Items 31 to 40 of 185 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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D-myo-Inositol-4-phosphate (ammonium salt) | 142760-33-6 | sc-205287 sc-205287A | 100 µg 500 µg | $220.00 $650.00 | ||
D-myo-Inositol-4-phosphate (ammonium salt) is a phosphorylated carbohydrate that plays a pivotal role in cellular signaling pathways. Its unique phosphate group facilitates interactions with various proteins, influencing signal transduction and metabolic processes. The compound exhibits distinct solubility characteristics, allowing it to participate in diverse biochemical reactions. Its structural conformation can modulate enzyme activity, impacting the kinetics of phosphorylation and dephosphorylation events within cellular systems. | ||||||
myo-Inositol | 87-89-8 | sc-202714 sc-202714A sc-202714B sc-202714C | 100 g 250 g 1 kg 5 kg | $78.00 $148.00 $270.00 $821.00 | ||
Myo-Inositol is a cyclic sugar alcohol that serves as a versatile carbohydrate, integral to cellular processes. Its unique stereochemistry allows for multiple hydroxyl groups to engage in hydrogen bonding, enhancing its solubility in aqueous environments. This property facilitates its role in forming phospholipids and inositol phosphates, which are crucial for membrane dynamics and intracellular signaling. Additionally, myo-Inositol's ability to act as a secondary messenger underscores its importance in regulating various metabolic pathways. | ||||||
Trehalose dihydrate, cell culture | 6138-23-4 | sc-394303 sc-394303A sc-394303B | 10 g 25 g 100 g | $76.00 $135.00 $355.00 | 1 | |
Trehalose dihydrate is a disaccharide composed of two glucose units linked by an α,α-1,1-glycosidic bond, exhibiting unique properties in cellular environments. Its ability to form hydrogen bonds contributes to its high solubility and stability, making it an effective osmoprotectant. Trehalose dihydrate influences cellular signaling pathways and stress responses, enhancing cell viability under adverse conditions. Its distinct molecular interactions facilitate the preservation of protein structure and function. | ||||||
DL-Glyceraldehyde 3-phosphate solution | 591-59-3 (free acid) | sc-507252 | 25 mg | $221.00 | ||
DL-Glyceraldehyde 3-phosphate is a triose phosphate that serves as a pivotal intermediate in glycolysis and the Calvin cycle. Its aldehyde group allows for rapid oxidation and reduction reactions, facilitating energy transfer within cells. The compound's ability to form stable enolates enhances its reactivity in various biochemical pathways. Additionally, its role in the synthesis of amino acids and nucleotides underscores its importance in metabolic networks, influencing cellular energy dynamics. | ||||||
PLC Thio-PIP2 (sodium salt) | sc-224207 sc-224207A | 100 µg 500 µg | $188.00 $846.00 | |||
PLC Thio-PIP2 (sodium salt) is a sophisticated carbohydrate derivative known for its unique thiophosphate group, which enhances its reactivity and interaction with biological macromolecules. This compound exhibits distinct binding affinities, influencing cellular signaling pathways and modulating enzyme activities. Its structural flexibility allows for dynamic conformational changes, facilitating interactions with lipid membranes and contributing to its role in cellular communication and metabolic regulation. | ||||||
Gum guaiac | 9000-29-7 | sc-215116B sc-215116 sc-215116A | 25 g 1 kg 100 g | $82.00 $1574.00 $305.00 | ||
Gum guaiac is a complex carbohydrate known for its unique structural properties, including its ability to form hydrogen bonds and engage in hydrophobic interactions. These characteristics contribute to its solubility in organic solvents and its role in stabilizing various molecular structures. The compound's intricate polymerization pathways allow for diverse interactions within biological systems, influencing its reactivity and participation in metabolic processes. Its distinct physical properties, such as viscosity and texture, further enhance its functional versatility. | ||||||
Phytic acid calcium salt | 23183-60-0 | sc-253275 sc-253275A | 5 g 25 g | $220.00 $925.00 | ||
Phytic acid calcium salt is notable for its ability to chelate metal ions, forming stable complexes that influence nutrient bioavailability. Its unique structure allows for multiple phosphate groups to engage in electrostatic interactions, enhancing its solubility in aqueous environments. This compound also participates in various biochemical pathways, modulating enzymatic activities and influencing metabolic processes. Its distinct physical properties, such as viscosity and texture, further affect its behavior in different systems. | ||||||
N-Acetyl-α-D-glucosamine 1-phosphate disodium salt | 31281-59-1 | sc-215434 sc-215434A | 5 mg 25 mg | $260.00 $650.00 | ||
N-Acetyl-α-D-glucosamine 1-phosphate disodium salt exhibits unique properties as a carbohydrate, particularly in its role as a substrate in glycosylation reactions. Its phosphorylated structure enhances its reactivity, facilitating interactions with enzymes and other biomolecules. This compound can influence cellular signaling pathways through its participation in the synthesis of glycoproteins and glycolipids, impacting cellular communication and structural integrity. Its solubility and stability in physiological conditions further contribute to its functional versatility in biological systems. | ||||||
IPTG, Dioxane-Free | 367-93-1 | sc-202185 sc-202185A sc-202185B sc-202185C sc-202185D sc-202185E sc-202185F | 1 g 5 g 100 g 500 g 1 kg 10 kg 25 kg | $50.00 $115.00 $500.00 $1750.00 $2000.00 $16320.00 $32130.00 | 27 | |
IPTG, dioxane-free, is a synthetic compound that acts as a potent inducer of gene expression by mimicking lactose. Its unique structure facilitates specific interactions with the lac repressor protein, effectively releasing it from the operator site on DNA. This interaction initiates transcriptional activation, leading to enhanced protein production. The compound's stability and solubility in aqueous environments contribute to its effectiveness in promoting controlled gene expression in various biological systems. | ||||||
2,7-Dimethyloctane | 1072-16-8 | sc-266238 | 1 g | $47.00 | ||
2,7-Dimethyloctane is a branched alkane characterized by its unique hydrophobic interactions, which influence its behavior in various chemical environments. Its structure allows for distinct packing in liquid phases, affecting viscosity and diffusion rates. The compound's non-polar nature leads to minimal solubility in polar solvents, impacting its reactivity in organic synthesis. Additionally, its steric hindrance can influence reaction pathways, making it a subject of interest in studies of hydrocarbon behavior. |