8- Hydroxyadenosine- 3', 5'- cyclic monophosphorothioate, Sp- isomer (Sp-8-OH-cAMPS) biochemical product blog
Tags: Biochemical; 8- Hydroxyadenosine- 3', 5'- cyclic monophosphorothioate, Sp- isomer (Sp-8-OH-cAMPS); 8- Hydroxyadenosine- 3', 5'- cyclic monophosphorothioate, Sp- isomer (Sp-8-OH-cAMPS) biochemical;
The 8- Hydroxyadenosine- 3\', 5\'- cyclic monophosphorothioate, Sp- isomer (Sp-8-OH-cAMPS) n/a (Catalog #MBS256486) is a Biochemical and is intended for research purposes only. The product is available for immediate purchase.To buy or view more detailed product information and pricing, please click on the technical datasheet page below:
Please refer to the product datasheet for known applications of a given biochemical. We\'ve tested the 8- Hydroxyadenosine- 3\', 5\'- cyclic monophosphorothioate, Sp- isomer (Sp-8-OH-cAMPS) with the following immunoassay(s):
Structure
C10H11N5O6PS.Na; MW 383.3; lambdamax 268 nm; epsilon 11000; sodium salt; purity > 99% HPLC. For other salt forms please inquire. Polar, membrane-impermeant analogue of the protein kinase An activator Sp-cAMPS, e.g. for the study of extracellular cAMP receptors. If applied by patch clamp techniques, Sp-8-OH-cAMPS should remain trapped inside the cell. Highly resistant against mammalian cyclic nucleotide-dependent phosphodiesterases. Detailed technical information available. Reference: Otmakhov & Lisman, J. Neurophysiol., 87, 3018 - 3032 (2002).
Unit Equivalent: 5 umol is approximately equals to 1.9 mg
CAS No.: 749843-87-6. Formula: C10H11N5O6PS.Na.