

Ionomycin raises intracellular calcium levels, which can activate calcium-dependent protein kinases that may phosphorylate ZNF302, thereby influencing its function. Epigallocatechin gallate (EGCG) and Resveratrol can modulate various signaling pathways that impact transcription factors. EGCG may enhance ZNF302's DNA-binding activity, whereas Resveratrol activates the sirtuin pathway, which can affect gene expression by modifying chromatin structure, hence potentially facilitating ZNF302's access to DNA. Spermine, through its modulation of ion channels, can create an intracellular environment that supports the activation of ZNF302. Retinoic acid alters gene expression and cellular differentiation, which may lead to a chromatin context that supports ZNF302 activation. Providing essential cofactors for ZNF302's function, Zinc sulfate supplies zinc ions, crucial for the structural integrity of zinc finger domains within ZNF302, which can directly enhance its DNA-binding capability and activation. Similarly, Dibutyryl-cAMP, a cAMP analog, activates PKA and could have a parallel effect to Forskolin, leading to the activation of ZNF302. Trichostatin A, a histone deacetylase inhibitor, can increase the accessibility of chromatin, allowing ZNF302 better access to its recognition sequences in DNA. Finally, Curcumin, by affecting numerous signaling pathways, can create conditions that promote the transcriptional activity of ZNF302.

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