Cell-permeable cAMP analog that has greater resistance to phosphodiesterases than cAMP. Preferentially activates protein kinase A (PKA). Directly activates Epac, a Rap1 guanine-nucleotide exchange factor.
Cell-permeable cAMP analog that is more resistant to phosphodiesterases than cAMP. Preferentially activates cAMP-dependent protein kinase (PKA). Induces the guanine-nucleotide-exchange factor activity of GEFI, also known as Epac (exchange protein directly activated by cAMP), and GEFII toward Rap1 both in vivo and in vitro.
生物化学的/生理学的作用
Cell permeable: yes
Primary Target PKA
Product does not compete with ATP.
Reversible: no
警告
Toxicity: Standard Handling (A)
再構成
Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C. Avoid pH >8.5.
その他情報
Kawasaki, H., et al. 1998. Science 282, 2275. de Rooij, J., et al. 1998. Nature 396, 474. Boyer, B., and Thiery, J.P. 1993. J. Cell Biol.120, 767. Hei, Y.-J., et al. 1991. Mol. Pharmacol. 39, 233.
法的情報
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany