Items 21 to 30 of 113 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
5-Aza-2′-Deoxycytidine | 2353-33-5 | sc-202424 sc-202424A sc-202424B | 25 mg 100 mg 250 mg | $214.00 $316.00 $418.00 | 7 | |
5-Aza-2′-Deoxycytidine is a potent inhibitor of DNA methylation, playing a pivotal role in gene regulation by altering epigenetic landscapes. It integrates into DNA, disrupting the activity of DNA methyltransferases, which leads to the reactivation of silenced genes. This compound influences chromatin structure and accessibility, promoting transcriptional activation. Its unique ability to mimic cytidine allows for specific incorporation into DNA, thereby modulating gene expression dynamics and cellular differentiation pathways. | ||||||
α-Sarcin | 86243-64-3 | sc-204427 | 1 mg | $316.00 | 6 | |
α-Sarcin is a ribonuclease that selectively cleaves RNA, impacting gene regulation by disrupting mRNA stability and translation. Its unique interaction with ribosomal RNA alters the ribosome's function, leading to inhibition of protein synthesis. This compound exhibits specificity for certain RNA sequences, influencing cellular pathways and gene expression profiles. By modulating RNA interactions, α-Sarcin plays a critical role in post-transcriptional regulation, affecting cellular responses and developmental processes. | ||||||
5-Fluoroorotic acid monohydrate | 220141-70-8 | sc-217188 | 1 g | $77.00 | ||
5-Fluoroorotic acid monohydrate is a potent inhibitor of orotate phosphoribosyltransferase, a key enzyme in the pyrimidine biosynthesis pathway. By disrupting nucleotide synthesis, it influences RNA metabolism and gene expression. Its unique structural properties allow it to mimic natural substrates, leading to competitive inhibition. This compound's ability to alter cellular nucleotide pools can significantly impact transcriptional regulation and cellular proliferation, making it a valuable tool in gene regulation studies. | ||||||
RNA Polymerase III Inhibitor Inhibitor | 577784-91-9 | sc-222257 | 10 mg | $367.00 | 1 | |
RNA Polymerase III Inhibitor selectively targets RNA polymerase III, a crucial enzyme in the transcription of small RNAs, including tRNAs and 5S rRNA. By binding to the enzyme's active site, it disrupts the transcription process, leading to decreased synthesis of these essential molecules. This inhibition alters the balance of RNA species within the cell, affecting various cellular pathways and gene expression profiles, thereby providing insights into the regulation of gene activity and RNA processing. | ||||||
GSK J1 | 1373422-53-7 | sc-391113 sc-391113A | 10 mg 50 mg | $189.00 $797.00 | ||
GSK J1 is a selective inhibitor of the transcription factor c-Myc, which plays a pivotal role in regulating gene expression and cellular proliferation. By disrupting the interaction between c-Myc and its target DNA sequences, GSK J1 modulates downstream signaling pathways, influencing cellular metabolism and growth. Its unique mechanism of action highlights the intricate balance of transcriptional regulation, offering a deeper understanding of gene control dynamics in various biological contexts. | ||||||
VAHA | 106132-78-9 | sc-364642 sc-364642A | 5 mg 25 mg | $64.00 $341.00 | 1 | |
VAHA is a potent gene regulation reagent that acts by selectively targeting and modifying histone acetylation patterns, thereby influencing chromatin structure and accessibility. This modulation enhances or represses transcriptional activity through specific interactions with transcriptional co-activators and repressors. Its unique ability to fine-tune epigenetic landscapes allows for precise control over gene expression, shedding light on the complexities of cellular differentiation and response mechanisms. | ||||||
Histone Lysine Methyltransferase Inhibitor Inhibitor | 935693-62-2 free base | sc-202651 | 5 mg | $148.00 | 4 | |
Histone Lysine Methyltransferase Inhibitor is a specialized gene regulation reagent that disrupts the methylation of lysine residues on histones, altering chromatin dynamics. By inhibiting specific methyltransferases, it influences the recruitment of chromatin remodelers and transcription factors, thereby modulating gene expression. This compound plays a crucial role in delineating the intricate balance of epigenetic modifications, impacting cellular processes such as differentiation and gene silencing. | ||||||
AMI-1, free acid | 134-47-4 | sc-300192 | 1 g | $96.00 | ||
AMI-1, free acid, serves as a potent gene regulation reagent by selectively targeting and inhibiting histone demethylases. This action leads to the accumulation of methylated histones, thereby stabilizing chromatin structure and influencing transcriptional activity. Its unique ability to modulate the epigenetic landscape allows for precise control over gene expression pathways, facilitating research into cellular mechanisms and the dynamics of gene regulation. | ||||||
NFκB Activation Inhibitor III | 380623-76-7 | sc-204818 | 5 mg | $115.00 | 3 | |
NFκB Activation Inhibitor III functions as a specialized gene regulation reagent by disrupting the NFκB signaling pathway. It binds to specific proteins involved in the pathway, preventing their activation and subsequent translocation to the nucleus. This inhibition alters the expression of target genes associated with inflammation and immune responses. Its unique mechanism of action provides insights into cellular signaling networks and the intricate balance of gene regulation. | ||||||
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
5-Azacytidine serves as a potent gene regulation reagent by incorporating into RNA and DNA, leading to the inhibition of DNA methyltransferases. This incorporation disrupts normal methylation patterns, resulting in altered gene expression. Its unique ability to modify epigenetic landscapes allows for the reactivation of silenced genes, influencing cellular differentiation and development. The compound's interaction with nucleic acids highlights its role in epigenetic regulation and gene expression dynamics. | ||||||