- USE - Measure cAMP in 2 hours
- SAMPLE - Lysates, Urine, Plasma, Saliva, Tissue
- SAMPLES/KIT - 38 or 230 in Duplicate
- SENSITIVITY - Measure < 1 fmol cAMP per sample
- STABILITY - Stable 4˚C Liquid Reagents
The DetectX® Cyclic AMP (cAMP) Chemiluminescent Direct Immunoassay (CLIA) kits are designed to quantitatively measure cAMP present in cell lysates, plasma, urine, saliva, tissue and culture media samples. The supplied Sample Diluent will lyse cells, stabilize cAMP and stop phosphodiesterase activity. A cAMP standard is provided to generate a standard curve for the assay. The supplied Plate Primer solution is added to the wells of a coated white microtiter plate, followed by standards or diluted samples. A cAMP-peroxidase conjugate is then added to the wells.
The binding reaction is initiated by the addition of a polyclonal antibody to cAMP. After a 2 hour incubation the plate is washed and chemiluminescent substrate is added. The substrate immediately reacts with the bound cAMP-peroxidase conjugate. The generated chemiluminescent glow signal is measured. The concentration of the cAMP in the sample is calculated, after making correction for the dilution.
Cyclic AMP (cAMP) is one of the most important second messengers and a key intracellular regulator. Discovered by Sutherland and Rall in 1957, it functions as a mediator of activity for a number of hormones, including epinephrine, glucagon, and ACTH. Cyclic AMP is produced by the enzyme adenylate cyclase, and the enzyme is activated by the hormones glucagon and adrenaline and by G protein. cAMP decomposition into AMP is catalyzed by the enzyme phosphodiesterase. Other biological actions of cAMP include regulation of innate immune functioning, axon regeneration, cancer, and inflammation.
|Cyclic AMP Direct CLIA Kit, 1 Plate||K019-C1||$325.00||Inquire About This Product|
|Cyclic AMP Direct CLIA Kit, 5 Plate||K019-C5||$1,310.00||Inquire About This Product|
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- 26 December 2014 - cAMP modulation during sheep in vitro oocyte maturation delays progression of meiosis without affecting oocyte parthenogenetic developmental competence
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- 20 March 2014 - Reciprocal bystander effect between α-irradiated macrophage and hepatocyte is mediated by cAMP through a membrane signaling pathway
- 30 December 2013 - Single-Nucleotide Polymorphisms of the Dopamine D2 Receptor Increase Inflammation and Fibrosis in Human Renal Proximal Tubule Cells
- 11 April 2013 - B. anthracis Edema Toxin Increases cAMP Levels and Inhibits Phenylephrine Stimulated Contraction in a Rat Aortic Ring Mode
- 05 April 2013 - Autocrine Regulation of Macrophage Activation via Exocytosis of ATP and Activation of P2Y11 Receptor
- 11 December 2012 - CD36-dependent signaling mediates fatty acid-induced gut release of secretin and cholecystokinin
- 27 September 2012 - CD36 influences myocardial Ca2+ homeostasis and phospholipid metabolism: Conduction anomalies in CD36 deficient mice during fasting.
- 25 August 2012 - (S)-α-Chlorohydrin Inhibits Protein Tyrosine Phosphorylation through Blocking Cyclic AMP - Protein Kinase A Pathway in Spermatozoa