MRP-L28, or Mitochondrial Ribosomal Protein L28, is a fundamental component of the mitochondrial ribosome, which is pivotal in the synthesis of proteins that are encoded by the mitochondrial genome. These proteins are essential for the mitochondrial respiratory chain, a crucial aspect of cellular energy production in the form of adenosine triphosphate (ATP). MRP-L28 not only contributes to the structural integrity of the ribosomal complex but also plays a significant role in the translation process of mitochondrial DNA transcripts. The regulation of MRP-L28 expression is a sophisticated affair, intertwined with the broader network of cellular metabolism, stress responses, and mitochondrial biogenesis. Given its central role, the expression of MRP-L28 is a finely tuned process, responsive to the intricate demands placed upon the cell's energy production systems.
The expression of MRP-L28 can be potentially upregulated by a variety of chemical activators, which exert their effects through diverse biological pathways that converge on mitochondrial functionality and biogenesis. Compounds such as resveratrol and metformin can initiate signaling cascades that culminate in the enhancement of mitochondrial number and efficiency, which may necessitate the increased production of MRP-L28 to meet the demands of the expanded ribosomal machinery. Other molecules, such as sulforaphane and curcumin, are known to activate cellular defense mechanisms against oxidative stress, which could lead to an upsurge in mitochondrial protective measures, including the synthesis of MRP-L28. Additionally, molecules like Bezafibrate and PPAR agonists, such as Pioglitazone, engage in the modulation of lipid metabolism and energy homeostasis, processes that are inherently linked to mitochondrial function and could thereby upregulate the expression of mitochondrial ribosomal proteins such as MRP-L28. Precursors to NAD+ like Nicotinamide riboside also play a role in cellular metabolism and longevity, and by enhancing mitochondrial performance, might indirectly promote the production of proteins essential for mitochondrial resilience and adaptability. It is through these multifaceted biological interactions that such compounds could potentially increase the expression of MRP-L28, reflecting the dynamic nature of cellular adaptogenic responses to environmental and metabolic cues.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Resveratrol | 501-36-0 | sc-200808 sc-200808A sc-200808B | 100 mg 500 mg 5 g | $60.00 $185.00 $365.00 | 64 | |
Resveratrol may upregulate MRP-L28 by enhancing the number of mitochondria within cells, as it has been shown to stimulate mitochondrial biogenesis through the activation of the SIRT1/PGC-1α pathway. | ||||||
Metformin | 657-24-9 | sc-507370 | 10 mg | $77.00 | 2 | |
Metformin could stimulate an increase in MRP-L28 expression through the activation of AMP-activated protein kinase (AMPK), which promotes mitochondrial biogenesis and, as a result, may require an upsurge in mitochondrial ribosomal components. | ||||||
D,L-Sulforaphane | 4478-93-7 | sc-207495A sc-207495B sc-207495C sc-207495 sc-207495E sc-207495D | 5 mg 10 mg 25 mg 1 g 10 g 250 mg | $150.00 $286.00 $479.00 $1299.00 $8299.00 $915.00 | 22 | |
DL-Sulforaphane has been shown to activate the Nrf2 pathway, which is a key regulator in the cellular defense against oxidative stress. This activation could lead to an upsurge in the production of mitochondrial components, including MRP-L28. | ||||||
Curcumin | 458-37-7 | sc-200509 sc-200509A sc-200509B sc-200509C sc-200509D sc-200509F sc-200509E | 1 g 5 g 25 g 100 g 250 g 1 kg 2.5 kg | $36.00 $68.00 $107.00 $214.00 $234.00 $862.00 $1968.00 | 47 | |
Curcumin may stimulate the expression of MRP-L28 by promoting the assembly and maintenance of mitochondria. Its antioxidative properties could necessitate an increase in mitochondrial protein synthesis to maintain mitochondrial integrity. | ||||||
AICAR | 2627-69-2 | sc-200659 sc-200659A sc-200659B | 50 mg 250 mg 1 g | $60.00 $270.00 $350.00 | 48 | |
As an AMPK activator, AICAR may stimulate the synthesis of mitochondrial proteins, including MRP-L28, by promoting mitochondrial biogenesis. This could lead to an increased demand for mitochondrial ribosomal proteins. | ||||||
Retinoic Acid, all trans | 302-79-4 | sc-200898 sc-200898A sc-200898B sc-200898C | 500 mg 5 g 10 g 100 g | $65.00 $319.00 $575.00 $998.00 | 28 | |
Retinoic acid could induce MRP-L28 expression through its role in cellular differentiation and growth. By influencing the differentiation of cells, it may increase the need for mitochondrial proteins, including those involved in protein synthesis. | ||||||
Pioglitazone | 111025-46-8 | sc-202289 sc-202289A | 1 mg 5 mg | $54.00 $123.00 | 13 | |
Pioglitazone, a PPAR agonist, may upregulate MRP-L28 expression by stimulating mitochondrial biogenesis. This could increase the requirement for mitochondrial ribosomal proteins to support the enhanced synthesis of mitochondrial-encoded proteins. | ||||||
Nicotinamide riboside | 1341-23-7 | sc-507345 | 10 mg | $411.00 | ||
Nicotinamide riboside, as an NAD+ precursor, may induce the expression of MRP-L28 by improving mitochondrial function and biogenesis. An increase in NAD+ levels is associated with enhanced production of mitochondrial components. | ||||||
Bezafibrate | 41859-67-0 | sc-204650B sc-204650 sc-204650A sc-204650C | 500 mg 1 g 5 g 10 g | $30.00 $45.00 $120.00 $200.00 | 5 | |
Bezafibrate may stimulate the biosynthesis of MRP-L28 through its action as a PPAR agonist. By promoting the biogenesis of mitochondria, it may lead to a rise in the demand for the proteins that constitute the mitochondrial ribosome. | ||||||
(−)-Epigallocatechin Gallate | 989-51-5 | sc-200802 sc-200802A sc-200802B sc-200802C sc-200802D sc-200802E | 10 mg 50 mg 100 mg 500 mg 1 g 10 g | $42.00 $72.00 $124.00 $238.00 $520.00 $1234.00 | 11 | |
Epigallocatechin Gallate has the potential to stimulate MRP-L28 production due to its effects on mitochondrial function and biogenesis. The compound's antioxidant properties may also necessitate an increase in mitochondrial protein synthesis for cellular defense. | ||||||