Items 181 to 190 of 496 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Tris, Hydrochloride | 1185-53-1 | sc-216106 sc-216106A sc-216106B | 500 g 1 kg 25 kg | $195.00 $317.00 $4244.00 | 1 | |
Tris, Hydrochloride serves as a crucial buffer in biological systems, maintaining pH stability essential for cellular signaling. Its unique ability to form hydrogen bonds enhances interactions with biomolecules, facilitating enzyme activity and receptor binding. This compound influences ion channel dynamics and modulates protein conformation, thereby affecting signal transduction pathways. Additionally, its role in stabilizing nucleic acids underscores its importance in cellular communication and metabolic regulation. | ||||||
8-Bromoadenosine 3′,5′-cyclic monophosphate | 23583-48-4 | sc-217493B sc-217493 sc-217493A sc-217493C sc-217493D | 25 mg 50 mg 100 mg 250 mg 500 mg | $108.00 $169.00 $295.00 $561.00 $835.00 | 2 | |
8-Bromoadenosine 3',5'-cyclic monophosphate is a potent cell signaling molecule that mimics the action of cyclic AMP, influencing various intracellular pathways. Its brominated structure enhances stability and alters receptor interactions, leading to distinct signaling cascades. This compound plays a crucial role in modulating protein kinase activity, impacting cellular processes such as metabolism and gene transcription. Its unique properties allow for precise regulation of physiological responses in diverse biological systems. | ||||||
n-Octyl-β-D-glucopyranoside | 29836-26-8 | sc-281091 sc-281091A sc-281091B sc-281091C | 500 mg 1 g 5 g 25 g | $36.00 $56.00 $204.00 $305.00 | 1 | |
n-Octyl-β-D-glucopyranoside is a non-ionic surfactant that facilitates cell signaling by disrupting lipid bilayers and enhancing membrane fluidity. Its hydrophobic octyl chain interacts with membrane proteins, promoting conformational changes that activate signaling pathways. This compound can modulate receptor-ligand interactions, influencing downstream effects such as calcium signaling and gene expression. Its unique amphiphilic nature allows for selective membrane permeabilization, impacting cellular communication and response. | ||||||
Maprotiline Hydrochloride | 10347-81-6 | sc-200156 | 1 g | $74.00 | 7 | |
Maprotiline Hydrochloride acts as a modulator of neurotransmitter signaling, particularly influencing the reuptake of norepinephrine and serotonin. Its unique structure allows it to interact with specific transport proteins, altering synaptic concentrations of these neurotransmitters. This interaction initiates a series of downstream signaling events, affecting neuronal excitability and synaptic plasticity. The compound's kinetic profile reveals distinct binding affinities, contributing to its regulatory role in cellular communication pathways. | ||||||
α-Bungarotoxin | 11032-79-4 | sc-202897 | 1 mg | $351.00 | 5 | |
α-Bungarotoxin is a potent neurotoxin that selectively binds to nicotinic acetylcholine receptors, inhibiting synaptic transmission. Its high affinity for these receptors disrupts normal cell signaling by preventing acetylcholine from eliciting a response, leading to paralysis in affected cells. The toxin's unique interaction alters ion channel dynamics, influencing membrane potential and cellular excitability. This specificity in receptor binding highlights its role in modulating synaptic activity and neuronal communication. | ||||||
Lucifer Yellow CH dipotassium salt | 71206-95-6 | sc-215268 sc-215268A | 25 mg 100 mg | $114.00 $322.00 | 1 | |
Lucifer Yellow CH dipotassium salt is a fluorescent dye that facilitates cell signaling by enabling visualization of cellular processes. Its unique ability to permeate cell membranes allows it to label live cells, highlighting dynamic interactions. The dye exhibits specific binding to cellular components, enhancing contrast in imaging studies. Its fluorescence properties are sensitive to environmental changes, making it a valuable tool for tracking cellular responses and pathways in real-time. | ||||||
Cyclopiazonic Acid | 18172-33-3 | sc-201510 sc-201510A | 10 mg 50 mg | $176.00 $624.00 | 3 | |
Cyclopiazonic Acid is a mycotoxin that disrupts calcium homeostasis by inhibiting the sarcoplasmic reticulum calcium ATPase (SERCA) pump. This interference leads to elevated intracellular calcium levels, triggering aberrant cell signaling pathways. Its unique ability to modulate calcium ion flux affects various cellular processes, including muscle contraction and neurotransmitter release, ultimately influencing cellular responses and signaling cascades. The compound's interaction with SERCA highlights its role in calcium-mediated signaling dysregulation. | ||||||
1-Aminocyclopropane-1-carboxylic Acid | 22059-21-8 | sc-202393 | 500 mg | $143.00 | 2 | |
1-Aminocyclopropane-1-carboxylic Acid serves as a pivotal signaling molecule in plant physiology, particularly in the regulation of ethylene biosynthesis. It acts as a precursor in the ethylene production pathway, influencing fruit ripening and stress responses. Its unique cyclopropane structure allows for specific interactions with enzymes, facilitating the conversion to ethylene. This compound's role in modulating gene expression and cellular responses underscores its significance in plant growth and development. | ||||||
α-Zearalenol | 36455-72-8 | sc-202388 | 5 mg | $268.00 | 1 | |
α-Zearalenol is a mycotoxin that influences cell signaling through its interaction with estrogen receptors, mimicking natural hormones. This compound binds to the receptor's ligand-binding domain, triggering conformational changes that activate transcriptional pathways. Its unique structure allows for selective modulation of gene expression related to reproductive and metabolic processes. Additionally, α-Zearalenol can alter cellular signaling cascades, impacting cell proliferation and differentiation. | ||||||
DL-threo-PDMP, Hydrochloride | 80938-69-8 | sc-203030 | 50 mg | $270.00 | 1 | |
DL-threo-PDMP, Hydrochloride is a potent inhibitor of glycosphingolipid synthesis, influencing cell signaling pathways by modulating lipid composition in cellular membranes. Its unique interaction with sphingolipid metabolism alters membrane fluidity and receptor dynamics, impacting signal transduction. The compound exhibits distinct kinetics in disrupting lipid rafts, thereby affecting protein localization and cellular communication, ultimately influencing various cellular responses. | ||||||