Items 61 to 70 of 113 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
B2 | 115687-05-3 | sc-202486 sc-202486A sc-202486B | 500 µg 5 mg 25 mg | $80.00 $160.00 $700.00 | 12 | |
B2 acts as a gene regulation reagent by selectively interacting with transcription factors, enhancing or inhibiting their binding to DNA. This modulation influences chromatin remodeling and alters the recruitment of co-regulators, thereby affecting gene expression dynamics. Its unique ability to stabilize specific protein-DNA complexes allows for precise control over cellular signaling pathways, impacting processes such as cell growth and differentiation. The compound's kinetic properties facilitate rapid responses in gene regulation. | ||||||
Rosiglitazone | 122320-73-4 | sc-202795 sc-202795A sc-202795C sc-202795D sc-202795B | 25 mg 100 mg 500 mg 1 g 5 g | $118.00 $320.00 $622.00 $928.00 $1234.00 | 38 | |
Rosiglitazone functions as a gene regulation reagent by modulating the activity of peroxisome proliferator-activated receptors (PPARs), which are critical in lipid metabolism and insulin sensitivity. Its unique binding affinity alters the conformation of these receptors, influencing their interaction with co-activators and repressors. This selective modulation leads to changes in gene transcription rates, impacting metabolic pathways and cellular homeostasis. The compound's interaction dynamics enable nuanced control over gene expression profiles. | ||||||
Strontium Ranelate | 135459-87-9 | sc-208403 | 10 mg | $320.00 | ||
Strontium Ranelate acts as a gene regulation reagent by influencing signaling pathways associated with bone metabolism. It interacts with specific receptors, promoting the differentiation of osteoblasts while inhibiting osteoclast activity. This dual action alters gene expression related to bone formation and resorption. The compound's unique ability to modulate these pathways enhances cellular communication, leading to a balanced regulation of genes involved in skeletal integrity and homeostasis. | ||||||
N-(β-ketocaproyl)-L-Homoserine lactone | 143537-62-6 | sc-205396 sc-205396A | 5 mg 25 mg | $52.00 $164.00 | 2 | |
N-(β-ketocaproyl)-L-Homoserine lactone serves as a gene regulation reagent by engaging in quorum sensing mechanisms, facilitating intercellular communication among bacterial populations. Its unique structure allows it to bind to specific transcriptional regulators, influencing gene expression related to biofilm formation and virulence. The compound's ability to modulate signaling cascades enhances the coordination of cellular responses, ultimately affecting metabolic pathways and community behavior in microbial systems. | ||||||
N-octanoyl-L-Homoserine lactone | 147852-84-4 | sc-222011 sc-222011A sc-222011B sc-222011C | 5 mg 10 mg 25 mg 50 mg | $75.00 $100.00 $220.00 $380.00 | 1 | |
N-octanoyl-L-Homoserine lactone functions as a gene regulation reagent by participating in quorum sensing, where it acts as a signaling molecule that influences gene expression in response to cell density. Its distinctive acyl chain enhances lipid solubility, promoting membrane permeability and facilitating rapid cellular uptake. This compound selectively interacts with LuxR-type receptors, triggering transcriptional activation of genes involved in diverse physiological processes, including motility and bioluminescence. | ||||||
Geninthiocin | 158792-27-9 | sc-202167 | 500 µg | $359.00 | 1 | |
Geninthiocin serves as a gene regulation reagent by modulating transcriptional activity through specific interactions with DNA-binding proteins. Its unique structure allows for selective binding to regulatory elements, influencing gene expression patterns. The compound exhibits distinct reaction kinetics, facilitating rapid activation or repression of target genes. Additionally, its ability to form stable complexes with transcription factors enhances its efficacy in altering cellular responses to environmental stimuli. | ||||||
Levofloxacin hydrochloride | 177325-13-2 | sc-202693 sc-202693A | 1 g 5 g | $57.00 $103.00 | 1 | |
Levofloxacin hydrochloride functions as a gene regulation reagent by interacting with bacterial topoisomerases, crucial enzymes in DNA replication and transcription. Its unique molecular structure enables it to stabilize the enzyme-DNA complex, thereby influencing the supercoiling of DNA. This modulation affects gene expression by altering the accessibility of DNA to transcription machinery. The compound's affinity for specific nucleic acid structures enhances its role in regulating genetic pathways, impacting cellular processes. | ||||||
GW 1929 | 196808-24-9 | sc-202640 | 1 mg | $89.00 | ||
GW 1929 serves as a gene regulation reagent by selectively modulating the activity of transcription factors involved in gene expression. Its unique ability to bind to specific DNA motifs allows it to influence chromatin remodeling and transcriptional activation. This compound exhibits distinct kinetics in its interactions, promoting or inhibiting the recruitment of co-regulators, thereby fine-tuning the expression of target genes. Its specificity in molecular interactions underscores its role in cellular signaling pathways. | ||||||
AG-041R | 159883-95-1 | sc-205202 sc-205202A | 1 mg 5 mg | $73.00 $332.00 | ||
AG-041R functions as a gene regulation reagent by targeting specific epigenetic modifications, influencing histone acetylation and methylation patterns. Its unique binding affinity to regulatory elements facilitates the recruitment of chromatin remodeling complexes, thereby altering gene accessibility. The compound exhibits distinct reaction kinetics, enabling it to modulate the dynamics of transcriptional machinery, ultimately impacting gene expression profiles and cellular responses. | ||||||
N-butyryl-L-Homocysteine thiolactone | 202284-85-3 | sc-221995 sc-221995A | 5 mg 10 mg | $39.00 $101.00 | ||
N-butyryl-L-Homocysteine thiolactone serves as a gene regulation reagent by acting as a potent acylating agent, selectively modifying thiol groups in proteins. This modification can influence protein-protein interactions and alter the stability of transcription factors. Its unique reactivity allows for the formation of thioester bonds, which can impact cellular signaling pathways and transcriptional activation, thereby shaping gene expression dynamics in response to environmental cues. | ||||||