Bromodomain (BrD) activators, also known as Brm activators, represent a specialized class of small molecules that exert their influence at the molecular level within the realm of epigenetics. Epigenetics refers to the study of heritable changes in gene expression that do not involve alterations to the DNA sequence itself but rather modifications to the chromatin structure, which encompasses DNA wrapped around histone proteins. Specifically, Brm activators target a specific class of proteins known as bromodomain-containing proteins, which are key players in the regulation of gene expression. These proteins possess bromodomains, specialized modules that recognize and bind to acetylated lysine residues on histone proteins, enabling them to act as transcriptional co-regulators.
Brm activators, as the name suggests, enhance the activity of bromodomain-containing proteins by promoting their binding to acetylated histones. This interaction, facilitated by the activator molecules, leads to a cascade of events that can modulate gene expression. By augmenting the recognition and binding of bromodomains to acetylated histones, Brm activators can potentiate or attenuate gene transcription, depending on the specific context. This fine-tuning of gene expression plays a crucial role in various cellular processes, including cell differentiation, proliferation, and response to environmental cues.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
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 | |
As a short-chain fatty acid, it acts as a histone deacetylase inhibitor, potentially leading to the upregulation of BRM expression through epigenetic changes. | ||||||
(−)-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 major component of green tea has been shown to influence various signaling pathways and epigenetic modifications, potentially affecting BRM expression. | ||||||