Items 31 to 40 of 113 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
13-cis-Retinoic acid | 4759-48-2 | sc-205568 sc-205568A | 100 mg 250 mg | $74.00 $118.00 | 8 | |
13-cis-Retinoic acid functions as a significant gene regulation reagent by modulating the activity of nuclear receptors, particularly retinoic acid receptors (RARs). This compound influences transcriptional regulation through its binding affinity, promoting the expression of genes involved in cellular differentiation and growth. Its unique ability to alter chromatin structure enhances accessibility for transcription factors, thereby impacting gene expression profiles and cellular responses. | ||||||
Bisbenzimide H 33258 Fluorochrome, Trihydrochloride | 23491-45-4 | sc-202503 sc-202503A sc-202503B | 100 mg 250 mg 1 g | $130.00 $260.00 $515.00 | 5 | |
Bisbenzimide H 33258 Fluorochrome, Trihydrochloride is a potent gene regulation reagent known for its high affinity for DNA, particularly binding to the minor groove. This interaction stabilizes the DNA structure and influences transcriptional activity by altering the accessibility of regulatory elements. Its fluorescent properties enable real-time monitoring of nucleic acid dynamics, providing insights into gene expression patterns and cellular processes. The compound's specificity for AT-rich regions further enhances its utility in studying gene regulation mechanisms. | ||||||
3-Deazaneplanocin, HCl salt | 120964-45-6 | sc-351856 sc-351856A sc-351856B | 1 mg 5 mg 10 mg | $251.00 $600.00 $918.00 | 2 | |
3-Deazaneplanocin, HCl salt is a unique gene regulation reagent that acts as a potent inhibitor of histone methylation. By targeting specific methyltransferases, it disrupts the epigenetic landscape, leading to altered gene expression profiles. Its ability to modulate chromatin structure enhances the accessibility of transcription factors, thereby influencing transcriptional activation. This compound's selective interaction with key regulatory proteins makes it a valuable tool for dissecting complex gene regulatory networks. | ||||||
Dodecanoyl-L-homoserine lactone | 137173-46-7 | sc-391777 | 5 mg | $48.00 | ||
Dodecanoyl-L-homoserine lactone is a notable gene regulation reagent that functions as a signaling molecule in quorum sensing. It facilitates intercellular communication by binding to specific receptors, triggering cascades that modulate gene expression in response to cell density. This compound's unique lactone structure allows for rapid hydrolysis, influencing reaction kinetics and stability. Its role in orchestrating collective behaviors in microbial populations highlights its significance in gene regulatory mechanisms. | ||||||
N-hexanoyl-L-Homoserine lactone | 147852-83-3 | sc-205405 sc-205405A sc-205405B sc-205405C | 5 mg 10 mg 25 mg 50 mg | $57.00 $84.00 $172.00 $325.00 | 4 | |
N-hexanoyl-L-homoserine lactone serves as a pivotal gene regulation reagent, acting as a key player in quorum sensing. Its unique acyl homoserine lactone structure enables it to interact with LuxR-type receptors, initiating complex signaling pathways that regulate gene expression based on population density. The compound's hydrophobic nature enhances membrane permeability, facilitating swift cellular uptake and subsequent biological responses, thereby influencing microbial behavior and community dynamics. | ||||||
Thyroid Hormone Receptor Antagonist, 1-850 | 251310-57-3 | sc-222357A sc-222357B sc-222357 | 1 mg 10 mg 5 mg | $75.00 $129.00 $94.00 | 2 | |
Thyroid Hormone Receptor Antagonist, 1-850 functions as a significant gene regulation reagent by selectively binding to thyroid hormone receptors, inhibiting their activity. This compound disrupts the normal hormone-receptor interactions, altering downstream signaling pathways involved in metabolic regulation. Its unique structural features allow for specific molecular interactions that modulate gene expression, impacting cellular processes and influencing developmental pathways in various biological systems. | ||||||
N-nonanoyl-L-Homoserine lactone | 177158-21-3 | sc-224145 sc-224145A | 5 mg 10 mg | $40.00 $75.00 | 1 | |
N-nonanoyl-L-Homoserine lactone serves as a pivotal gene regulation reagent by engaging in quorum sensing mechanisms, facilitating intercellular communication among bacterial populations. Its unique lactone structure enables specific interactions with receptor proteins, triggering gene expression changes that influence biofilm formation and virulence. The compound's ability to modulate signaling pathways highlights its role in orchestrating complex biological responses, impacting microbial behavior and community dynamics. | ||||||
Lycorine hydrochloride | 2188-68-3 | sc-200917 sc-200917A | 10 mg 50 mg | $82.00 $310.00 | ||
Lycorine hydrochloride acts as a potent gene regulation reagent by modulating transcriptional activity through its interaction with specific RNA polymerase complexes. This compound influences gene expression by altering chromatin structure and stability, thereby affecting the accessibility of DNA to transcription factors. Its unique ability to disrupt cellular signaling pathways allows for the fine-tuning of gene networks, impacting cellular responses and developmental processes. | ||||||
BML-266 | 96969-83-4 | sc-221371 sc-221371A | 10 mg 50 mg | $170.00 $653.00 | 1 | |
BML-266 serves as a versatile gene regulation reagent, primarily by targeting and inhibiting specific transcription factors. Its unique molecular interactions facilitate the alteration of epigenetic marks, leading to changes in gene accessibility and expression. By modulating key signaling pathways, BML-266 influences the dynamics of gene networks, enabling precise control over cellular processes. This compound's distinct kinetic profile enhances its efficacy in regulating gene expression at multiple levels. | ||||||
BML-210 | 537034-17-6 | sc-221369 sc-221369A | 1 mg 5 mg | $90.00 $272.00 | ||
BML-210 is a potent gene regulation reagent that operates through selective modulation of chromatin remodeling complexes. Its unique ability to disrupt protein-protein interactions allows for the reconfiguration of nucleosome positioning, thereby influencing transcriptional activity. The compound exhibits a distinctive affinity for specific histone modifications, promoting alterations in gene expression patterns. Additionally, BML-210's rapid reaction kinetics enable swift adjustments in cellular gene regulatory networks, enhancing its effectiveness in gene modulation. | ||||||