Items 101 to 110 of 113 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
RETRA | 1036069-26-7 | sc-311522 | 5 mg | $115.00 | 1 | |
RETRA is a potent gene regulation reagent that acts through specific interactions with transcription factors, influencing gene expression patterns. Its unique structure facilitates binding to regulatory sites, modulating the activity of various signaling pathways. RETRA's ability to alter chromatin dynamics enhances its role in epigenetic regulation, promoting or repressing target genes. This compound exhibits distinct reaction kinetics, allowing for rapid cellular responses to environmental stimuli. | ||||||
2-Phospho-L-ascorbic acid trisodium salt | 66170-10-3 | sc-230644 sc-230644A | 10 g 25 g | $161.00 $344.00 | ||
2-Phospho-L-ascorbic acid trisodium salt is a potent gene regulation reagent that enhances cellular signaling through its unique interactions with transcription factors. This compound acts as a powerful antioxidant, stabilizing reactive species and influencing gene expression related to oxidative stress responses. Its solubility in aqueous environments facilitates rapid cellular uptake, promoting effective modulation of gene pathways involved in cellular growth and differentiation. | ||||||
2-Bromohexadecanoic acid | 18263-25-7 | sc-251714 sc-251714A | 10 g 50 g | $53.00 $201.00 | 4 | |
2-Bromohexadecanoic acid serves as a versatile gene regulation reagent, exhibiting unique interactions with lipid membranes and protein targets. Its hydrophobic nature allows for effective incorporation into cellular membranes, influencing membrane fluidity and protein localization. This compound can modulate signaling pathways by altering lipid composition, thereby impacting gene expression related to metabolic processes. Its reactivity as an acid halide enables selective modifications of biomolecules, enhancing its role in gene regulation. | ||||||
Pyroxamide | 382180-17-8 | sc-397030 | 5 mg | $79.00 | ||
Pyroxamide functions as a potent gene regulation reagent, characterized by its ability to selectively interact with transcription factors and chromatin remodeling complexes. Its unique structure facilitates binding to specific DNA sequences, influencing gene expression patterns. Additionally, Pyroxamide can alter post-translational modifications of histones, thereby modulating chromatin accessibility. This compound's stability and reactivity allow for targeted modifications, enhancing its efficacy in gene regulation pathways. | ||||||
5-Carboxy-8-hydroxyquinoline | 5852-78-8 | sc-397023 | 5 mg | $86.00 | ||
5-Carboxy-8-hydroxyquinoline serves as a versatile gene regulation reagent, notable for its capacity to chelate metal ions, which can influence enzymatic activity and gene expression. Its unique ability to form stable complexes with transition metals allows it to modulate the activity of metalloproteins involved in transcriptional regulation. Furthermore, this compound can impact cellular signaling pathways by altering the redox state, thereby affecting gene regulatory networks. | ||||||
LG 100754 | 180713-37-5 | sc-361231 sc-361231A | 5 mg 25 mg | $137.00 $555.00 | ||
LG 100754 is a potent gene regulation reagent characterized by its selective inhibition of specific transcription factors. It interacts with target proteins through non-covalent binding, effectively disrupting their function and altering downstream gene expression. This compound exhibits unique kinetics, allowing for rapid modulation of gene activity, and can influence chromatin remodeling processes. Its distinct mechanism of action provides insights into regulatory pathways, making it a valuable tool for studying gene regulation dynamics. | ||||||
N-(Ketocaproyl)-L-homoserine Lactone | 143537-62-6 | sc-207922 | 100 mg | $340.00 | ||
N-(Ketocaproyl)-L-homoserine Lactone serves as a versatile gene regulation reagent, known for its role in modulating quorum sensing pathways. This compound engages in specific molecular interactions with receptor proteins, facilitating the activation or repression of target genes. Its unique structural features enable it to influence signal transduction cascades, thereby affecting cellular responses. The compound's ability to fine-tune gene expression dynamics makes it an essential tool for exploring complex regulatory networks. | ||||||
SAG | 912545-86-9 | sc-212905 sc-212905A | 1 mg 5 mg | $166.00 $421.00 | 27 | |
SAG is a versatile gene regulation reagent that engages in specific interactions with RNA polymerase and associated cofactors. Its unique ability to modify histone acetylation enhances or suppresses transcriptional activity, thereby influencing gene expression dynamics. SAG's distinct chemical properties facilitate its role in chromatin remodeling, allowing for precise control over gene activation and silencing. This compound is essential for exploring the complexities of gene regulatory networks and cellular responses. | ||||||
SID 7969543 | 868224-64-0 | sc-204278 sc-204278A | 10 mg 50 mg | $139.00 $585.00 | ||
SID 7969543 is a potent gene regulation reagent that operates through intricate molecular interactions with transcription factors. Its unique structural motifs allow it to selectively bind to DNA regulatory elements, influencing gene expression patterns. By modulating chromatin accessibility and stability, SID 7969543 can alter the kinetics of transcriptional activation or repression. This compound is instrumental in dissecting cellular signaling pathways and understanding gene regulatory mechanisms. | ||||||
Cardionogen 1 | 577696-37-8 | sc-397033 sc-397033A | 5 mg 25 mg | $140.00 $510.00 | ||
Cardionogen 1 is a specialized gene regulation reagent that selectively binds to transcription factors, modulating their activity through unique conformational changes. Its distinct molecular interactions promote the recruitment of co-activators or co-repressors, influencing chromatin accessibility. The compound's kinetic profile allows for rapid adjustments in gene expression, making it a powerful tool for dissecting regulatory pathways and understanding cellular mechanisms at a molecular level. | ||||||