Items 91 to 100 of 113 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
UNC 926 hydrochloride | 1184136-10-4 | sc-397061 | 10 mg | $159.00 | ||
UNC 926 hydrochloride functions as a potent gene regulation reagent by selectively targeting epigenetic modifiers. Its unique structure allows for specific interactions with histone proteins, leading to alterations in chromatin accessibility. This compound can influence the recruitment of transcriptional co-factors, thereby modulating gene expression. Furthermore, its stability in various cellular environments enhances its efficacy in manipulating gene regulatory mechanisms, making it a valuable tool for studying transcriptional control. | ||||||
I-BET 151 Hydrochloride | 1300031-49-5 (non HCl Salt) | sc-391115 | 10 mg | $450.00 | 2 | |
I-BET 151 Hydrochloride serves as a specialized gene regulation reagent by inhibiting the bromodomain and extraterminal (BET) family of proteins. This selective inhibition disrupts the binding of BET proteins to acetylated lysines on histones, thereby influencing chromatin dynamics. Its unique ability to modulate protein-protein interactions within transcriptional complexes allows for precise control over gene expression pathways, facilitating in-depth studies of epigenetic regulation. | ||||||
L-Ascorbic acid 2-phosphate sesquimagnesium salt | 113170-55-1 | sc-228390 sc-228390A sc-228390B sc-228390C sc-228390D sc-228390E sc-228390F | 5 g 25 g 100 g 500 g 1 kg 5 kg 10 kg | $65.00 $255.00 $520.00 $915.00 $1799.00 $8724.00 $16320.00 | 6 | |
L-Ascorbic acid 2-phosphate sesquimagnesium salt acts as a potent gene regulation reagent by enhancing the stability and bioavailability of ascorbic acid in cellular environments. Its unique phosphate group facilitates specific interactions with transcription factors, promoting the activation of genes involved in antioxidant defense and cellular signaling pathways. This compound's ability to modulate redox states and influence gene expression dynamics makes it a valuable tool for exploring gene regulatory mechanisms. | ||||||
Dimethyl fumarate | 624-49-7 | sc-239774 | 25 g | $27.00 | 6 | |
Dimethyl fumarate serves as a versatile gene regulation reagent by influencing cellular signaling pathways through its unique electrophilic properties. It interacts with thiol groups in proteins, leading to the modulation of redox-sensitive transcription factors. This compound can induce the expression of genes associated with cellular stress responses and inflammation, thereby altering gene expression profiles. Its ability to engage in Michael addition reactions enhances its role in epigenetic modifications and chromatin remodeling. | ||||||
Phytic acid dipotassium salt | 129832-03-7 | sc-253276 sc-253276A | 5 g 25 g | $229.00 $473.00 | 1 | |
Phytic acid dipotassium salt acts as a potent gene regulation reagent by chelating metal ions, which can influence various signaling pathways. Its unique ability to bind to transcription factors alters their activity, impacting gene expression related to metabolic processes. Additionally, it plays a role in modulating the activity of enzymes involved in epigenetic regulation, thereby affecting chromatin structure and gene accessibility. This compound's interactions with cellular components highlight its significance in gene regulation mechanisms. | ||||||
Lys-Tyr-Lys acetate salt | 35193-18-1 | sc-300944 | 50 mg | $163.00 | ||
Lys-Tyr-Lys acetate salt serves as a versatile gene regulation reagent, exhibiting unique interactions with nucleic acids and proteins. Its structure allows for specific binding to regulatory elements, influencing transcriptional activity. The compound can modulate protein-protein interactions, thereby affecting signaling cascades and gene expression patterns. Additionally, its acetate moiety enhances solubility and stability, facilitating its role in cellular environments and promoting effective gene modulation. | ||||||
GW6471 | 880635-03-0 | sc-300779 | 5 mg | $289.00 | 9 | |
GW6471 is a selective antagonist that modulates gene expression through its interaction with nuclear receptors. It specifically inhibits the activity of peroxisome proliferator-activated receptors (PPARs), influencing lipid metabolism and inflammatory pathways. The compound's unique binding affinity alters receptor conformation, impacting downstream signaling cascades. Its stability in various cellular conditions allows for precise manipulation of gene regulation, making it a valuable tool in molecular biology research. | ||||||
N-decanoyl-L-Homoserine lactone | 177315-87-6 | sc-222001 sc-222001A sc-222001B sc-222001C | 5 mg 10 mg 25 mg 50 mg | $88.00 $170.00 $390.00 $640.00 | ||
N-decanoyl-L-Homoserine lactone is a signaling molecule that plays a crucial role in quorum sensing, facilitating communication among bacterial populations. Its unique lactone structure allows for specific interactions with receptor proteins, triggering gene expression changes that regulate biofilm formation and virulence factors. The compound's ability to diffuse across membranes enhances its reactivity and influence on cellular pathways, making it a significant player in microbial gene regulation. | ||||||
N-tridecanoyl-L-Homserine lactone | 878627-21-5 | sc-204812 sc-204812A | 5 mg 10 mg | $40.00 $103.00 | ||
N-tridecanoyl-L-Homoserine lactone is a key regulator in bacterial gene expression, particularly in quorum sensing mechanisms. Its long hydrophobic tail enhances membrane permeability, allowing for efficient cellular uptake and interaction with specific transcriptional regulators. This compound modulates gene networks involved in biofilm development and pathogenicity, influencing bacterial behavior through precise molecular recognition and signaling cascades that alter gene transcription dynamics. | ||||||
13(S)-HODE-d4 | 139408-39-2 | sc-205006 sc-205006A sc-205006B sc-205006C | 25 µg 100 µg 500 µg 1 mg | $112.00 $405.00 $4500.00 $8500.00 | ||
13(S)-HODE-d4 is a specialized gene regulation reagent that engages with lipid signaling pathways, influencing cellular responses through its unique molecular interactions. This compound is known for its role in modulating the activity of peroxisome proliferator-activated receptors (PPARs), which are crucial for regulating metabolic processes. Its distinct isotopic labeling allows for precise tracking in biological systems, enhancing the understanding of gene expression dynamics and cellular signaling mechanisms. | ||||||