Histone H2A-like 1 (H2AL1a) is a significant player in the intricate world of chromatin biology. This histone variant, often referred to as a "replacement histone," serves as a critical component of chromatin, the complex structure that packages DNA within the cell nucleus. H2AL1a fulfills a unique role in regulating gene expression and chromatin dynamics, distinct from its conventional histone counterparts. Unlike canonical histones, H2AL1a exhibits distinct properties and is associated with specific genomic regions, including gene promoters and enhancers, where it plays a pivotal role in orchestrating gene expression. The primary function of histone H2AL1a is to modulate chromatin structure and accessibility to DNA, thereby influencing gene expression. It achieves this by integrating various epigenetic modifications and signaling pathways within the cell. H2AL1a is known to be associated with open chromatin configurations, facilitating the binding of transcription factors and other regulatory proteins to specific gene loci. This association with active chromatin regions suggests that H2AL1a is a crucial contributor to the regulation of gene expression, allowing for dynamic responses to cellular signals and environmental cues.
The activation of histone H2AL1a involves a complex interplay of molecular mechanisms. Various chemicals and signaling pathways can influence its activation. These mechanisms include histone acetylation through inhibition of histone deacetylases (HDACs), modulation of transcription factor activities, and regulation of key cellular pathways such as the NF-κB and Wnt/β-catenin pathways. These processes ultimately lead to alterations in chromatin structure and gene expression patterns, allowing H2AL1a to fulfill its role in chromatin dynamics. In summary, histone H2A-like 1 is a vital player in the intricate choreography of chromatin regulation, contributing to the precise control of gene expression within the cell. Its activation involves a sophisticated network of epigenetic modifications and signaling pathways that collectively maintain the dynamic equilibrium of chromatin, ensuring proper gene expression in response to various cellular 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 | |
Sodium butyrate is known to activate histone H2A-like 1 by inhibiting histone deacetylase (HDAC) enzymes, leading to increased histone acetylation and transcriptional activation of target genes. | ||||||
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 is a potent HDAC inhibitor that can activate histone H2A-like 1 by promoting histone hyperacetylation, allowing for enhanced gene expression through open chromatin structures. | ||||||
Resveratrol | 501-36-0 | sc-200808 sc-200808A sc-200808B | 100 mg 500 mg 5 g | $60.00 $185.00 $365.00 | 64 | |
Resveratrol activates histone H2A-like 1 indirectly by modulating the SIRT1 pathway. It inhibits SIRT1, a deacetylase enzyme, resulting in increased histone acetylation and gene activation. | ||||||
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 activates histone H2A-like 1 through the inhibition of NF-κB signaling pathway. It reduces NF-κB activity, leading to decreased repression of target genes associated with H2A-like 1. | ||||||
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 indirectly activates histone H2A-like 1 by binding to retinoic acid receptors (RARs). RARs then act as transcription factors, facilitating gene expression and H2A-like 1 activation. | ||||||
Valproic Acid | 99-66-1 | sc-213144 | 10 g | $85.00 | 9 | |
Valproic acid is an HDAC inhibitor that activates histone H2A-like 1 by increasing histone acetylation levels, promoting open chromatin structure, and enhancing gene transcription. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $88.00 $342.00 | 284 | |
SB203580 activates histone H2A-like 1 indirectly by inhibiting p38 MAPK. Reduced p38 activity leads to increased gene expression and activation of H2A-like 1-associated pathways. | ||||||
A-769662 | 844499-71-4 | sc-203790 sc-203790A sc-203790B sc-203790C sc-203790D | 10 mg 50 mg 100 mg 500 mg 1 g | $180.00 $726.00 $1055.00 $3350.00 $5200.00 | 23 | |
A-769662 activates histone H2A-like 1 by stimulating AMP-activated protein kinase (AMPK), which regulates cellular energy homeostasis and enhances transcriptional activation of target genes. | ||||||
Dimethyl Sulfoxide (DMSO) | 67-68-5 | sc-202581 sc-202581A sc-202581B | 100 ml 500 ml 4 L | $30.00 $115.00 $900.00 | 136 | |
Dimethyl sulfoxide (DMSO) can activate histone H2A-like 1 by acting as a vehicle for other activators. It enhances the cellular uptake of other chemicals, facilitating their effects on gene expression. | ||||||
SB-216763 | 280744-09-4 | sc-200646 sc-200646A | 1 mg 5 mg | $70.00 $198.00 | 18 | |
SB216763 activates histone H2A-like 1 indirectly by inhibiting GSK-3β, leading to increased β-catenin stability and activation of Wnt/β-catenin signaling, which in turn activates target genes. | ||||||