Nucleosides and Analogues
Cambridge Isotope Laboratories Guanosine 5-triphosphate ammonium salt (13C10 99%) CP 90% (in solution) 100 umol
Guanosine 5-triphosphate ammonium salt (13C10 99%) CP 90% (in solution) 100 umol
Medchemexpress LLC ATP dipotassium | 42373-41-1 | 98.7% | 100 MG
ATP dipotassium (Adenosine 5'-triphosphate dipotassium) is a vital molecule for energy storage and metabolism in living organisms. It supplies the metabolic energy required to power metabolic pumps and acts as a coenzyme within cells. This compound also plays a crucial role as an endogenous signaling molecule in immunity and inflammation, making it valuable for a wide range of research applications.
- Supports energy storage and metabolism.
- Drives metabolic pumps and acts as a coenzyme.
- Functions as an endogenous signaling molecule in immunity and inflammation.
- Synergistic effect on NLRP3 inflammasome activation with LPS.
- Induces secretion of IL-1β, KC, and MIP-2 from BMDMs.
- Promotes neutrophil chemotaxis.
- Offers protection against bacterial infection in vivo.
- Induces IL-1β, KC, MIP-2 secretion and neutrophil recruitment in vivo.
Medchemexpress LLC Adenosine 5'-diphosphoribose sodium | 68414-18-6 | MFCD00136017 | 99.5% | 581.30 g·mol⁻1 | C15H22N5NaO14P2 | 1 ML
Adenosine 5′-diphosphoribose sodium is supplied as a ready-to-use aqueous solution (10 mM, 1 mL) for biochemical research. It functions as an ADP-ribose reagent and metabolite standard for studies of NAD+ metabolism and ADP-ribosylation, and is characterized by high reported purity and defined storage recommendations.
- Ready-to-use 10 mM solution in water, 1 mL.
- Approximately 99.5% purity.
- Molecular weight 581.30 g·mol⁻1.
- CAS number 68414-18-6 for unambiguous identification.
- Suitable as a biochemical reagent and metabolite standard in NAD+ and ADP-ribosylation research.
- Storage recommended at -80°C in solution for long-term stability.
Apexbio Technology LLC 2'-O-Methyl-2-Amino-ATP 50ul (100 mM)
2p-O-Methyl-2-Amino-ATP is a modified nucleoside triphosphate incorporating methylation at the ribose 2 -hydroxyl group and an amino substitution at the 2 position of the adenine base It is designed to alter nucleotide biochemical properties impacting RNA stability and structure upon enzymatic incorporation In in vitro transcription assays 2p-O-Methyl-2-Amino-ATP demonstrates an ability to increase RNA resistance to exonuclease-mediated degradation and induce altered RNA secondary structures Based on these properties 2p-O-Methyl-2-Amino-ATP holds research potential in studies of RNA folding dynamics stability assays RNA-protein interactions and analyses involving chemically modified RNA in biomedical research
Apexbio Technology LLC Adenosine 58-61-7 5g
Adenosine (CAS 58-61-7) is a purine nucleoside consisting of adenine covalently linked to a ribose sugar via a -N9-glycosidic bond Endogenously adenosine modulates cellular signaling through activation of specific G protein-coupled adenosine receptors (A1 A2A A2B and A3) influencing diverse physiological processes such as neurotransmission vasodilation and immune responses In biomedical research adenosine is widely utilized to investigate purinergic signaling pathways cardiac function and the regulation of inflammatory and neuroprotective mechanisms as well as serving as a pharmacological tool in receptor binding and functional assays
Apexbio Technology LLC 2-Amino-ATP(Synonyms: 2-NH2-ATP, 2-Aminoadenosine triphosphate, 2-Amino-adenosine-5'-triphosphate, 2-Amino-ATP (free acid)), 50ul (100 mM).
2-Amino-ATP is a modified nucleotide structurally related to ATP (adenosine triphosphate) featuring an amino substitution at the adenine ring s 2-position It acts as an ATP analog capable of competitively binding at the active sites of ATP-dependent enzymes potentially modulating their enzymatic activity and influencing downstream signaling pathways In research settings 2-Amino-ATP serves as a molecular tool to examine substrate specificity mechanistic aspects of ATP-binding enzymes (e g kinases and ATPases) and nucleotide-dependent receptor interactions facilitating studies of nucleotide signaling and cellular metabolism