α-Centractin, a central element in the composition of the dynactin complex, plays a pivotal role in the cellular mechanics of vesicle and organelle transport along microtubules. As an actin-related protein, it is integral to the propulsive force that enables dynein motors to move cargo within the cell. This process is essential for a variety of cellular functions, including mitosis, where it contributes to the organization and separation of chromosomes, as well as in the transport of neurotransmitters in neuronal cells. The proper expression and function of α-centractin are thus critical for maintaining cellular homeostasis and ensuring the correct execution of intracellular trafficking.
On a molecular level, the expression of proteins like α-centractin can be influenced by a myriad of intracellular signals and environmental stimuli, leading to the modulation of their gene transcription. Certain chemical compounds have been identified that can potentially act as activators for the expression of proteins, and by extension, may play a role in the upregulation of α-centractin. These activators can engage with cellular signaling pathways, transcription factors, or epigenetic modifiers, thereby initiating a cascade of biochemical events that result in increased mRNA synthesis for the target protein. For instance, compounds that elevate intracellular cAMP levels can activate protein kinase A (PKA) and subsequently influence gene expression through transcriptional regulators like the CREB protein. Similarly, molecules that modify the epigenetic landscape, such as histone deacetylase inhibitors, can change the chromatin structure around gene promoters, thus facilitating the recruitment of transcription machinery and enhancing gene expression. Although these mechanisms offer a glimpse into the possible ways α-centractin expression could be upregulated, it's important to note that the specific effects of such compounds need to be validated through rigorous scientific investigation.
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 can upregulate cAMP levels, potentially stimulating the transcription of genes through cAMP response element-binding protein (CREB), which may include genes coding for α-centractin. | ||||||
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 can activate retinoic acid receptors, leading to the induction of gene expression related to cell differentiation and possibly upregulating α-centractin as part of a cellular differentiation program. | ||||||
(−)-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 may stimulate the activity of Nrf2, a transcription factor that can upregulate antioxidant response genes and could conceivably include genes such as α-centractin among its targets. | ||||||
Dexamethasone | 50-02-2 | sc-29059 sc-29059B sc-29059A | 100 mg 1 g 5 g | $76.00 $82.00 $367.00 | 36 | |
Dexamethasone binds to glucocorticoid receptors, which may induce the expression of anti-inflammatory response genes, potentially including those for structural proteins like α-centractin. | ||||||
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 an increase in acetylated histones and a more open chromatin state that can stimulate the expression of various genes, potentially including α-centractin. | ||||||
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
By inhibiting DNA methyltransferase, 5-Azacytidine can cause hypomethylation of DNA, which may result in the upregulation of genes that were previously silenced, possibly extending to α-centractin. | ||||||
Lithium | 7439-93-2 | sc-252954 | 50 g | $214.00 | ||
Lithium chloride can inhibit GSK-3β within the Wnt signaling pathway, leading to stabilization of β-catenin and stimulation of Wnt-target gene expression, which may include genes like α-centractin. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $62.00 $155.00 $320.00 | 233 | |
Rapamycin inhibits mTOR signaling, which can lead to the activation of autophagy and could upregulate a range of genes, potentially including those related to cytoskeletal dynamics like α-centractin. | ||||||
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's inhibition of histone deacetylase can result in increased histone acetylation, creating an environment that could stimulate the transcription of various genes including potentially α-centractin. | ||||||
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 (PKC), which can lead to the activation of transcription factors and subsequent upregulation of a suite of genes, possibly encompassing α-centractin. |