PIWIL4 Activators encompass a range of chemical compounds that indirectly enhance the functional activity of PIWIL4, primarily through the modulation of biochemical and cellular pathways crucial for PIWIL4's role in piRNA-guided gene silencing and genomic integrity. Zinc Sulfate and Manganese (II) Chloride directly support PIWIL4's structural and enzymatic requirements, stabilizing the PIWI domain and acting as cofactors for associated enzymes, respectively. This stabilization is vital for PIWIL4's interaction with piRNAs and subsequent RNA silencing. Similarly, Magnesium Sulfate and Copper (II) Sulfate contribute to PIWIL4's RNA-binding activity and enzymatic function, which are central to its role in piRNA-mediated gene regulation. Furthermore, metabolic precursors and cofactors like Nicotinamide Mononucleotide (NMN), Beta-Nicotinamide Adenine Dinucleotide (NAD+), and Acetyl-L-Carnitine indirectly support PIWIL4 activity. NMN and NAD+ enhance PIWIL4's involvement in transcriptional gene silencing by modulating cellular metabolic states, while Acetyl-L-Carnitine aids mitochondrial function, essential for PIWIL4's role in germ cell development.
In addition, antioxidants such as Sodium Selenite, Alpha-Lipoic Acid, and Glutathione Reduced play a crucial role in maintaining the functional integrity of PIWIL4. These compounds contribute to the cellular antioxidant defense, protecting PIWIL4 against oxidative stress and ensuring its effective participation in piRNA pathways. Vitamins and nutrients like Folic Acid and Vitamin B12 further augment PIWIL4's function. Folic Acid facilitates methylation reactions, which are integral to PIWIL4's epigenetic regulation activities, while Vitamin B12 is essential for DNA synthesis and repair, thereby supporting PIWIL4's role in maintaining genomic stability. Collectively, these PIWIL4 Activators, through their targeted influence on cellular and molecular mechanisms, facilitate the enhancement of PIWIL4-mediated functions in gene regulation, genome defense, and germ cell development, reflecting the intricate interplay of nutritional and biochemical factors in the regulation of piRNA pathways.
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