Assay Principle:

The DetectX hours. Users should thoroughly read the complete kit insert for detailed instructions before performing the assay. The kit includes a PKA Standard to establish an accurate standard curve.

Protocol Summary:

• Add standards or diluted samples in kinase assay buffer to the provided transparent microtiter plate with bound PKA substrate.
• Introduce reconstituted ATP to each well, ensuring proper mixing of reagents.
• Incubate the sealed plate at 30 minutes.
• Add Donkey anti-Rabbit IgG HRP Conjugate and Rabbit Phospho PKA Substrate Antibody to each well. Incubate at room temperature for 60 minutes.
• After incubation, wash away excess phospho-PKA-peroxidase conjugate. Then add the TMB substrate, which reacts with the bound conjugate to generate a detectable signal.
• Use a plate reader to measure the signal at 450nm and calculate PKA activity using the standard curve.

Background:

Protein Kinase A (PKA) is activated when cyclic AMP (cAMP) levels rise following stimulation of G Protein-coupled receptors and adenylyl cyclase. The expressed PKA holoenzyme comprises two catalytic (C) and two regulatory (R) subunits. In its inactive state, the pseudosubstrate sequences on the R subunits inhibit the activity of the C subunits, which are released as active monomers upon cAMP binding to the R subunits. PKA’s localization and interaction with A kinase-anchoring proteins (AKAPs) regulate the phosphorylation of specific substrates, including Bad (Ser155), CREB (Ser133), and GSK-3 (GSK-3α Ser21 and GSK-3β Ser9). PKA shares substrate specificity with Akt (PKB) and PKC.

PKA plays a vital role in various physiological processes, including cancer progression, vasodilation, and metabolic regulation. It is particularly significant in cardiac function and remodeling and shows substantial alterations in signaling in conditions like obesity. The DetectX id="related-products-heading">Related News