Items 81 to 90 of 113 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
2-Heptyl-3-hydroxyl-4-quinolone | 108985-27-9 | sc-396649 | 25 mg | $192.00 | ||
2-Heptyl-3-hydroxyl-4-quinolone functions as a gene regulation reagent by engaging in specific molecular interactions with transcription factors and regulatory proteins. Its unique quinolone structure allows for π-π stacking and hydrogen bonding, facilitating the stabilization of protein-DNA complexes. This compound can influence signaling pathways by modulating the activity of enzymes involved in gene expression, thereby impacting cellular responses. Its lipophilic nature enhances membrane permeability, promoting efficient cellular uptake and interaction with intracellular targets. | ||||||
DIF-1 | 111050-72-7 | sc-221541 sc-221541A | 100 µg 500 µg | $64.00 $255.00 | ||
DIF-1 acts as a gene regulation reagent by selectively binding to specific transcriptional co-regulators, influencing gene expression dynamics. Its unique structural features enable it to disrupt protein-protein interactions, thereby altering the assembly of transcriptional complexes. Additionally, DIF-1 exhibits a propensity for forming stable complexes with chromatin, which can modulate epigenetic modifications. This compound's hydrophobic characteristics facilitate its diffusion across cellular membranes, enhancing its bioavailability for intracellular interactions. | ||||||
tert-butyl 2-aminophenylcarbamate | 146651-75-4 | sc-356014 sc-356014A | 250 mg 1 g | $188.00 $380.00 | ||
Tert-butyl 2-aminophenylcarbamate functions as a gene regulation reagent by modulating the activity of transcription factors through competitive inhibition. Its unique amine and carbamate groups enable specific hydrogen bonding with target proteins, influencing their conformational states. This compound can also alter the recruitment of chromatin remodeling complexes, impacting gene accessibility. Its lipophilic nature promotes effective cellular uptake, allowing for significant intracellular regulatory effects. | ||||||
LED209 | 245342-14-7 | sc-205368 sc-205368A | 1 mg 5 mg | $18.00 $75.00 | ||
LED209 serves as a gene regulation reagent by selectively interacting with RNA polymerase, enhancing transcriptional activity. Its unique structure facilitates the formation of stable complexes with regulatory proteins, promoting specific gene expression profiles. The compound's ability to influence post-translational modifications of histones further modulates chromatin dynamics, thereby affecting gene accessibility. Additionally, its hydrophobic characteristics support membrane permeability, ensuring efficient cellular delivery and action. | ||||||
Fmoc-L-Lys(Me2)-OH*HCl | 252049-10-8 | sc-294919 | 250 mg | $300.00 | ||
Fmoc-L-Lys(Me2)-OH*HCl functions as a gene regulation reagent by acting as a versatile building block in peptide synthesis, enabling the incorporation of lysine residues into peptides that can modulate gene expression. Its unique Fmoc protecting group allows for selective deprotection under mild conditions, facilitating precise control over peptide assembly. The dimethylated lysine side chain enhances interactions with epigenetic modifiers, influencing chromatin structure and gene accessibility. | ||||||
CASIN | 425399-05-9 | sc-397016 | 10 mg | $460.00 | 1 | |
CASIN serves as a potent gene regulation reagent by selectively inhibiting histone deacetylases, thereby promoting an open chromatin state. Its unique structure allows for specific binding to the active site of these enzymes, altering their kinetics and enhancing acetylation levels on histones. This modulation of histone acetylation can lead to significant changes in gene expression patterns, making CASIN a valuable tool for studying epigenetic regulation. | ||||||
N-3-oxo-hexadec-11Z-enoyl-L-Homoserine lactone | 479050-91-4 | sc-221977 sc-221977A | 1 mg 5 mg | $48.00 $159.00 | ||
N-3-oxo-hexadec-11Z-enoyl-L-Homoserine lactone functions as a gene regulation reagent by engaging in quorum sensing mechanisms, facilitating intercellular communication in bacterial populations. Its unique acyl homoserine lactone structure enables it to bind to specific receptors, triggering signal transduction pathways that influence gene expression. This compound's ability to modulate transcriptional responses highlights its role in regulating diverse biological processes at the genetic level. | ||||||
N-3-oxo-tetradec-7Z-enoyl-L-Homoserine lactone | 482598-46-9 | sc-205401 sc-205401A | 1 mg 5 mg | $29.00 $129.00 | ||
N-3-oxo-tetradec-7Z-enoyl-L-Homoserine lactone acts as a gene regulation reagent by participating in bacterial quorum sensing, where it serves as a signaling molecule. Its distinctive acyl chain length and unsaturation allow for specific interactions with LuxR-type receptors, leading to the activation of target genes. This compound's precise structural features influence its binding affinity and kinetics, ultimately shaping the dynamics of gene expression and cellular behavior in microbial communities. | ||||||
UNC 0224 | 1197196-48-7 | sc-362816 sc-362816A | 10 mg 50 mg | $194.00 $816.00 | ||
UNC 0224 serves as a specialized gene regulation reagent by modulating the activity of specific transcription factors. Its unique molecular design enables it to interact with regulatory elements in DNA, influencing gene expression patterns. By stabilizing or destabilizing protein-DNA complexes, UNC 0224 can alter transcriptional dynamics. Additionally, its favorable solubility properties enhance its accessibility to cellular components, promoting effective engagement with target pathways and influencing gene regulatory networks. | ||||||
Staurosporine Solution in Ethyl Acetate | 62996-74-1 | sc-360258 | 100 µg | $92.00 | 4 | |
Staurosporine Solution in Ethyl Acetate functions as a potent gene regulation reagent by inhibiting protein kinases, which play critical roles in various signaling pathways. Its unique structure allows for selective binding to ATP-binding sites, disrupting phosphorylation processes. This interference alters downstream gene expression, affecting cellular responses. The compound's solubility in ethyl acetate enhances its bioavailability, facilitating its interaction with target proteins and influencing cellular signaling cascades. | ||||||