Two fast and sensitive methods for the determination of cAMP and cGMP levels in mantle tissue of the sea mussel Mytilus galloprovincialis Lmk. are described. Both methods use ion-pair high-performance liquid chromatography with diode array detection. The use of the diode array detector permitted the
Simultaneous isolation of adenosine 3′,5′-cyclic monophosphate (cAMP) and guanosine 3′,5′-cyclic monophosphate (cGMP) in small tissue samples
✍ Scribed by C.C. Mao; A. Guidotti
- Publisher
- Elsevier Science
- Year
- 1974
- Tongue
- English
- Weight
- 348 KB
- Volume
- 59
- Category
- Article
- ISSN
- 0003-2697
No coin nor oath required. For personal study only.
✦ Synopsis
A column chromatogrnphic sy;itrm has been developed for isolation and purification of cAMP and cGMP simultnneously from small tissue samples. In this system, a column of neutral aluminum oxide equilibrated in Tris-HCl buffer, pH 7.5 was used to purify cyclic nucleotides from olhe~ nucleotides in non-cyclic form, Subsequently, CAMP and cGMP are scparakd from each other through a Dowex l-52 column cluted with small volumes of HCl of d&rent molaritics. The elution patterns of both cyclic nuclcotides through the entire purification procedure arc highly reproducible with excellent recovery.
📜 SIMILAR VOLUMES
A possible defect of guanosine 3Ј-5Ј-cyclic monophosphate (cGMP) content in the renal tissue caused by an increased activity of cGMP phosphodiesterase (PDE) has, so far, not been evaluated in the pathogenesis of renal resistance to endogenous natriuretic peptides (ENP) in cirrhosis with ascites. To
## Abstract ## BACKGROUND The 32‐kilodalton dopamine and cyclic adenosine 3′,5′‐monophosphate‐regulated phosphoprotein (DARPP‐32) is the only known protein that can act as a protein phosphatase‐1 inhibitor or a protein kinase inhibitor. It is known as a neurogenic protein that plays a major role i