AP-4μ, known scientifically as AP4M1, represents a crucial component of the adaptor protein complex-4 (AP-4) which is instrumental in the sorting and trafficking of proteins within cellular compartments, particularly between the trans-Golgi network and endosomes. The AP-4 complex plays a significant role in the proper functioning of neurons and is implicated in the maintenance of brain health. AP4M1 gene mutations have been linked to various neurological manifestations, highlighting the importance of this protein in neural development and signaling. The expression of AP-4μ, like many other proteins, is subject to regulation at the genetic level, implying that specific factors can induce or suppress its production within the cell. Understanding these regulatory mechanisms is critical for unraveling the complex biology of intracellular transport and its contribution to cellular homeostasis.
Research into the regulation of protein expression has identified a myriad of chemical compounds that can act as activators, potentially stimulating the production of proteins such as AP-4μ. These activators can exert their effects through diverse biological pathways, such as altering intracellular signaling cascades, modifying the epigenetic landscape, or affecting the activity of transcription factors that bind to DNA and initiate gene expression. For instance, compounds that increase the levels of intracellular cAMP can activate transcription factors through protein kinase A, leading to enhanced gene expression. Histone deacetylase inhibitors, on the other hand, can promote a more open chromatin structure, making it easier for transcription machinery to access genes and initiate their expression. Moreover, some activators work through the modulation of cellular stress pathways or nutrient-sensing mechanisms, which can result in the upregulation of genes that are involved in cellular adaptation and survival processes. While the direct activators of AP-4μ expression are still being studied, it is evident that the cellular environment and its multitude of signaling molecules play a significant role in the regulation of this protein and its associated functions within the cell.
SEE ALSO...
Items 1 to 10 of 12 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Forskolin | 66575-29-9 | sc-3562 sc-3562A sc-3562B sc-3562C sc-3562D | 5 mg 50 mg 1 g 2 g 5 g | $76.00 $150.00 $725.00 $1385.00 $2050.00 | 73 | |
Forskolin catalyzes the conversion of ATP to cAMP, escalating intracellular cAMP levels, which may stimulate the cAMP-dependent pathway leading to an increase in transcriptional activity that could upregulate AP-4μ expression. | ||||||
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 serves as a ligand for nuclear receptors that can bind to DNA response elements, thereby initiating transcription and potentially upregulating gene expression. AP-4μ expression could be increased as part of a coordinated response in cellular differentiation. | ||||||
(−)-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 | |
This catechin can activate antioxidant response elements within the promoter regions of genes, potentially stimulating the expression of genes associated with endosomal trafficking, including AP-4μ, as part of the cellular defense mechanism against oxidative stress. | ||||||
Trichostatin A | 58880-19-6 | sc-3511 sc-3511A sc-3511B sc-3511C sc-3511D | 1 mg 5 mg 10 mg 25 mg 50 mg | $149.00 $470.00 $620.00 $1199.00 $2090.00 | 33 | |
Trichostatin A inhibits histone deacetylases, leading to hyperacetylation of histones, thereby unwinding DNA and promoting transcriptional activation. This action could stimulate the transcription of genes including AP-4μ, as part of the chromatin remodeling response. | ||||||
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
5-Azacytidine induces DNA demethylation, which can lead to the reactivation of silenced genes. By demethylating promoter regions, it may enhance the transcription of AP-4μ. | ||||||
Lithium | 7439-93-2 | sc-252954 | 50 g | $214.00 | ||
Lithium chloride activates the Wnt signaling pathway, leading to increased transcriptional activity of Wnt target genes. This upsurge in gene activity may encompass genes like AP-4μ, which is implicated in intracellular protein sorting. | ||||||
Sodium Butyrate | 156-54-7 | sc-202341 sc-202341B sc-202341A sc-202341C | 250 mg 5 g 25 g 500 g | $30.00 $46.00 $82.00 $218.00 | 19 | |
Sodium butyrate, by inhibiting histone deacetylase, can lead to the hyperacetylation of histone proteins, thereby promoting an open chromatin state conducive to gene transcription. This may enhance the expression of AP-4μ by making its promoter region more accessible to transcription factors. | ||||||
PMA | 16561-29-8 | sc-3576 sc-3576A sc-3576B sc-3576C sc-3576D | 1 mg 5 mg 10 mg 25 mg 100 mg | $40.00 $129.00 $210.00 $490.00 $929.00 | 119 | |
PMA activates protein kinase C, which can phosphorylate transcription factors, thereby triggering the transcription of downstream genes. This activation cascade could lead to the upregulation of AP-4μ if its expression is under the control of such transcription factors. | ||||||
Isoproterenol Hydrochloride | 51-30-9 | sc-202188 sc-202188A | 100 mg 500 mg | $27.00 $37.00 | 5 | |
Isoproterenol binds to beta-adrenergic receptors and enhances the generation of cAMP, which can activate protein kinase A (PKA). PKA may phosphorylate transcription factors that stimulate the expression of genes like AP-4μ, involved in vesicular trafficking pathways. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $62.00 $155.00 $320.00 | 233 | |
Rapamycin is an mTOR inhibitor that can arrest cell cycle progression and protein synthesis. This inhibition may lead to a compensatory upregulation of other pathways, including those involved in vesicle formation and trafficking, potentially eliciting an increase in AP-4μ expression. | ||||||